TCF7L2 (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "TCF7L2" in English language version.

refsWebsite

Global rank English rank

82nih.gov

4^th place

46doi.org

2^nd place

7semanticscholar.org

11^th place

8^th place

6harvard.edu

18^th place

17^th place

2ensembl.org

1,626^th place

1,007^th place

1omim.org

4,380^th place

4,305^th place

1handle.net

102^nd place

76^th place

1rcsb.org

8,838^th place

8,783^rd place

1genecards.org

low place

1uniprot.org

5,673^rd place

6,418^th place

1sfari.org

low place

1mousephenotype.org

low place

1immunophenotyping.org

low place

1marrvel.org

low place

doi.org (Global: 2^nd place; English: 2^nd place)

Castrop J, van Norren K, Clevers H (February 1992). "A gene family of HMG-box transcription factors with homology to TCF-1". Nucleic Acids Research. 20 (3): 611. doi:10.1093/nar/20.3.611. PMC 310434. PMID 1741298.
Jin T, Liu L (November 2008). "The Wnt signaling pathway effector TCF7L2 and type 2 diabetes mellitus". Molecular Endocrinology. 22 (11): 2383–2392. doi:10.1210/me.2008-0135. PMID 18599616.
Zhang C, Bao W, Rong Y, Yang H, Bowers K, Yeung E, et al. (2013-05-19). "Genetic variants and the risk of gestational diabetes mellitus: a systematic review". Human Reproduction Update. 19 (4): 376–390. doi:10.1093/humupd/dmt013. PMC 3682671. PMID 23690305.
Fitzgerald TW, Gerety SS, Jones WD, Van Kogelenberg M, King DA, McRae J, et al. (Deciphering Developmental Disorders Study) (March 2015). "Large-scale discovery of novel genetic causes of developmental disorders". Nature. 519 (7542): 223–228. Bibcode:2015Natur.519..223T. doi:10.1038/nature14135. PMC 5955210. PMID 25533962.
Clayton S, Fitzgerald TW, Kaplanis J, Prigmore E, Rajan D, Sifrim A, et al. (Deciphering Developmental Disorders Study) (February 2017). "Prevalence and architecture of de novo mutations in developmental disorders". Nature. 542 (7642): 433–438. Bibcode:2017Natur.542..433M. doi:10.1038/nature21062. PMC 6016744. PMID 28135719.
Hansen T, Ingason A, Djurovic S, Melle I, Fenger M, Gustafsson O, et al. (July 2011). "At-risk variant in TCF7L2 for type II diabetes increases risk of schizophrenia". Biological Psychiatry. 70 (1): 59–63. doi:10.1016/j.biopsych.2011.01.031. PMID 21414605. S2CID 42205809.
Liu L, Li J, Yan M, Li J, Chen J, Zhang Y, et al. (April 2017). "TCF7L2 polymorphisms and the risk of schizophrenia in the Chinese Han population". Oncotarget. 8 (17): 28614–28620. doi:10.18632/oncotarget.15603. PMC 5438676. PMID 28404897.
Wang T, Hoekzema K, Vecchio D, Wu H, Sulovari A, Coe BP, et al. (October 2020). "Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders". Nature Communications. 11 (1) 4932. Bibcode:2020NatCo..11.4932W. doi:10.1038/s41467-020-18723-y. PMC 7530681. PMID 33004838.
Satterstrom FK, Kosmicki JA, Wang J, Breen MS, De Rubeis S, An JY, et al. (February 2020). "Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism". Cell. 180 (3): 568–584.e23. doi:10.1016/j.cell.2019.12.036. PMC 7250485. PMID 31981491.
Torres S, García-Palmero I, Marín-Vicente C, Bartolomé RA, Calviño E, Fernández-Aceñero MJ, et al. (January 2018). "Proteomic Characterization of Transcription and Splicing Factors Associated with a Metastatic Phenotype in Colorectal Cancer". Journal of Proteome Research. 17 (1): 252–264. doi:10.1021/acs.jproteome.7b00548. hdl:10261/160082. PMID 29131639.
Vallée A, Vallée JN, Guillevin R, Lecarpentier Y (May 2018). "Interactions Between the Canonical WNT/Beta-Catenin Pathway and PPAR Gamma on Neuroinflammation, Demyelination, and Remyelination in Multiple Sclerosis". Cellular and Molecular Neurobiology. 38 (4): 783–795. doi:10.1007/s10571-017-0550-9. PMC 11482031. PMID 28905149. S2CID 4620853.
Vaquero AR, Ferreira NE, Omae SV, Rodrigues MV, Teixeira SK, Krieger JE, et al. (October 2012). "Using gene-network landscape to dissect genotype effects of TCF7L2 genetic variant on diabetes and cardiovascular risk". Physiological Genomics. 44 (19): 903–914. doi:10.1152/physiolgenomics.00030.2012. PMID 22872755. S2CID 35065699.
PDB: 2GL7; Sampietro J, Dahlberg CL, Cho US, Hinds TR, Kimelman D, Xu W (October 2006). "Crystal structure of a beta-catenin/BCL9/Tcf4 complex". Molecular Cell. 24 (2): 293–300. doi:10.1016/j.molcel.2006.09.001. PMID 17052462.
Lee JM, Dedhar S, Kalluri R, Thompson EW (March 2006). "The epithelial-mesenchymal transition: new insights in signaling, development, and disease". The Journal of Cell Biology. 172 (7): 973–981. doi:10.1083/jcb.200601018. PMC 2063755. PMID 16567498.
Facchinello N, Tarifeño-Saldivia E, Grisan E, Schiavone M, Peron M, Mongera A, et al. (August 2017). "Tcf7l2 plays pleiotropic roles in the control of glucose homeostasis, pancreas morphology, vascularization and regeneration". Scientific Reports. 7 (1) 9605. Bibcode:2017NatSR...7.9605F. doi:10.1038/s41598-017-09867-x. PMC 5575064. PMID 28851992.
Lipiec MA, Bem J, Koziński K, Chakraborty C, Urban-Ciećko J, Zajkowski T, et al. (August 2020). "TCF7L2 regulates postmitotic differentiation programmes and excitability patterns in the thalamus". Development. 147 (16) dev.190181. doi:10.1242/dev.190181 (inactive 13 November 2025). PMC 7473649. PMID 32675279.{{cite journal}}: CS1 maint: DOI inactive as of November 2025 (link)
Chen Y, Zhao Y, Li YB, Wang YJ, Zhang GZ (January 2018). "Detection of SNPs of T2DM susceptibility genes by a ligase detection reaction-fluorescent nanosphere technique". Analytical Biochemistry. 540–541 (Supplement C): 38–44. doi:10.1016/j.ab.2017.11.003. PMID 29128291.
Zhu L, Xie Z, Lu J, Hao Q, Kang M, Chen S, et al. (September 2017). "TCF7L2 rs290481 T>C polymorphism is associated with an increased risk of type 2 diabetes mellitus and fasting plasma glucose level". Oncotarget. 8 (44): 77000–77008. doi:10.18632/oncotarget.20300. PMC 5652758. PMID 29100364.
Nagalski A, Irimia M, Szewczyk L, Ferran JL, Misztal K, Kuznicki J, et al. (November 2013). "Postnatal isoform switch and protein localization of LEF1 and TCF7L2 transcription factors in cortical, thalamic, and mesencephalic regions of the adult mouse brain". Brain Structure & Function. 218 (6): 1531–1549. doi:10.1007/s00429-012-0474-6. PMC 3825142. PMID 23152144.
Murray KD, Rubin CM, Jones EG, Chalupa LM (November 2008). "Molecular correlates of laminar differences in the macaque dorsal lateral geniculate nucleus". The Journal of Neuroscience. 28 (46): 12010–12022. doi:10.1523/JNEUROSCI.3800-08.2008. PMC 2613947. PMID 19005066.
Nobrega MA (March 2013). "TCF7L2 and glucose metabolism: time to look beyond the pancreas". Diabetes. 62 (3): 706–708. doi:10.2337/db12-1418. PMC 3581232. PMID 23431017.
