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Items: 1 to 20 of 44

1.
Identification of a HOXD13 variant in a Mongolian family with incomplete penetrance syndactyly by exon sequencing
Husile Husile, Zhifeng Wu, Liqing Yang, Yaning Cao, Qizhu Wu
BMC Med Genomics. 2022; 15: 210. Published online 2022 Oct 4. doi: 10.1186/s12920-022-01360-3
PMCID:
PMC9533607
AbstractArticlePDF–1.4M
2.
Prognostic significance of HOXD13 expression in human breast cancer
Zhen-Bin Zhong, Ming Shan, Cheng Qian, Tong Liu, Qing-Yu Shi, Ji Wang, Yan Liu, Yang Liu, Yuan-Xi Huang, Da Pang
Int J Clin Exp Pathol. 2015; 8(9): 11407–11413. Published online 2015 Sep 1.
PMCID:
PMC4637683
AbstractArticlePDF–662K
3.
HOXD13 methylation status is a prognostic indicator in breast cancer
Zhenbin Zhong, Ming Shan, Ji Wang, Tong Liu, Bingshu Xia, Ming Niu, Yanlv Ren, Da Pang
Int J Clin Exp Pathol. 2015; 8(9): 10716–10724. Published online 2015 Sep 1.
PMCID:
PMC4637597
AbstractArticlePDF–1.1M
4.
Synpolydactyly and HOXD13 polyalanine repeat: addition of 2 alanine residues is without clinical consequences
Sajid Malik, KM Girisha, Muhammad Wajid, Akhilesh K Roy, Shubha R Phadke, Sayedul Haque, Wasim Ahmad, Manuela C Koch, Karl-Heinz Grzeschik
BMC Med Genet. 2007; 8: 78. Published online 2007 Dec 11. doi: 10.1186/1471-2350-8-78
PMCID:
PMC2222244
AbstractArticlePDF–1.0M
5.
Deletions in HOXD13 segregate with an identical, novel foot malformation in two unrelated families.
F Goodman, M L Giovannucci-Uzielli, C Hall, W Reardon, R Winter, P Scambler
Am J Hum Genet. 1998 Oct; 63(4): 992–1000. doi: 10.1086/302070
PMCID:
PMC1377502
SummaryPDF–828K
6.
Variants Identified in the HOXC13 and HOXD13 Genes Suggest Association with Cervical Cancer in a Cohort of Mexican Women
Karina Janett Juárez-Rendón, Manuel Alejandro Castro-García, Diddier Giovanni Prada-Ortega, Gildardo Rivera, Luz María Ruíz-Godoy, Virginia Isabel Enríquez-Cárcamo, Miguel Angel Reyes-Lopez
Genes (Basel) 2023 Feb; 14(2): 358. Published online 2023 Jan 30. doi: 10.3390/genes14020358
PMCID:
PMC9957514
AbstractArticlePDF–693K
7.
HOXD13 promotes the malignant progression of colon cancer by upregulating PTPRN2
Jiangyan Yin, Yi Guo
Cancer Med. 2021 Aug; 10(16): 5524–5533. Published online 2021 Jul 17. doi: 10.1002/cam4.4078
PMCID:
PMC8366098
AbstractArticlePDF–2.1M
8.
Genome sequencing in families with congenital limb malformations
Jonas Elsner, Martin A. Mensah, Manuel Holtgrewe, Jakob Hertzberg, Stefania Bigoni, Andreas Busche, Marie Coutelier, Deepthi C. de Silva, Nursel Elçioglu, Isabel Filges, Erica Gerkes, Katta M. Girisha, Luitgard Graul-Neumann, Aleksander Jamsheer, Peter Krawitz, Ingo Kurth, Susanne Markus, Andre Megarbane, André Reis, Miriam S. Reuter, Daniel Svoboda, Christopher Teller, Beyhan Tuysuz, Seval Türkmen, Meredith Wilson, Rixa Woitschach, Inga Vater, Almuth Caliebe, Wiebke Hülsemann, Denise Horn, Stefan Mundlos, Malte Spielmann
Hum Genet. 2021; 140(8): 1229–1239. Published online 2021 Jun 22. doi: 10.1007/s00439-021-02295-y
PMCID:
PMC8263393
AbstractArticlePDF–7.1M
9.
A novel miR-7156-3p-HOXD13 axis modulates glioma progression by regulating tumor cell stemness
Junfeng Zhang, Mengsheng Deng, Haipeng Tong, Wei Xue, Yu Guo, Jianmin Wang, Lizhao Chen, Shunan Wang
Int J Biol Sci. 2020; 16(16): 3200–3209. Published online 2020 Oct 21. doi: 10.7150/ijbs.51293
PMCID:
PMC7645993
AbstractArticlePDF–3.4M
10.
A nonsense mutation in the HOXD13 gene underlies synpolydactyly with incomplete penetrance
Mazen Kurban, Muhammad Wajid, Lynn Petukhova, Yutaka Shimomura, Angela M Christiano
J Hum Genet. Author manuscript; available in PMC 2015 Jan 16.
Published in final edited form as: J Hum Genet. 2011 Oct; 56(10): 701–706. Published online 2011 Aug 4. doi: 10.1038/jhg.2011.84
PMCID:
PMC4296310
AbstractArticlePDF–898K
11.
