References analysis of the Wikipedia article "RCCX" in the Galician version

doi.org (Global: 2^nd place; Galician: 7^th place)

dx.doi.org

Chang SF, Lee HH (2011). "Analysis of the CYP21A2 gene with intergenic recombination and multiple gene deletions in the RCCX module". Genet Test Mol Biomarkers 15 (1–2): 35–42. PMID 21117955. doi:10.1089/gtmb.2010.0080.

Bánlaki Z, Doleschall M, Rajczy K, Fust G, Szilágyi A (outubro de 2012). "Fine-tuned characterization of RCCX copy number variants and their relationship with extended MHC haplotypes". Genes Immun 13 (7): 530–535. PMID 22785613. doi:10.1038/gene.2012.29.

Carrozza C, Foca L, De Paolis E, Concolino P (2021). "Genes and Pseudogenes: Complexity of the RCCX Locus and Disease". Front Endocrinol (Lausanne) 12. 709758. PMC 8362596. PMID 34394006. doi:10.3389/fendo.2021.709758.

Sweeten TL, Odell DW, Odell JD, Torres AR (xaneiro de 2008). "C4B null alleles are not associated with genetic polymorphisms in the adjacent gene CYP21A2 in autism". BMC Medical Genetics 9: 1. PMC 2265260. PMID 18179706. doi:10.1186/1471-2350-9-1.

Dangel AW, Mendoza AR, Baker BJ, Daniel CM, Carroll MC, Wu LC, Yu CY (1994). "The dichotomous size variation of human complement C4 genes is mediated by a novel family of endogenous retroviruses, which also establishes species-specific genomic patterns among Old World primates". Immunogenetics 40 (6): 425–436. PMID 7545960. doi:10.1007/BF00177825.

Kim JH, Kim GH, Yoo HW, Choi JH (xuño de 2023). "Molecular basis and genetic testing strategies for diagnosing 21-hydroxylase deficiency, including CAH-X syndrome". Ann Pediatr Endocrinol Metab 28 (2): 77–86. PMC 10329939. PMID 37401054. doi:10.6065/apem.2346108.054.

Bánlaki Z, Szabó JA, Szilágyi Á, Patócs A, Prohászka Z, Füst G, Doleschall M (2013). "Intraspecific evolution of human RCCX copy number variation traced by haplotypes of the CYP21A2 gene". Genome Biol Evol 5 (1): 98–112. PMC 3595039. PMID 23241443. doi:10.1093/gbe/evs121.

Tsai LP, Lee HH (setembro de 2012). "Analysis of CYP21A1P and the duplicated CYP21A2 genes". Gene 506 (1): 261–262. PMID 22771554. doi:10.1016/j.gene.2012.06.045.

Doleschall M, Luczay A, Koncz K, Hadzsiev K, Erhardt É, Szilágyi Á, Doleschall Z, Németh K, Török D, Prohászka Z, Gereben B, Fekete G, Gláz E, Igaz P, Korbonits M, Tóth M, Rácz K, Patócs A (xuño de 2017). "A unique haplotype of RCCX copy number variation: from the clinics of congenital adrenal hyperplasia to evolutionary genetics". Eur J Hum Genet 25 (6): 702–710. PMC 5477366. PMID 28401898. doi:10.1038/ejhg.2017.38.

Zhou D, Rudnicki M, Chua GT, Lawrance SK, Zhou B, Drew JL, Barbar-Smiley F, Armstrong TK, Hilt ME, Birmingham DJ, Passler W, Auletta JJ, Bowden SA, Hoffman RP, Wu YL, Jarjour WN, Mok CC, Ardoin SP, Lau YL, Yu CY (2021). "Human Complement C4B Allotypes and Deficiencies in Selected Cases With Autoimmune Diseases". Front Immunol 12. 739430. PMC 8577214. PMID 34764957. doi:10.3389/fimmu.2021.739430.

Milner CM, Campbell RD (agosto de 2001). "Genetic organization of the human MHC class III region". Frontiers in Bioscience: A Journal and Virtual Library 6: D914–26. PMID 11487476. doi:10.2741/milner.

Yu CY (1998). "Molecular genetics of the human MHC complement gene cluster". Exp Clin Immunogenet 15 (4): 213–230. PMID 10072631. doi:10.1159/000019075.