Duggirala R, Blangero J, Almasy L, Dyer TD, Williams KL, Leach RJ, et al. (April 1999). "Linkage of type 2 diabetes mellitus and of age at onset to a genetic location on chromosome 10q in Mexican Americans". American Journal of Human Genetics. 64 (4): 1127–1140. doi:10.1086/302316. PMC 1377837. PMID 10090898.
Grant SF, Thorleifsson G, Reynisdottir I, Benediktsson R, Manolescu A, Sainz J, et al. (March 2006). "Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes". Nature Genetics. 38 (3): 320–323. doi:10.1038/ng1732. PMID 16415884. S2CID 28825825.
Jin T (June 2016). "Current Understanding on Role of the Wnt Signaling Pathway Effector TCF7L2 in Glucose Homeostasis". Endocrine Reviews. 37 (3): 254–277. doi:10.1210/er.2015-1146. PMID 27159876.
Slattery ML, Folsom AR, Wolff R, Herrick J, Caan BJ, Potter JD (April 2008). "Transcription factor 7-like 2 polymorphism and colon cancer". Cancer Epidemiology, Biomarkers & Prevention. 17 (4): 978–982. doi:10.1158/1055-9965.EPI-07-2687. PMC 2587179. PMID 18398040.
Hazra A, Fuchs CS, Chan AT, Giovannucci EL, Hunter DJ (November 2008). "Association of the TCF7L2 polymorphism with colorectal cancer and adenoma risk". Cancer Causes & Control. 19 (9): 975–980. doi:10.1007/s10552-008-9164-3. PMC 2719293. PMID 18478343.
Tang W, Dodge M, Gundapaneni D, Michnoff C, Roth M, Lum L (July 2008). "A genome-wide RNAi screen for Wnt/beta-catenin pathway components identifies unexpected roles for TCF transcription factors in cancer". Proceedings of the National Academy of Sciences of the United States of America. 105 (28): 9697–9702. Bibcode:2008PNAS..105.9697T. doi:10.1073/pnas.0804709105. PMC 2453074. PMID 18621708.
Sun P, Xiong H, Kim TH, Ren B, Zhang Z (February 2006). "Positive inter-regulation between beta-catenin/T cell factor-4 signaling and endothelin-1 signaling potentiates proliferation and survival of prostate cancer cells". Molecular Pharmacology. 69 (2): 520–531. doi:10.1124/mol.105.019620. PMID 16291872. S2CID 10148857.
Beretta CA, Dross N, Bankhead P, Carl M (September 2013). "The ventral habenulae of zebrafish develop in prosomere 2 dependent on Tcf7l2 function". Neural Development. 8 (1) 19. doi:10.1186/1749-8104-8-19. PMC 3827927. PMID 24067090.
Hüsken U, Stickney HL, Gestri G, Bianco IH, Faro A, Young RM, et al. (October 2014). "Tcf7l2 is required for left-right asymmetric differentiation of habenular neurons". Current Biology. 24 (19): 2217–2227. Bibcode:2014CBio...24.2217H. doi:10.1016/j.cub.2014.08.006. PMC 4194317. PMID 25201686.
Vacik T, Stubbs JL, Lemke G (September 2011). "A novel mechanism for the transcriptional regulation of Wnt signaling in development". Genes & Development. 25 (17): 1783–1795. doi:10.1101/gad.17227011. PMC 3175715. PMID 21856776.
Chodelkova O, Masek J, Korinek V, Kozmik Z, Machon O (May 2018). "Tcf7L2 is essential for neurogenesis in the developing mouse neocortex". Neural Development. 13 (1) 8. doi:10.1186/s13064-018-0107-8. PMC 5946422. PMID 29751817.
Lee M, Yoon J, Song H, Lee B, Lam DT, Yoon J, et al. (April 2017). "Tcf7l2 plays crucial roles in forebrain development through regulation of thalamic and habenular neuron identity and connectivity". Developmental Biology. 424 (1): 62–76. doi:10.1016/j.ydbio.2017.02.010. PMID 28219675.
de Zwarte SM, Brouwer RM, Tsouli A, Cahn W, Hillegers MH, Hulshoff Pol HE, et al. (October 2019). "Running in the Family? Structural Brain Abnormalities and IQ in Offspring, Siblings, Parents, and Co-twins of Patients with Schizophrenia". Schizophrenia Bulletin. 45 (6): 1209–1217. doi:10.1093/schbul/sby182. PMC 6811835. PMID 30597053.
Giraldo-Chica M, Woodward ND (February 2017). "Review of thalamocortical resting-state fMRI studies in schizophrenia". Schizophrenia Research. Pathologies of the Thalamus in Schizophrenia. 180: 58–63. doi:10.1016/j.schres.2016.08.005. PMC 5297399. PMID 27531067.
Hua J, Blair NI, Paez A, Choe A, Barber AD, Brandt A, et al. (April 2019). "Altered functional connectivity between sub-regions in the thalamus and cortex in schizophrenia patients measured by resting state BOLD fMRI at 7T". Schizophrenia Research. 206: 370–377. doi:10.1016/j.schres.2018.10.016. PMC 6500777. PMID 30409697.
van Erp TG, Walton E, Hibar DP, Schmaal L, Jiang W, Glahn DC, et al. (November 2018). "Cortical Brain Abnormalities in 4474 Individuals With Schizophrenia and 5098 Control Subjects via the Enhancing Neuro Imaging Genetics Through Meta Analysis (ENIGMA) Consortium". Biological Psychiatry. 84 (9): 644–654. doi:10.1016/j.biopsych.2018.04.023. PMC 6177304. PMID 29960671.
Ayub R, Sun KL, Flores RE, Lam VT, Jo B, Saggar M, et al. (February 2021). "Thalamocortical connectivity is associated with autism symptoms in high-functioning adults with autism and typically developing adults". Translational Psychiatry. 11 (1) 93. doi:10.1038/s41398-021-01221-0. PMC 7859407. PMID 33536431.
Schuetze M, Park MT, Cho IY, MacMaster FP, Chakravarty MM, Bray SL (October 2016). "Morphological Alterations in the Thalamus, Striatum, and Pallidum in Autism Spectrum Disorder". Neuropsychopharmacology. 41 (11): 2627–2637. doi:10.1038/npp.2016.64. PMC 5026732. PMID 27125303.
Tomasi D, Volkow ND (February 2019). "Reduced Local and Increased Long-Range Functional Connectivity of the Thalamus in Autism Spectrum Disorder". Cerebral Cortex. 29 (2): 573–585. doi:10.1093/cercor/bhx340. PMC 6319176. PMID 29300843.
Woodward ND, Giraldo-Chica M, Rogers B, Cascio CJ (January 2017). "Thalamocortical dysconnectivity in autism spectrum disorder: An analysis of the Autism Brain Imaging Data Exchange". Biological Psychiatry. Cognitive Neuroscience and Neuroimaging. 2 (1): 76–84. doi:10.1016/j.bpsc.2016.09.002. PMC 5455796. PMID 28584881.
Gerdin AK (2010). "The Sanger Mouse Genetics Programme: high throughput characterisation of knockout mice". Acta Ophthalmologica. 88: 925–7. doi:10.1111/j.1755-3768.2010.4142.x. S2CID 85911512.
Skarnes WC, Rosen B, West AP, Koutsourakis M, Bushell W, Iyer V, et al. (June 2011). "A conditional knockout resource for the genome-wide study of mouse gene function". Nature. 474 (7351): 337–342. doi:10.1038/nature10163. PMC 3572410. PMID 21677750.
Dolgin E (June 2011). "Mouse library set to be knockout". Nature. 474 (7351): 262–263. doi:10.1038/474262a. PMID 21677718.
Collins FS, Rossant J, Wurst W (January 2007). "A mouse for all reasons". Cell. 128 (1): 9–13. doi:10.1016/j.cell.2006.12.018. PMID 17218247. S2CID 18872015.
White JK, Gerdin AK, Karp NA, Ryder E, Buljan M, Bussell JN, et al. (July 2013). "Genome-wide generation and systematic phenotyping of knockout mice reveals new roles for many genes". Cell. 154 (2): 452–464. doi:10.1016/j.cell.2013.06.022. PMC 3717207. PMID 23870131.

