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Select item 101967091.

A complex structural variant near SOX3 causes X-linked split-hand/foot malformation

Elke de Boer, Carlo Marcelis, Kornelia Neveling, Ellen van Beusekom, Alexander Hoischen, Willemijn M. Klein, Nicole de Leeuw, Tuomo Mantere, Uirá S. Melo, Jeroen van Reeuwijk, Dominique Smeets, Malte Spielmann, Tjitske Kleefstra, Hans van Bokhoven, Lisenka E.L.M. Vissers

HGG Adv. 2023 Jul 13; 4(3): 100200. Published online 2023 Apr 25. doi: 10.1016/j.xhgg.2023.100200

PMCID:: PMC10196709

Article PDF–4.1M

Select item 72997282.

Serum proteome profiling reveals SOX3 as a candidate prognostic marker for gastric cancer

Jiajia Shen, Jing Zhai, Xinqian Wu, Guiping Xie, Lizong Shen

J Cell Mol Med. 2020 Jun; 24(12): 6750–6761. Published online 2020 May 4. doi: 10.1111/jcmm.15326

PMCID:: PMC7299728

Article PDF–1.4M

Select item 55908773.

Epigenetic regulation of human SOX3 gene expression during early phases of neural differentiation of NT2/D1 cells

Vladanka Topalovic, Aleksandar Krstic, Marija Schwirtlich, Diletta Dolfini, Roberto Mantovani, Milena Stevanovic, Marija Mojsin

PLoS One. 2017; 12(9): e0184099. Published online 2017 Sep 8. doi: 10.1371/journal.pone.0184099

PMCID:: PMC5590877

Article PDF–21M

Select item 17358984.

Array comparative genomic hybridisation analysis of boys with X linked hypopituitarism identifies a 3.9 Mb duplicated critical region at Xq27 containing SOX3

N Solomon, S Ross, T Morgan, J Belsky, F Hol, P Karnes, N Hopwood, S Myers, A Tan, G Warne, S Forrest, P Thomas

J Med Genet. 2004 Sep; 41(9): 669–678. doi: 10.1136/jmg.2003.016949

PMCID:: PMC1735898

Summary PDF–240K

Select item 17124625.

X-linked recessive panhypopituitarism associated with a regional duplication in Xq25-q26.

M Lagerström-Fermér, M Sundvall, E Johnsen, G L Warne, S M Forrest, J D Zajac, A Rickards, D Ravine, U Landegren, U Pettersson

Am J Hum Genet. 1997 Apr; 60(4): 910–916.

PMCID:: PMC1712462

Summary Page Browse PDF–1.2M

Select item 11993726.

Over- and Underdosage of SOX3 Is Associated with Infundibular Hypoplasia and Hypopituitarism

Kathryn S. Woods, Maria Cundall, James Turton, Karine Rizotti, Ameeta Mehta, Rodger Palmer, Jacqueline Wong, W. K. Chong, Mahmoud Al-Zyoud, Maryam El-Ali, Timo Otonkoski, Juan-Pedro Martinez-Barbera, Paul Q. Thomas, Iain C. Robinson, Robin Lovell-Badge, Karen J. Woodward, Mehul T. Dattani

Am J Hum Genet. 2005 May; 76(5): 833–849. Published online 2005 Mar 30. doi: 10.1086/430134

PMCID:: PMC1199372

Article PDF–851K

Select item 53647147.

Sex-determining region Y-box protein 3 induces epithelial-mesenchymal transition in osteosarcoma cells via transcriptional activation of Snail1

Manle Qiu, Daoyun Chen, Chaoyong Shen, Ji Shen, Huakun Zhao, Yaohua He

J Exp Clin Cancer Res. 2017; 36: 46. Published online 2017 Mar 23. doi: 10.1186/s13046-017-0515-3

PMCID:: PMC5364714

Article PDF–7.2M

Select item 31132468.