Mutations in the Homeodomain of HOXD13 Cause Syndactyly Type 1-c in Two Chinese Families
Limeng Dai, Dan Liu, Min Song, Xueqing Xu, Gang Xiong, Kang Yang, Kun Zhang, Hui Meng, Hong Guo, Yun Bai
PLoS One. 2014; 9(5): e96192. Published online 2014 May 1. doi: 10.1371/journal.pone.0096192
Correction in:
PLoS One. 2014; 9(7): e104309.
PMCID:
PMC4006867
AbstractArticlePDF–828K
12.
Isolated brachydactyly type E caused by a HOXD13 nonsense mutation: a case report
Aleksander Jamsheer, Anna Sowińska, Leszek Kaczmarek, Anna Latos-Bieleńska
BMC Med Genet. 2012; 13: 4. Published online 2012 Jan 10. doi: 10.1186/1471-2350-13-4
PMCID:
PMC3278352
AbstractArticlePDF–323K
13.
HOXD13 Binds DNA Replication Origins To Promote Origin Licensing and Is Inhibited by Geminin
Valentina Salsi, Silvia Ferrari, Roberta Ferraresi, Andrea Cossarizza, Alexis Grande, Vincenzo Zappavigna
Mol Cell Biol. 2009 Nov; 29(21): 5775–5788. Published online 2009 Aug 24. doi: 10.1128/MCB.00509-09
PMCID:
PMC2772751
AbstractArticlePDF–2.4M
14.
Severe digital abnormalities in a patient heterozygous for both a novel missense mutation in HOXD13 and a polyalanine tract expansion in HOXA13
P Debeer, C Bacchelli, P Scambler, L De Smet, J Fryns, F Goodman
J Med Genet. 2002 Nov; 39(11): 852–856. doi: 10.1136/jmg.39.11.852
PMCID:
PMC1735011
SummaryPDF–172K
15.
Missense Mutations in the Homeodomain of HOXD13 Are Associated with Brachydactyly Types D and E
David Johnson, Shih-hsin Kan, Michael Oldridge, Richard C. Trembath, Philippe Roche, Robert M. Esnouf, Henk Giele, Andrew O. M. Wilkie
Am J Hum Genet. 2003 Apr; 72(4): 984–997. Published online 2003 Mar 14. doi: 10.1086/374721
PMCID:
PMC1180360
AbstractArticlePDF–893K
16.
Synpolydactyly phenotypes correlate with size of expansions in HOXD13 polyalanine tract
F. R. Goodman, S. Mundlos, Y. Muragaki, D. Donnai, M. L. Giovannucci-Uzielli, E. Lapi, F. Majewski, J. McGaughran, C. McKeown, W. Reardon, J. Upton, R. M. Winter, B. R. Olsen, P. J. Scambler
Proc Natl Acad Sci U S A. 1997 Jul 8; 94(14): 7458–7463. doi: 10.1073/pnas.94.14.7458
PMCID:
PMC23843
AbstractArticlePDF–327K
17.
EWS::FLI1 and HOXD13 control tumor cell plasticity in Ewing sarcoma
April A. Apfelbaum, Feinan Wu, Allegra G. Hawkins, Brian Magnuson, Jennifer A. Jiménez, Sean D. Taylor, Emma D. Wrenn, Olivia Waltner, Elise R. Pfaltzgraff, Jane Y. Song, Cody Hall, Deneen M. Wellik, Mats Ljungman, Scott N. Furlan, Russell J.H. Ryan, Jay F. Sarthy, Elizabeth R. Lawlor
Clin Cancer Res. Author manuscript; available in PMC 2023 Apr 14.
Published in final edited form as: Clin Cancer Res. 2022 Oct 14; 28(20): 4466–4478. doi: 10.1158/1078-0432.CCR-22-0384
PMCID:
PMC9588607
AbstractArticlePDF–2.5M
18.
Mutant Idh2 cooperates with a NUP98-HOXD13 fusion to induce early immature thymocyte precursor ALL
Liat Goldberg, Vijay Negi, Yang Jo Chung, Masahiro Onozawa, Yuelin J. Zhu, Robert L. Walker, Rachel Pierce, Daxesh P. Patel, Kristopher W. Krausz, Frank J. Gonzalez, Margaret A. Goodell, Benjamin A.T. Rodriguez, Paul S. Meltzer, Peter D. Aplan
Cancer Res. Author manuscript; available in PMC 2022 Apr 1.
Published in final edited form as: Cancer Res. 2021 Oct 1; 81(19): 5033–5046. Published online 2021 Jul 28. doi: 10.1158/0008-5472.CAN-21-1027
PMCID:
PMC8487989
AbstractArticlePDF–2.4M
19.
HOXB9 Expression Correlates with Histological Grade and Prognosis in LSCC
Chuanhui Sun, Changsong Han, Peng Wang, Yinji Jin, Yanan Sun, Lingmei Qu
Biomed Res Int. 2017; 2017: 3680305. Published online 2017 Jul 20. doi: 10.1155/2017/3680305
PMCID:
PMC5541786
AbstractArticlePDF–2.1M
20.
Oxidative stress leads to increased mutation frequency in a murine model of myelodysplastic syndrome
Yang Jo Chung, Carine Robert, Sheryl M. Gough, Feyruz V. Rassool, Peter D. Aplan
Leuk Res. Author manuscript; available in PMC 2015 Jan 1.
Published in final edited form as: Leuk Res. 2014 Jan; 38(1): 10.1016/j.leukres.2013.07.008. Published online 2013 Aug 16. doi: 10.1016/j.leukres.2013.07.008
PMCID:
PMC3872269
AbstractArticlePDF–2.2M

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