ensembl.org (Global: 1,626^th place; English: 1,007^th place)

May2017.archive.ensembl.org

GRCh38: Ensembl release 89: ENSG00000148737 – Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000024985 – Ensembl, May 2017

genecards.org (Global: low place; English: low place)

"TCF7L2 Gene - GeneCards | TF7L2 Protein | TF7L2 Antibody". GeneCards Human Gene Database. Retrieved 2017-11-30.

handle.net (Global: 102^nd place; English: 76^th place)

hdl.handle.net

Torres S, García-Palmero I, Marín-Vicente C, Bartolomé RA, Calviño E, Fernández-Aceñero MJ, et al. (January 2018). "Proteomic Characterization of Transcription and Splicing Factors Associated with a Metastatic Phenotype in Colorectal Cancer". Journal of Proteome Research. 17 (1): 252–264. doi:10.1021/acs.jproteome.7b00548. hdl:10261/160082. PMID 29131639.

harvard.edu (Global: 18^th place; English: 17^th place)

ui.adsabs.harvard.edu

Fitzgerald TW, Gerety SS, Jones WD, Van Kogelenberg M, King DA, McRae J, et al. (Deciphering Developmental Disorders Study) (March 2015). "Large-scale discovery of novel genetic causes of developmental disorders". Nature. 519 (7542): 223–228. Bibcode:2015Natur.519..223T. doi:10.1038/nature14135. PMC 5955210. PMID 25533962.
Clayton S, Fitzgerald TW, Kaplanis J, Prigmore E, Rajan D, Sifrim A, et al. (Deciphering Developmental Disorders Study) (February 2017). "Prevalence and architecture of de novo mutations in developmental disorders". Nature. 542 (7642): 433–438. Bibcode:2017Natur.542..433M. doi:10.1038/nature21062. PMC 6016744. PMID 28135719.
Wang T, Hoekzema K, Vecchio D, Wu H, Sulovari A, Coe BP, et al. (October 2020). "Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders". Nature Communications. 11 (1) 4932. Bibcode:2020NatCo..11.4932W. doi:10.1038/s41467-020-18723-y. PMC 7530681. PMID 33004838.
Facchinello N, Tarifeño-Saldivia E, Grisan E, Schiavone M, Peron M, Mongera A, et al. (August 2017). "Tcf7l2 plays pleiotropic roles in the control of glucose homeostasis, pancreas morphology, vascularization and regeneration". Scientific Reports. 7 (1) 9605. Bibcode:2017NatSR...7.9605F. doi:10.1038/s41598-017-09867-x. PMC 5575064. PMID 28851992.
Tang W, Dodge M, Gundapaneni D, Michnoff C, Roth M, Lum L (July 2008). "A genome-wide RNAi screen for Wnt/beta-catenin pathway components identifies unexpected roles for TCF transcription factors in cancer". Proceedings of the National Academy of Sciences of the United States of America. 105 (28): 9697–9702. Bibcode:2008PNAS..105.9697T. doi:10.1073/pnas.0804709105. PMC 2453074. PMID 18621708.
Hüsken U, Stickney HL, Gestri G, Bianco IH, Faro A, Young RM, et al. (October 2014). "Tcf7l2 is required for left-right asymmetric differentiation of habenular neurons". Current Biology. 24 (19): 2217–2227. Bibcode:2014CBio...24.2217H. doi:10.1016/j.cub.2014.08.006. PMC 4194317. PMID 25201686.