X-Linked Congenital Hypertrichosis Syndrome Is Associated with Interchromosomal Insertions Mediated by a Human-Specific Palindrome near SOX3

Hongwen Zhu, Dandan Shang, Miao Sun, Sunju Choi, Qing Liu, Jiajie Hao, Luis E. Figuera, Feng Zhang, Kwong Wai Choy, Yang Ao, Yang Liu, Xiao-Lin Zhang, Fengzhen Yue, Ming-Rong Wang, Li Jin, Pragna I. Patel, Tao Jing, Xue Zhang

Am J Hum Genet. 2011 Jun 10; 88(6): 819–826. doi: 10.1016/j.ajhg.2011.05.004

PMCID:: PMC3113246

Article PDF–884K

Select item 2623339.

Sox3 Is Required for Gonadal Function, but Not Sex Determination, in Males and Females

Jeffrey Weiss, Joshua J. Meeks, Lisa Hurley, Gerald Raverot, Andrea Frassetto, J. Larry Jameson

Mol Cell Biol. 2003 Nov; 23(22): 8084–8091. doi: 10.1128/MCB.23.22.8084-8091.2003

PMCID:: PMC262333

Article PDF–449K

Select item 839426010.

Allelic Variants in Established Hypopituitarism Genes Expand Our Knowledge of the Phenotypic Spectrum

Marilena Nakaguma, Nathalia Garcia Bianchi Pereira Ferreira, Anna Flavia Figueredo Benedetti, Mariana Cotarelli Madi, Juliana Moreira Silva, Jun Z. Li, Qianyi Ma, Ayse Bilge Ozel, Qing Fang, Amanda de Moraes Narcizo, Laís Cavalca Cardoso, Luciana Ribeiro Montenegro, Mariana Ferreira de Assis Funari, Mirian Yumie Nishi, Ivo Jorge Prado Arnhold, Alexander Augusto de Lima Jorge, Berenice Bilharinho de Mendonca, Sally Ann Camper, Luciani R. Carvalho

Genes (Basel) 2021 Aug; 12(8): 1128. Published online 2021 Jul 25. doi: 10.3390/genes12081128

PMCID:: PMC8394260

Article PDF–2.3M

Select item 479511211.

Testis development in the absence of SRY: chromosomal rearrangements at SOX9 and SOX3

Annalisa Vetro, Mohammad Reza Dehghani, Lilia Kraoua, Roberto Giorda, Silvana Beri, Laura Cardarelli, Maurizio Merico, Emmanouil Manolakos, Alexis Parada-Bustamante, Andrea Castro, Orietta Radi, Giovanna Camerino, Alfredo Brusco, Marjan Sabaghian, Crystalena Sofocleous, Francesca Forzano, Pietro Palumbo, Orazio Palumbo, Savino Calvano, Leopoldo Zelante, Paola Grammatico, Sabrina Giglio, Mohamed Basly, Myriam Chaabouni, Massimo Carella, Gianni Russo, Maria Clara Bonaglia, Orsetta Zuffardi

Eur J Hum Genet. 2015 Aug; 23(8): 1025–1032. Published online 2014 Nov 5. doi: 10.1038/ejhg.2014.237

PMCID:: PMC4795112

Article PDF–2.2M

Select item 416389412.

Cyclic AMP response element binding (CREB) protein acts as a positive regulator of SOX3 gene expression in NT2/D1 cells

Natasa Kovacevic-Grujicic, Marija Mojsin, Jelena Popovic, Isidora Petrovic, Vladanka Topalovic, Milena Stevanovic

BMB Rep. 2014 Apr; 47(4): 197–202. doi: 10.5483/BMBRep.2014.47.4.084

PMCID:: PMC4163894

Article PDF–3.2M

Select item 42000413.

Transcription Factor SOX3 Is Involved in X-Linked Mental Retardation with Growth Hormone Deficiency

Frédéric Laumonnier, Nathalie Ronce, Ben C. J. Hamel, Paul Thomas, James Lespinasse, Martine Raynaud, Christine Paringaux, Hans van Bokhoven, Vera Kalscheuer, Jean-Pierre Fryns, Jamel Chelly, Claude Moraine, Sylvain Briault

Am J Hum Genet. 2002 Dec; 71(6): 1450–1455. Published online 2002 Nov 8. doi: 10.1086/344661

PMCID:: PMC420004

Article PDF–307K

Select item 1066064314.