Yu CY, Chung EK, Yang Y, Blanchong CA, Jacobsen N, Saxena K, Yang Z, Miller W, Varga L, Fust G (2003). "Dancing with Complement C4 and the RP-C4-CYP21-TNX (RCCX) Modules of the Major Histocompatibility Complex". Prog Nucleic Acid Res Mol Biol. Progress in Nucleic Acid Research and Molecular Biology 75: 217–292. ISBN 9780125400756. PMID 14604014. doi:10.1016/s0079-6603(03)75007-7.

Xie T, Rowen L, Aguado B, Ahearn ME, Madan A, Qin S, Campbell RD, Hood L (decembro de 2003). "Analysis of the gene-dense major histocompatibility complex class III region and its comparison to mouse". Genome Research 13 (12): 2621–36. PMC 403804. PMID 14656967. doi:10.1101/gr.1736803.

Rupert KL, Rennebohm RM, Yu CY (1999). "An unequal crossover between the RCCX modules of the human MHC leading to the presence of a CYP21B gene and a tenascin TNXB/TNXA-RP2 recombinant between C4A and C4B genes in a patient with juvenile rheumatoid arthritis". Exp Clin Immunogenet 16 (2): 81–97. PMID 10343159. doi:10.1159/000019099.

Espinosa Reyes TM, Collazo Mesa T, Lantigua Cruz PA, Agramonte Machado A, Domínguez Alonso E, Falhammar H (novembro de 2020). "Molecular diagnosis of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency". BMC Endocrine Disorders 20 (1): 165. PMC 7653887. PMID 33168061. doi:10.1186/s12902-020-00643-z.

Lee HH (xaneiro de 2005). "Chimeric CYP21P/CYP21 and TNXA/TNXB genes in the RCCX module". Mol Genet Metab 84 (1): 4–8. PMID 15639189. doi:10.1016/j.ymgme.2004.09.009.

Asquith CRM, Temme L (setembro de 2020). "STK19: a new target for NRAS-driven cancer". Nat Rev Drug Discov 19 (9): 579. PMID 32587355. doi:10.1038/d41573-020-00116-x.

Yin C, Zhu B, Zhang T, Liu T, Chen S, Liu Y, Li X, Miao X, Li S, Mi X, Zhang J, Li L, Wei G, Xu ZX, Gao X, Huang C, Wei Z, Goding CR, Wang P, Deng X, Cui R (febreiro de 2019). "Pharmacological Targeting of STK19 Inhibits Oncogenic NRAS-Driven Melanomagenesis". Cell 176 (5): 1113–1127.e16. PMID 30712867. doi:10.1016/j.cell.2019.01.002. Arquivado dende o orixinal o 8 de marzo de 2024. Consultado o 8 de marzo de 2024.

Rodríguez-Martínez M, Boissiére T, Noe Gonzalez M, Litchfield K, Mitter R, Walker J, Kjœr S, Ismail M, Downward J, Swanton C, Svejstrup JQ (xuño de 2020). "Evidence That STK19 Is Not an NRAS-dependent Melanoma Driver". Cell 181 (6): 1395–1405.e11. PMC 7298618. PMID 32531245. doi:10.1016/j.cell.2020.04.014.

Yin C, Zhu B, Li X, Goding CR, Cui R (xuño de 2020). "A Reply to "Evidence that STK19 Is Not an NRAS-Dependent Melanoma Driver"". Cell 181 (6): 1406–1409.e2. PMID 32531246. doi:10.1016/j.cell.2020.04.029.

Pereira KM, Faria AG, Liphaus BL, Jesus AA, Silva CA, Carneiro-Sampaio M, Andrade LE (maio de 2016). "Low C4, C4A and C4B gene copy numbers are stronger risk factors for juvenile-onset than for adult-onset systemic lupus erythematosus". Rheumatology (Oxford) 55 (5): 869–73. PMID 26800705. doi:10.1093/rheumatology/kev436.

Marino R, Moresco A, Perez Garrido N, Ramirez P, Belgorosky A (2022). "Congenital Adrenal Hyperplasia and Ehlers-Danlos Syndrome". Front Endocrinol (Lausanne) 13: 803226. PMC 8913572. PMID 35282436. doi:10.3389/fendo.2022.803226.