immunophenotyping.org (Global: low place; English: low place)

"Infection and Immunity Immunophenotyping (3i) Consortium".^{[permanent dead link]}

marrvel.org (Global: low place; English: low place)

"MARRVEL: Search Result". marrvel.org. Retrieved 2017-11-30.

mousephenotype.org (Global: low place; English: low place)

"International Mouse Phenotyping Consortium".

nih.gov (Global: 4^th place; English: 4^th place)

pubmed.ncbi.nlm.nih.gov

Castrop J, van Norren K, Clevers H (February 1992). "A gene family of HMG-box transcription factors with homology to TCF-1". Nucleic Acids Research. 20 (3): 611. doi:10.1093/nar/20.3.611. PMC 310434. PMID 1741298.
Jin T, Liu L (November 2008). "The Wnt signaling pathway effector TCF7L2 and type 2 diabetes mellitus". Molecular Endocrinology. 22 (11): 2383–2392. doi:10.1210/me.2008-0135. PMID 18599616.
Zhang C, Bao W, Rong Y, Yang H, Bowers K, Yeung E, et al. (2013-05-19). "Genetic variants and the risk of gestational diabetes mellitus: a systematic review". Human Reproduction Update. 19 (4): 376–390. doi:10.1093/humupd/dmt013. PMC 3682671. PMID 23690305.
Fitzgerald TW, Gerety SS, Jones WD, Van Kogelenberg M, King DA, McRae J, et al. (Deciphering Developmental Disorders Study) (March 2015). "Large-scale discovery of novel genetic causes of developmental disorders". Nature. 519 (7542): 223–228. Bibcode:2015Natur.519..223T. doi:10.1038/nature14135. PMC 5955210. PMID 25533962.
Clayton S, Fitzgerald TW, Kaplanis J, Prigmore E, Rajan D, Sifrim A, et al. (Deciphering Developmental Disorders Study) (February 2017). "Prevalence and architecture of de novo mutations in developmental disorders". Nature. 542 (7642): 433–438. Bibcode:2017Natur.542..433M. doi:10.1038/nature21062. PMC 6016744. PMID 28135719.
Hansen T, Ingason A, Djurovic S, Melle I, Fenger M, Gustafsson O, et al. (July 2011). "At-risk variant in TCF7L2 for type II diabetes increases risk of schizophrenia". Biological Psychiatry. 70 (1): 59–63. doi:10.1016/j.biopsych.2011.01.031. PMID 21414605. S2CID 42205809.
Liu L, Li J, Yan M, Li J, Chen J, Zhang Y, et al. (April 2017). "TCF7L2 polymorphisms and the risk of schizophrenia in the Chinese Han population". Oncotarget. 8 (17): 28614–28620. doi:10.18632/oncotarget.15603. PMC 5438676. PMID 28404897.
Wang T, Hoekzema K, Vecchio D, Wu H, Sulovari A, Coe BP, et al. (October 2020). "Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders". Nature Communications. 11 (1) 4932. Bibcode:2020NatCo..11.4932W. doi:10.1038/s41467-020-18723-y. PMC 7530681. PMID 33004838.
Satterstrom FK, Kosmicki JA, Wang J, Breen MS, De Rubeis S, An JY, et al. (February 2020). "Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism". Cell. 180 (3): 568–584.e23. doi:10.1016/j.cell.2019.12.036. PMC 7250485. PMID 31981491.
Torres S, García-Palmero I, Marín-Vicente C, Bartolomé RA, Calviño E, Fernández-Aceñero MJ, et al. (January 2018). "Proteomic Characterization of Transcription and Splicing Factors Associated with a Metastatic Phenotype in Colorectal Cancer". Journal of Proteome Research. 17 (1): 252–264. doi:10.1021/acs.jproteome.7b00548. hdl:10261/160082. PMID 29131639.
Vallée A, Vallée JN, Guillevin R, Lecarpentier Y (May 2018). "Interactions Between the Canonical WNT/Beta-Catenin Pathway and PPAR Gamma on Neuroinflammation, Demyelination, and Remyelination in Multiple Sclerosis". Cellular and Molecular Neurobiology. 38 (4): 783–795. doi:10.1007/s10571-017-0550-9. PMC 11482031. PMID 28905149. S2CID 4620853.
Vaquero AR, Ferreira NE, Omae SV, Rodrigues MV, Teixeira SK, Krieger JE, et al. (October 2012). "Using gene-network landscape to dissect genotype effects of TCF7L2 genetic variant on diabetes and cardiovascular risk". Physiological Genomics. 44 (19): 903–914. doi:10.1152/physiolgenomics.00030.2012. PMID 22872755. S2CID 35065699.
PDB: 2GL7; Sampietro J, Dahlberg CL, Cho US, Hinds TR, Kimelman D, Xu W (October 2006). "Crystal structure of a beta-catenin/BCL9/Tcf4 complex". Molecular Cell. 24 (2): 293–300. doi:10.1016/j.molcel.2006.09.001. PMID 17052462.
Lee JM, Dedhar S, Kalluri R, Thompson EW (March 2006). "The epithelial-mesenchymal transition: new insights in signaling, development, and disease". The Journal of Cell Biology. 172 (7): 973–981. doi:10.1083/jcb.200601018. PMC 2063755. PMID 16567498.
Facchinello N, Tarifeño-Saldivia E, Grisan E, Schiavone M, Peron M, Mongera A, et al. (August 2017). "Tcf7l2 plays pleiotropic roles in the control of glucose homeostasis, pancreas morphology, vascularization and regeneration". Scientific Reports. 7 (1) 9605. Bibcode:2017NatSR...7.9605F. doi:10.1038/s41598-017-09867-x. PMC 5575064. PMID 28851992.
Lipiec MA, Bem J, Koziński K, Chakraborty C, Urban-Ciećko J, Zajkowski T, et al. (August 2020). "TCF7L2 regulates postmitotic differentiation programmes and excitability patterns in the thalamus". Development. 147 (16) dev.190181. doi:10.1242/dev.190181 (inactive 13 November 2025). PMC 7473649. PMID 32675279.{{cite journal}}: CS1 maint: DOI inactive as of November 2025 (link)
Chen Y, Zhao Y, Li YB, Wang YJ, Zhang GZ (January 2018). "Detection of SNPs of T2DM susceptibility genes by a ligase detection reaction-fluorescent nanosphere technique". Analytical Biochemistry. 540–541 (Supplement C): 38–44. doi:10.1016/j.ab.2017.11.003. PMID 29128291.
Zhu L, Xie Z, Lu J, Hao Q, Kang M, Chen S, et al. (September 2017). "TCF7L2 rs290481 T>C polymorphism is associated with an increased risk of type 2 diabetes mellitus and fasting plasma glucose level". Oncotarget. 8 (44): 77000–77008. doi:10.18632/oncotarget.20300. PMC 5652758. PMID 29100364.
Nagalski A, Irimia M, Szewczyk L, Ferran JL, Misztal K, Kuznicki J, et al. (November 2013). "Postnatal isoform switch and protein localization of LEF1 and TCF7L2 transcription factors in cortical, thalamic, and mesencephalic regions of the adult mouse brain". Brain Structure & Function. 218 (6): 1531–1549. doi:10.1007/s00429-012-0474-6. PMC 3825142. PMID 23152144.
Murray KD, Rubin CM, Jones EG, Chalupa LM (November 2008). "Molecular correlates of laminar differences in the macaque dorsal lateral geniculate nucleus". The Journal of Neuroscience. 28 (46): 12010–12022. doi:10.1523/JNEUROSCI.3800-08.2008. PMC 2613947. PMID 19005066.
Nobrega MA (March 2013). "TCF7L2 and glucose metabolism: time to look beyond the pancreas". Diabetes. 62 (3): 706–708. doi:10.2337/db12-1418. PMC 3581232. PMID 23431017.