ROR2 deficit may induce the tetralogy of Fallot via down‐regulating of β‐catenin/SOX3/HSPA6 in vitro and in vivo

Rui Guo, Yiran Zhou Guo, Qing Zhou, Guoju Li, Zhanghui Du, Yefei Shi, Quansheng Xing

J Cell Mol Med. 2023 Nov; 27(22): 3539–3552. Published online 2023 Sep 25. doi: 10.1111/jcmm.17969

PMCID:: PMC10660643

Article PDF–11M

Select item 114241415.

SUMO Represses Transcriptional Activity of the Drosophila SoxNeuro and Human Sox3 Central Nervous System–specific Transcription Factors

Jean Savare, Nathalie Bonneaud, Franck Girard

Mol Biol Cell. 2005 Jun; 16(6): 2660–2669. doi: 10.1091/mbc.E04-12-1062

PMCID:: PMC1142414

Article PDF–371K

Select item 300714116.

Identification of SOX3 as an XX male sex reversal gene in mice and humans

Edwina Sutton, James Hughes, Stefan White, Ryohei Sekido, Jacqueline Tan, Valerie Arboleda, Nicholas Rogers, Kevin Knower, Lynn Rowley, Helen Eyre, Karine Rizzoti, Dale McAninch, Joao Goncalves, Jennie Slee, Erin Turbitt, Damien Bruno, Henrik Bengtsson, Vincent Harley, Eric Vilain, Andrew Sinclair, Robin Lovell-Badge, Paul Thomas

J Clin Invest. 2011 Jan 4; 121(1): 328–341. Published online 2010 Dec 22. doi: 10.1172/JCI42580

PMCID:: PMC3007141

Article PDF–8.0M

Select item 374087217.

SOX2–LIN28/let-7 pathway regulates proliferation and neurogenesis in neural precursors

Flavio Cimadamore, Alejandro Amador-Arjona, Connie Chen, Chun-Teng Huang, Alexey V. Terskikh

Proc Natl Acad Sci U S A. 2013 Aug 6; 110(32): E3017–E3026. Published online 2013 Jul 24. doi: 10.1073/pnas.1220176110

PMCID:: PMC3740872

Article PDF–1.8M

Select item 33693918.

A conserved family of genes related to the testis determining gene, SRY.

P Denny, S Swift, N Brand, N Dabhade, P Barton, A Ashworth

Nucleic Acids Res. 1992 Jun 11; 20(11): 2887. doi: 10.1093/nar/20.11.2887

PMCID:: PMC336939

Summary Page Browse PDF–198K

Select item 633388319.

Proteolysis of methylated SOX2 protein is regulated by L3MBTL3 and CRL4^DCAF5 ubiquitin ligase

Chunxiao Zhang, Feng Leng, Lovely Saxena, Nam Hoang, Jiekai Yu, Salvador Alejo, Logan Lee, Dandan Qi, Fei Lu, Hong Sun, Hui Zhang

J Biol Chem. 2019 Jan 11; 294(2): 476–489. Published online 2018 Nov 15. doi: 10.1074/jbc.RA118.005336

PMCID:: PMC6333883

Article PDF–3.1M

Select item 966758620.

ARPC1B promotes mesenchymal phenotype maintenance and radiotherapy resistance by blocking TRIM21-mediated degradation of IFI16 and HuR in glioma stem cells

Zijie Gao, Jianye Xu, Yang Fan, Zongpu Zhang, Huizhi Wang, Mingyu Qian, Ping Zhang, Lin Deng, Jie Shen, Hao Xue, Rongrong Zhao, Teng Zhou, Xing Guo, Gang Li

J Exp Clin Cancer Res. 2022; 41: 323. Published online 2022 Nov 16. doi: 10.1186/s13046-022-02526-8

PMCID:: PMC9667586

Article PDF–11M

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