Morissette R, Chen W, Perritt AF, Dreiling JL, Arai AE, Sachdev V, Hannoush H, Mallappa A, Xu Z, McDonnell NB, Quezado M, Merke DP (agosto de 2015). "Broadening the Spectrum of Ehlers Danlos Syndrome in Patients With Congenital Adrenal Hyperplasia". J Clin Endocrinol Metab 100 (8): E1143–52. PMC 4525000. PMID 26075496. doi:10.1210/jc.2015-2232.

Piero Portincasa; Gema Frühbeck; Hendrik M. Nathoe, eds. (2019). "Endocrine Disorders and Psychiatric Manifestations". Endocrinology and Systemic Diseases. Springer Cham. pp. 1–35. ISBN 978-3-319-66362-3. doi:10.1007/978-3-319-66362-3_12-1.

Wu Z, Zhang S, Li P, Zhang F, Li Y (novembro de 2020). "Association between complement 4 copy number variation and systemic lupus erythematosus: a meta-analysis". Clin Exp Med 20 (4): 627–634. PMID 32691186. doi:10.1007/s10238-020-00640-5.

Pereira KMC, Perazzio S, Faria AGA, Moreira ES, Santos VC, Grecco M, da Silva NP, Andrade LEC (agosto de 2019). "Impact of C4, C4A and C4B gene copy number variation in the susceptibility, phenotype and progression of systemic lupus erythematosus". Adv Rheumatol 59 (1): 36. PMID 31387635. doi:10.1186/s42358-019-0076-6.

Mason MJ, Speake C, Gersuk VH, Nguyen QA, O'Brien KK, Odegard JM, Buckner JH, Greenbaum CJ, Chaussabel D, Nepom GT (maio de 2014). "Low HERV-K(C4) copy number is associated with type 1 diabetes". Diabetes 63 (5): 1789–95. PMID 24430436. doi:10.2337/db13-1382.

Tsang-A-Sjoe MWP, Bultink IEM, Korswagen LA, van der Horst A, Rensink I, de Boer M, Hamann D, Voskuyl AE, Wouters D (decembro de 2017). "Comprehensive approach to study complement C4 in systemic lupus erythematosus: Gene polymorphisms, protein levels and functional activity". Mol Immunol 92: 125–131. PMID 29080553. doi:10.1016/j.molimm.2017.10.004.

Mack M, Bender K, Schneider PM (agosto de 2004). "Detection of retroviral antisense transcripts and promoter activity of the HERV-K(C4) insertion in the MHC class III region". Immunogenetics 56 (5): 321–332. PMID 15309346. doi:10.1007/s00251-004-0705-y.

Trowsdale J, Knight JC (2013). "Major histocompatibility complex genomics and human disease". Annu Rev Genomics Hum Genet 14: 301–323. PMC 4426292. PMID 23875801. doi:10.1146/annurev-genom-091212-153455.

Fanis P, Skordis N, Phylactou LA, Neocleous V (marzo de 2023). "Salt-wasting congenital adrenal hyperplasia phenotype as a result of the TNXA/TNXB chimera 1 (CAH-X CH-1) and the pathogenic IVS2-13A/C > G in CYP21A2 gene". Hormones (Athens) 22 (1): 71–77. PMC 10011304. PMID 36264454. doi:10.1007/s42000-022-00410-w.

Fanis P, Skordis N, Toumba M, Picolos M, Tanteles GA, Neocleous V, Phylactou LA (2023). "The pathogenic p.Gln319Ter variant is not causing congenital adrenal hyperplasia when inherited in one of the duplicated CYP21A2 genes". Front Endocrinol (Lausanne) 14. 1156616. PMC 10266209. PMID 37324257. doi:10.3389/fendo.2023.1156616.

Lao Q, Burkardt DD, Kollender S, Faucz FR, Merke DP (xullo de 2023). "Congenital adrenal hyperplasia due to two rare CYP21A2 variant alleles, including a novel attenuated CYP21A1P/CYP21A2 chimera". Mol Genet Genomic Med 11 (7). e2195. PMC 10337281. PMID 37157918. doi:10.1002/mgg3.2195.

Paragliola RM, Perrucci A, Foca L, Urbani A, Concolino P (xullo de 2022). "Prevalence of CAH-X Syndrome in Italian Patients with Congenital Adrenal Hyperplasia (CAH) Due to 21-Hydroxylase Deficiency". J Clin Med 11 (13): 3818. PMC 9267771. PMID 35807105. doi:10.3390/jcm11133818.