Duggirala R, Blangero J, Almasy L, Dyer TD, Williams KL, Leach RJ, et al. (April 1999). "Linkage of type 2 diabetes mellitus and of age at onset to a genetic location on chromosome 10q in Mexican Americans". American Journal of Human Genetics. 64 (4): 1127–1140. doi:10.1086/302316. PMC 1377837. PMID 10090898.
Grant SF, Thorleifsson G, Reynisdottir I, Benediktsson R, Manolescu A, Sainz J, et al. (March 2006). "Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes". Nature Genetics. 38 (3): 320–323. doi:10.1038/ng1732. PMID 16415884. S2CID 28825825.
Jin T (June 2016). "Current Understanding on Role of the Wnt Signaling Pathway Effector TCF7L2 in Glucose Homeostasis". Endocrine Reviews. 37 (3): 254–277. doi:10.1210/er.2015-1146. PMID 27159876.
Slattery ML, Folsom AR, Wolff R, Herrick J, Caan BJ, Potter JD (April 2008). "Transcription factor 7-like 2 polymorphism and colon cancer". Cancer Epidemiology, Biomarkers & Prevention. 17 (4): 978–982. doi:10.1158/1055-9965.EPI-07-2687. PMC 2587179. PMID 18398040.
Hazra A, Fuchs CS, Chan AT, Giovannucci EL, Hunter DJ (November 2008). "Association of the TCF7L2 polymorphism with colorectal cancer and adenoma risk". Cancer Causes & Control. 19 (9): 975–980. doi:10.1007/s10552-008-9164-3. PMC 2719293. PMID 18478343.
Tang W, Dodge M, Gundapaneni D, Michnoff C, Roth M, Lum L (July 2008). "A genome-wide RNAi screen for Wnt/beta-catenin pathway components identifies unexpected roles for TCF transcription factors in cancer". Proceedings of the National Academy of Sciences of the United States of America. 105 (28): 9697–9702. Bibcode:2008PNAS..105.9697T. doi:10.1073/pnas.0804709105. PMC 2453074. PMID 18621708.
Sun P, Xiong H, Kim TH, Ren B, Zhang Z (February 2006). "Positive inter-regulation between beta-catenin/T cell factor-4 signaling and endothelin-1 signaling potentiates proliferation and survival of prostate cancer cells". Molecular Pharmacology. 69 (2): 520–531. doi:10.1124/mol.105.019620. PMID 16291872. S2CID 10148857.
Beretta CA, Dross N, Bankhead P, Carl M (September 2013). "The ventral habenulae of zebrafish develop in prosomere 2 dependent on Tcf7l2 function". Neural Development. 8 (1) 19. doi:10.1186/1749-8104-8-19. PMC 3827927. PMID 24067090.
Hüsken U, Stickney HL, Gestri G, Bianco IH, Faro A, Young RM, et al. (October 2014). "Tcf7l2 is required for left-right asymmetric differentiation of habenular neurons". Current Biology. 24 (19): 2217–2227. Bibcode:2014CBio...24.2217H. doi:10.1016/j.cub.2014.08.006. PMC 4194317. PMID 25201686.
Vacik T, Stubbs JL, Lemke G (September 2011). "A novel mechanism for the transcriptional regulation of Wnt signaling in development". Genes & Development. 25 (17): 1783–1795. doi:10.1101/gad.17227011. PMC 3175715. PMID 21856776.
Chodelkova O, Masek J, Korinek V, Kozmik Z, Machon O (May 2018). "Tcf7L2 is essential for neurogenesis in the developing mouse neocortex". Neural Development. 13 (1) 8. doi:10.1186/s13064-018-0107-8. PMC 5946422. PMID 29751817.
Lee M, Yoon J, Song H, Lee B, Lam DT, Yoon J, et al. (April 2017). "Tcf7l2 plays crucial roles in forebrain development through regulation of thalamic and habenular neuron identity and connectivity". Developmental Biology. 424 (1): 62–76. doi:10.1016/j.ydbio.2017.02.010. PMID 28219675.
de Zwarte SM, Brouwer RM, Tsouli A, Cahn W, Hillegers MH, Hulshoff Pol HE, et al. (October 2019). "Running in the Family? Structural Brain Abnormalities and IQ in Offspring, Siblings, Parents, and Co-twins of Patients with Schizophrenia". Schizophrenia Bulletin. 45 (6): 1209–1217. doi:10.1093/schbul/sby182. PMC 6811835. PMID 30597053.
Giraldo-Chica M, Woodward ND (February 2017). "Review of thalamocortical resting-state fMRI studies in schizophrenia". Schizophrenia Research. Pathologies of the Thalamus in Schizophrenia. 180: 58–63. doi:10.1016/j.schres.2016.08.005. PMC 5297399. PMID 27531067.
Hua J, Blair NI, Paez A, Choe A, Barber AD, Brandt A, et al. (April 2019). "Altered functional connectivity between sub-regions in the thalamus and cortex in schizophrenia patients measured by resting state BOLD fMRI at 7T". Schizophrenia Research. 206: 370–377. doi:10.1016/j.schres.2018.10.016. PMC 6500777. PMID 30409697.
van Erp TG, Walton E, Hibar DP, Schmaal L, Jiang W, Glahn DC, et al. (November 2018). "Cortical Brain Abnormalities in 4474 Individuals With Schizophrenia and 5098 Control Subjects via the Enhancing Neuro Imaging Genetics Through Meta Analysis (ENIGMA) Consortium". Biological Psychiatry. 84 (9): 644–654. doi:10.1016/j.biopsych.2018.04.023. PMC 6177304. PMID 29960671.
Ayub R, Sun KL, Flores RE, Lam VT, Jo B, Saggar M, et al. (February 2021). "Thalamocortical connectivity is associated with autism symptoms in high-functioning adults with autism and typically developing adults". Translational Psychiatry. 11 (1) 93. doi:10.1038/s41398-021-01221-0. PMC 7859407. PMID 33536431.
Schuetze M, Park MT, Cho IY, MacMaster FP, Chakravarty MM, Bray SL (October 2016). "Morphological Alterations in the Thalamus, Striatum, and Pallidum in Autism Spectrum Disorder". Neuropsychopharmacology. 41 (11): 2627–2637. doi:10.1038/npp.2016.64. PMC 5026732. PMID 27125303.
Tomasi D, Volkow ND (February 2019). "Reduced Local and Increased Long-Range Functional Connectivity of the Thalamus in Autism Spectrum Disorder". Cerebral Cortex. 29 (2): 573–585. doi:10.1093/cercor/bhx340. PMC 6319176. PMID 29300843.
Woodward ND, Giraldo-Chica M, Rogers B, Cascio CJ (January 2017). "Thalamocortical dysconnectivity in autism spectrum disorder: An analysis of the Autism Brain Imaging Data Exchange". Biological Psychiatry. Cognitive Neuroscience and Neuroimaging. 2 (1): 76–84. doi:10.1016/j.bpsc.2016.09.002. PMC 5455796. PMID 28584881.
Skarnes WC, Rosen B, West AP, Koutsourakis M, Bushell W, Iyer V, et al. (June 2011). "A conditional knockout resource for the genome-wide study of mouse gene function". Nature. 474 (7351): 337–342. doi:10.1038/nature10163. PMC 3572410. PMID 21677750.
Dolgin E (June 2011). "Mouse library set to be knockout". Nature. 474 (7351): 262–263. doi:10.1038/474262a. PMID 21677718.
Collins FS, Rossant J, Wurst W (January 2007). "A mouse for all reasons". Cell. 128 (1): 9–13. doi:10.1016/j.cell.2006.12.018. PMID 17218247. S2CID 18872015.
White JK, Gerdin AK, Karp NA, Ryder E, Buljan M, Bussell JN, et al. (July 2013). "Genome-wide generation and systematic phenotyping of knockout mice reveals new roles for many genes". Cell. 154 (2): 452–464. doi:10.1016/j.cell.2013.06.022. PMC 3717207. PMID 23870131.

