ساکس ۶ (Persian Wikipedia)

Analysis of information sources in references of the Wikipedia article "ساکس ۶" in Persian language version.

refsWebsite

Global rank Persian rank

11nih.gov

4^th place

5^th place

7doi.org

2^nd place

1ensembl.org

1,626^th place

1,252^nd place

1semanticscholar.org

11^th place

52^nd place

1harvard.edu

18^th place

50^th place

1wiley.com

222^nd place

185^th place

doi.org

Cohen-Barak O, Hagiwara N, Arlt MF, Horton JP, Brilliant MH (March 2001). "Cloning, characterization and chromosome mapping of the human SOX6 gene". Gene. 265 (1–2): 157–164. doi:10.1016/S0378-1119(01)00346-8. PMID 11255018.
Murakami A, Ishida S, Thurlow J, Revest JM, Dickson C (August 2001). "SOX6 binds CtBP2 to repress transcription from the Fgf-3 promoter". Nucleic Acids Research. 29 (16): 3347–3355. doi:10.1093/nar/29.16.3347. PMC 55854. PMID 11504872.
Yamashita A, Ito M, Takamatsu N, Shiba T (September 2000). "Characterization of Solt, a novel SoxLZ/Sox6 binding protein expressed in adult mouse testis". FEBS Letters. 481 (2): 147–151. doi:10.1016/S0014-5793(00)01987-6. PMID 10996314. S2CID 20831354.
Cantù C, Ierardi R, Alborelli I, Fugazza C, Cassinelli L, Piconese S, et al. (March 2011). "Sox6 enhances erythroid differentiation in human erythroid progenitors". Blood. 117 (13): 3669–3679. doi:10.1182/blood-2010-04-282350. PMID 21263153.
Marchetto A, Ohmura S, Orth MF, Knott MM, Colombo MV, Arrigoni C, et al. (May 2020). "Oncogenic hijacking of a developmental transcription factor evokes vulnerability toward oxidative stress in Ewing sarcoma". Nature Communications. 11 (1): 2423. Bibcode:2020NatCo..11.2423M. doi:10.1038/s41467-020-16244-2. PMC 7228971. PMID 32415069.
Tolchin, Dara, et al. (2020). "De Novo SOX6 Variants Cause a Neurodevelopmental Syndrome Associated with ADHD, Craniosynostosis, and Osteochondromas". American Journal of Human Genetics. 6 (106): 830–845. doi:10.1016/j.ajhg.2020.04.015.
Schneider, Susanne A.; Mueller, Christine; Biskup, Saskia; Fietzek, Urban M.; Schroeder, Andreas Sebastian (2022). "Neurodevelopmental disorder with dystonia due to SOX6 mutations". Molecular Genetics & Genomic Medicine. 10 (12): 1–5. doi:10.1002/mgg3.2051.

ensembl.org

May2017.archive.ensembl.org

GRCm38: Ensembl release 89: ENSMUSG00000051910 - Ensembl, May 2017

harvard.edu

ui.adsabs.harvard.edu

Marchetto A, Ohmura S, Orth MF, Knott MM, Colombo MV, Arrigoni C, et al. (May 2020). "Oncogenic hijacking of a developmental transcription factor evokes vulnerability toward oxidative stress in Ewing sarcoma". Nature Communications. 11 (1): 2423. Bibcode:2020NatCo..11.2423M. doi:10.1038/s41467-020-16244-2. PMC 7228971. PMID 32415069.

nih.gov

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: SOX6 SRY (sex determining region Y)-box 6".
Murakami A, Ishida S, Thurlow J, Revest JM, Dickson C (August 2001). "SOX6 binds CtBP2 to repress transcription from the Fgf-3 promoter". Nucleic Acids Research. 29 (16): 3347–3355. doi:10.1093/nar/29.16.3347. PMC 55854. PMID 11504872.
Marchetto A, Ohmura S, Orth MF, Knott MM, Colombo MV, Arrigoni C, et al. (May 2020). "Oncogenic hijacking of a developmental transcription factor evokes vulnerability toward oxidative stress in Ewing sarcoma". Nature Communications. 11 (1): 2423. Bibcode:2020NatCo..11.2423M. doi:10.1038/s41467-020-16244-2. PMC 7228971. PMID 32415069.
Tolchin, Dara, et al. (2020). "De Novo SOX6 Variants Cause a Neurodevelopmental Syndrome Associated with ADHD, Craniosynostosis, and Osteochondromas". American Journal of Human Genetics. 6 (106): 830–845. doi:10.1016/j.ajhg.2020.04.015.

pubmed.ncbi.nlm.nih.gov

Cohen-Barak O, Hagiwara N, Arlt MF, Horton JP, Brilliant MH (March 2001). "Cloning, characterization and chromosome mapping of the human SOX6 gene". Gene. 265 (1–2): 157–164. doi:10.1016/S0378-1119(01)00346-8. PMID 11255018.
Murakami A, Ishida S, Thurlow J, Revest JM, Dickson C (August 2001). "SOX6 binds CtBP2 to repress transcription from the Fgf-3 promoter". Nucleic Acids Research. 29 (16): 3347–3355. doi:10.1093/nar/29.16.3347. PMC 55854. PMID 11504872.
Yamashita A, Ito M, Takamatsu N, Shiba T (September 2000). "Characterization of Solt, a novel SoxLZ/Sox6 binding protein expressed in adult mouse testis". FEBS Letters. 481 (2): 147–151. doi:10.1016/S0014-5793(00)01987-6. PMID 10996314. S2CID 20831354.
Cantù C, Ierardi R, Alborelli I, Fugazza C, Cassinelli L, Piconese S, et al. (March 2011). "Sox6 enhances erythroid differentiation in human erythroid progenitors". Blood. 117 (13): 3669–3679. doi:10.1182/blood-2010-04-282350. PMID 21263153.
Marchetto A, Ohmura S, Orth MF, Knott MM, Colombo MV, Arrigoni C, et al. (May 2020). "Oncogenic hijacking of a developmental transcription factor evokes vulnerability toward oxidative stress in Ewing sarcoma". Nature Communications. 11 (1): 2423. Bibcode:2020NatCo..11.2423M. doi:10.1038/s41467-020-16244-2. PMC 7228971. PMID 32415069.

semanticscholar.org

api.semanticscholar.org

Yamashita A, Ito M, Takamatsu N, Shiba T (September 2000). "Characterization of Solt, a novel SoxLZ/Sox6 binding protein expressed in adult mouse testis". FEBS Letters. 481 (2): 147–151. doi:10.1016/S0014-5793(00)01987-6. PMID 10996314. S2CID 20831354.

wiley.com

onlinelibrary.wiley.com

Schneider, Susanne A.; Mueller, Christine; Biskup, Saskia; Fietzek, Urban M.; Schroeder, Andreas Sebastian (2022). "Neurodevelopmental disorder with dystonia due to SOX6 mutations". Molecular Genetics & Genomic Medicine. 10 (12): 1–5. doi:10.1002/mgg3.2051.