Ener RA, Meglathery SB, Van Decker WA, Gallagher RM (marzo de 2003). "Serotonin syndrome and other serotonergic disorders". Pain Med 4 (1): 63–74. PMID 12873279. doi:10.1046/j.1526-4637.2003.03005.x.

Ener RA, Meglathery SB, Styler M (xuño de 2004). "Extravasation of systemic hemato-oncological therapies". Ann Oncol 15 (6): 858–62. PMID 15151940. doi:10.1093/annonc/mdh214.

Ener RA, Meglathery SB, Cuhaci B, Topolsky D, Styler MJ, Crilley P, Brodsky I, Kahn SB, King RS (febreiro de 2001). "Use of granulocyte colony-stimulating factor after high-dose chemotherapy and autologous peripheral blood stem cell transplantation: what is the optimal timing?". Am J Clin Oncol 24 (1): 19–25. PMID 11232944. doi:10.1097/00000421-200102000-00003.

nih.gov (Global: 4^th place; Galician: 6^th place)

ncbi.nlm.nih.gov

Tsai LP, Lee HH (setembro de 2012). "Analysis of CYP21A1P and the duplicated CYP21A2 genes". Gene 506 (1): 261–262. PMID 22771554. doi:10.1016/j.gene.2012.06.045.

Yu CY (1998). "Molecular genetics of the human MHC complement gene cluster". Exp Clin Immunogenet 15 (4): 213–230. PMID 10072631. doi:10.1159/000019075.

Lee HH (xaneiro de 2005). "Chimeric CYP21P/CYP21 and TNXA/TNXB genes in the RCCX module". Mol Genet Metab 84 (1): 4–8. PMID 15639189. doi:10.1016/j.ymgme.2004.09.009.

Asquith CRM, Temme L (setembro de 2020). "STK19: a new target for NRAS-driven cancer". Nat Rev Drug Discov 19 (9): 579. PMID 32587355. doi:10.1038/d41573-020-00116-x.

Nimkarn S, Gangishetti PK, Yau M, New MI (4 de febreiro de 2016). Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJ, Gripp KW, Amemiya A, eds. "21-Hydroxylase-Deficient Congenital Adrenal Hyperplasia" (PDF). GeneReviews. PMID 20301350. NBK1171. Arquivado dende o orixinal (PDF) o 6 de novembro de 2022. Consultado o 8 de marzo de 2024.

NCBI RefSeq TNXA tenascin XA (pseudogene) [ Homo sapiens (human) ]

NCBI RefSeq TNXB tenascin XB [ Homo sapiens (human) ]

Denicoff KD, Meglathery SB, Post RM, Tandeciarz SI (febreiro de 1994). "Efficacy of carbamazepine compared with other agents: a clinical practice survey". J Clin Psychiatry 55 (2): 70–6. PMID 8077157.

Ener RA, Meglathery SB, Styler M (xuño de 2004). "Extravasation of systemic hemato-oncological therapies". Ann Oncol 15 (6): 858–62. PMID 15151940. doi:10.1093/annonc/mdh214.

ox.ac.uk (Global: 613^th place; Galician: 779^th place)

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"Low Gene Copy Number for C4, C4A and C4B Is a Strong Risk Factor for Developing Systemic Lupus Erythematosus in Childhood". Arquivado dende o orixinal o 25 de outubro de 2023. Consultado o 25 de outubro de 2023.

"Dr. Sharon B. Meglathery MD". Arquivado dende o orixinal o 15 de novembro de 2023. Consultado o 8 de marzo de 2024. A Dra. Sharon B. Meglathery é psiquiatra en Tucson, Arizona. Recibiu o seu grao en medicina da Oregon Health and Science University School of Medicine

"The RCCX theory of chronic illness". Arquivado dende o orixinal o 10 de decembro de 2023. Consultado o 8 de marzo 2024.

TNP210 RCCX Theory of Complex Illness. Arquivado dende o orixinal o 14 de novembro de 2023. Consultado o 8 de marzo de 2024 – vía www.audible.com.

"Hypermobility, RCCX Theory and One Journey from Illness Towards Wholeness". Arquivado dende o orixinal o 14 de decembro de 2023. Consultado o 8 de marzo de 2024.

RCCX (Galician Wikipedia)

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RCCX (Galician Wikipedia)

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