ncbi.nlm.nih.gov

"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Entrez Gene: TCF7L2".
Castrop J, van Norren K, Clevers H (February 1992). "A gene family of HMG-box transcription factors with homology to TCF-1". Nucleic Acids Research. 20 (3): 611. doi:10.1093/nar/20.3.611. PMC 310434. PMID 1741298.
"TCF7L2 transcription factor 7 like 2 [Homo sapiens (human)] - Gene - NCBI". www.ncbi.nlm.nih.gov. Retrieved 2017-11-30.
Zhang C, Bao W, Rong Y, Yang H, Bowers K, Yeung E, et al. (2013-05-19). "Genetic variants and the risk of gestational diabetes mellitus: a systematic review". Human Reproduction Update. 19 (4): 376–390. doi:10.1093/humupd/dmt013. PMC 3682671. PMID 23690305.
Fitzgerald TW, Gerety SS, Jones WD, Van Kogelenberg M, King DA, McRae J, et al. (Deciphering Developmental Disorders Study) (March 2015). "Large-scale discovery of novel genetic causes of developmental disorders". Nature. 519 (7542): 223–228. Bibcode:2015Natur.519..223T. doi:10.1038/nature14135. PMC 5955210. PMID 25533962.
Clayton S, Fitzgerald TW, Kaplanis J, Prigmore E, Rajan D, Sifrim A, et al. (Deciphering Developmental Disorders Study) (February 2017). "Prevalence and architecture of de novo mutations in developmental disorders". Nature. 542 (7642): 433–438. Bibcode:2017Natur.542..433M. doi:10.1038/nature21062. PMC 6016744. PMID 28135719.
Liu L, Li J, Yan M, Li J, Chen J, Zhang Y, et al. (April 2017). "TCF7L2 polymorphisms and the risk of schizophrenia in the Chinese Han population". Oncotarget. 8 (17): 28614–28620. doi:10.18632/oncotarget.15603. PMC 5438676. PMID 28404897.
Wang T, Hoekzema K, Vecchio D, Wu H, Sulovari A, Coe BP, et al. (October 2020). "Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders". Nature Communications. 11 (1) 4932. Bibcode:2020NatCo..11.4932W. doi:10.1038/s41467-020-18723-y. PMC 7530681. PMID 33004838.
Satterstrom FK, Kosmicki JA, Wang J, Breen MS, De Rubeis S, An JY, et al. (February 2020). "Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism". Cell. 180 (3): 568–584.e23. doi:10.1016/j.cell.2019.12.036. PMC 7250485. PMID 31981491.
Vallée A, Vallée JN, Guillevin R, Lecarpentier Y (May 2018). "Interactions Between the Canonical WNT/Beta-Catenin Pathway and PPAR Gamma on Neuroinflammation, Demyelination, and Remyelination in Multiple Sclerosis". Cellular and Molecular Neurobiology. 38 (4): 783–795. doi:10.1007/s10571-017-0550-9. PMC 11482031. PMID 28905149. S2CID 4620853.
Lee JM, Dedhar S, Kalluri R, Thompson EW (March 2006). "The epithelial-mesenchymal transition: new insights in signaling, development, and disease". The Journal of Cell Biology. 172 (7): 973–981. doi:10.1083/jcb.200601018. PMC 2063755. PMID 16567498.
Facchinello N, Tarifeño-Saldivia E, Grisan E, Schiavone M, Peron M, Mongera A, et al. (August 2017). "Tcf7l2 plays pleiotropic roles in the control of glucose homeostasis, pancreas morphology, vascularization and regeneration". Scientific Reports. 7 (1) 9605. Bibcode:2017NatSR...7.9605F. doi:10.1038/s41598-017-09867-x. PMC 5575064. PMID 28851992.
Lipiec MA, Bem J, Koziński K, Chakraborty C, Urban-Ciećko J, Zajkowski T, et al. (August 2020). "TCF7L2 regulates postmitotic differentiation programmes and excitability patterns in the thalamus". Development. 147 (16) dev.190181. doi:10.1242/dev.190181 (inactive 13 November 2025). PMC 7473649. PMID 32675279.{{cite journal}}: CS1 maint: DOI inactive as of November 2025 (link)
Zhu L, Xie Z, Lu J, Hao Q, Kang M, Chen S, et al. (September 2017). "TCF7L2 rs290481 T>C polymorphism is associated with an increased risk of type 2 diabetes mellitus and fasting plasma glucose level". Oncotarget. 8 (44): 77000–77008. doi:10.18632/oncotarget.20300. PMC 5652758. PMID 29100364.
Nagalski A, Irimia M, Szewczyk L, Ferran JL, Misztal K, Kuznicki J, et al. (November 2013). "Postnatal isoform switch and protein localization of LEF1 and TCF7L2 transcription factors in cortical, thalamic, and mesencephalic regions of the adult mouse brain". Brain Structure & Function. 218 (6): 1531–1549. doi:10.1007/s00429-012-0474-6. PMC 3825142. PMID 23152144.
Murray KD, Rubin CM, Jones EG, Chalupa LM (November 2008). "Molecular correlates of laminar differences in the macaque dorsal lateral geniculate nucleus". The Journal of Neuroscience. 28 (46): 12010–12022. doi:10.1523/JNEUROSCI.3800-08.2008. PMC 2613947. PMID 19005066.
Nobrega MA (March 2013). "TCF7L2 and glucose metabolism: time to look beyond the pancreas". Diabetes. 62 (3): 706–708. doi:10.2337/db12-1418. PMC 3581232. PMID 23431017.
Duggirala R, Blangero J, Almasy L, Dyer TD, Williams KL, Leach RJ, et al. (April 1999). "Linkage of type 2 diabetes mellitus and of age at onset to a genetic location on chromosome 10q in Mexican Americans". American Journal of Human Genetics. 64 (4): 1127–1140. doi:10.1086/302316. PMC 1377837. PMID 10090898.
Slattery ML, Folsom AR, Wolff R, Herrick J, Caan BJ, Potter JD (April 2008). "Transcription factor 7-like 2 polymorphism and colon cancer". Cancer Epidemiology, Biomarkers & Prevention. 17 (4): 978–982. doi:10.1158/1055-9965.EPI-07-2687. PMC 2587179. PMID 18398040.
Hazra A, Fuchs CS, Chan AT, Giovannucci EL, Hunter DJ (November 2008). "Association of the TCF7L2 polymorphism with colorectal cancer and adenoma risk". Cancer Causes & Control. 19 (9): 975–980. doi:10.1007/s10552-008-9164-3. PMC 2719293. PMID 18478343.
Tang W, Dodge M, Gundapaneni D, Michnoff C, Roth M, Lum L (July 2008). "A genome-wide RNAi screen for Wnt/beta-catenin pathway components identifies unexpected roles for TCF transcription factors in cancer". Proceedings of the National Academy of Sciences of the United States of America. 105 (28): 9697–9702. Bibcode:2008PNAS..105.9697T. doi:10.1073/pnas.0804709105. PMC 2453074. PMID 18621708.
Beretta CA, Dross N, Bankhead P, Carl M (September 2013). "The ventral habenulae of zebrafish develop in prosomere 2 dependent on Tcf7l2 function". Neural Development. 8 (1) 19. doi:10.1186/1749-8104-8-19. PMC 3827927. PMID 24067090.
Hüsken U, Stickney HL, Gestri G, Bianco IH, Faro A, Young RM, et al. (October 2014). "Tcf7l2 is required for left-right asymmetric differentiation of habenular neurons". Current Biology. 24 (19): 2217–2227. Bibcode:2014CBio...24.2217H. doi:10.1016/j.cub.2014.08.006. PMC 4194317. PMID 25201686.
Vacik T, Stubbs JL, Lemke G (September 2011). "A novel mechanism for the transcriptional regulation of Wnt signaling in development". Genes & Development. 25 (17): 1783–1795. doi:10.1101/gad.17227011. PMC 3175715. PMID 21856776.
Chodelkova O, Masek J, Korinek V, Kozmik Z, Machon O (May 2018). "Tcf7L2 is essential for neurogenesis in the developing mouse neocortex". Neural Development. 13 (1) 8. doi:10.1186/s13064-018-0107-8. PMC 5946422. PMID 29751817.
de Zwarte SM, Brouwer RM, Tsouli A, Cahn W, Hillegers MH, Hulshoff Pol HE, et al. (October 2019). "Running in the Family? Structural Brain Abnormalities and IQ in Offspring, Siblings, Parents, and Co-twins of Patients with Schizophrenia". Schizophrenia Bulletin. 45 (6): 1209–1217. doi:10.1093/schbul/sby182. PMC 6811835. PMID 30597053.
Giraldo-Chica M, Woodward ND (February 2017). "Review of thalamocortical resting-state fMRI studies in schizophrenia". Schizophrenia Research. Pathologies of the Thalamus in Schizophrenia. 180: 58–63. doi:10.1016/j.schres.2016.08.005. PMC 5297399. PMID 27531067.
Hua J, Blair NI, Paez A, Choe A, Barber AD, Brandt A, et al. (April 2019). "Altered functional connectivity between sub-regions in the thalamus and cortex in schizophrenia patients measured by resting state BOLD fMRI at 7T". Schizophrenia Research. 206: 370–377. doi:10.1016/j.schres.2018.10.016. PMC 6500777. PMID 30409697.
van Erp TG, Walton E, Hibar DP, Schmaal L, Jiang W, Glahn DC, et al. (November 2018). "Cortical Brain Abnormalities in 4474 Individuals With Schizophrenia and 5098 Control Subjects via the Enhancing Neuro Imaging Genetics Through Meta Analysis (ENIGMA) Consortium". Biological Psychiatry. 84 (9): 644–654. doi:10.1016/j.biopsych.2018.04.023. PMC 6177304. PMID 29960671.
Ayub R, Sun KL, Flores RE, Lam VT, Jo B, Saggar M, et al. (February 2021). "Thalamocortical connectivity is associated with autism symptoms in high-functioning adults with autism and typically developing adults". Translational Psychiatry. 11 (1) 93. doi:10.1038/s41398-021-01221-0. PMC 7859407. PMID 33536431.
Schuetze M, Park MT, Cho IY, MacMaster FP, Chakravarty MM, Bray SL (October 2016). "Morphological Alterations in the Thalamus, Striatum, and Pallidum in Autism Spectrum Disorder". Neuropsychopharmacology. 41 (11): 2627–2637. doi:10.1038/npp.2016.64. PMC 5026732. PMID 27125303.
Tomasi D, Volkow ND (February 2019). "Reduced Local and Increased Long-Range Functional Connectivity of the Thalamus in Autism Spectrum Disorder". Cerebral Cortex. 29 (2): 573–585. doi:10.1093/cercor/bhx340. PMC 6319176. PMID 29300843.
Woodward ND, Giraldo-Chica M, Rogers B, Cascio CJ (January 2017). "Thalamocortical dysconnectivity in autism spectrum disorder: An analysis of the Autism Brain Imaging Data Exchange". Biological Psychiatry. Cognitive Neuroscience and Neuroimaging. 2 (1): 76–84. doi:10.1016/j.bpsc.2016.09.002. PMC 5455796. PMID 28584881.
Skarnes WC, Rosen B, West AP, Koutsourakis M, Bushell W, Iyer V, et al. (June 2011). "A conditional knockout resource for the genome-wide study of mouse gene function". Nature. 474 (7351): 337–342. doi:10.1038/nature10163. PMC 3572410. PMID 21677750.
White JK, Gerdin AK, Karp NA, Ryder E, Buljan M, Bussell JN, et al. (July 2013). "Genome-wide generation and systematic phenotyping of knockout mice reveals new roles for many genes". Cell. 154 (2): 452–464. doi:10.1016/j.cell.2013.06.022. PMC 3717207. PMID 23870131.

omim.org (Global: 4,380^th place; English: 4,305^th place)

Online Mendelian Inheritance in Man (OMIM): TRANSCRIPTION FACTOR 7-LIKE 2;TCF7L2 - 602228{

rcsb.org (Global: 8,838^th place; English: 8,783^rd place)

PDB: 2GL7; Sampietro J, Dahlberg CL, Cho US, Hinds TR, Kimelman D, Xu W (October 2006). "Crystal structure of a beta-catenin/BCL9/Tcf4 complex". Molecular Cell. 24 (2): 293–300. doi:10.1016/j.molcel.2006.09.001. PMID 17052462.

semanticscholar.org (Global: 11^th place; English: 8^th place)

api.semanticscholar.org

Hansen T, Ingason A, Djurovic S, Melle I, Fenger M, Gustafsson O, et al. (July 2011). "At-risk variant in TCF7L2 for type II diabetes increases risk of schizophrenia". Biological Psychiatry. 70 (1): 59–63. doi:10.1016/j.biopsych.2011.01.031. PMID 21414605. S2CID 42205809.
Vallée A, Vallée JN, Guillevin R, Lecarpentier Y (May 2018). "Interactions Between the Canonical WNT/Beta-Catenin Pathway and PPAR Gamma on Neuroinflammation, Demyelination, and Remyelination in Multiple Sclerosis". Cellular and Molecular Neurobiology. 38 (4): 783–795. doi:10.1007/s10571-017-0550-9. PMC 11482031. PMID 28905149. S2CID 4620853.
Vaquero AR, Ferreira NE, Omae SV, Rodrigues MV, Teixeira SK, Krieger JE, et al. (October 2012). "Using gene-network landscape to dissect genotype effects of TCF7L2 genetic variant on diabetes and cardiovascular risk". Physiological Genomics. 44 (19): 903–914. doi:10.1152/physiolgenomics.00030.2012. PMID 22872755. S2CID 35065699.
Grant SF, Thorleifsson G, Reynisdottir I, Benediktsson R, Manolescu A, Sainz J, et al. (March 2006). "Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes". Nature Genetics. 38 (3): 320–323. doi:10.1038/ng1732. PMID 16415884. S2CID 28825825.
Sun P, Xiong H, Kim TH, Ren B, Zhang Z (February 2006). "Positive inter-regulation between beta-catenin/T cell factor-4 signaling and endothelin-1 signaling potentiates proliferation and survival of prostate cancer cells". Molecular Pharmacology. 69 (2): 520–531. doi:10.1124/mol.105.019620. PMID 16291872. S2CID 10148857.
Gerdin AK (2010). "The Sanger Mouse Genetics Programme: high throughput characterisation of knockout mice". Acta Ophthalmologica. 88: 925–7. doi:10.1111/j.1755-3768.2010.4142.x. S2CID 85911512.
Collins FS, Rossant J, Wurst W (January 2007). "A mouse for all reasons". Cell. 128 (1): 9–13. doi:10.1016/j.cell.2006.12.018. PMID 17218247. S2CID 18872015.

sfari.org (Global: low place; English: low place)

gene.sfari.org

"SFARI Gene Database - TCF7L2". Retrieved 2022-07-16.

uniprot.org (Global: 5,673^rd place; English: 6,418^th place)

"TCF7L2 - Transcription factor 7-like 2 - Homo sapiens (Human) - TCF7L2 gene & protein". www.uniprot.org. Retrieved 2017-11-30.

TCF7L2 (English Wikipedia)

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