PMC Links for Protein (Select 116734702) - PMC

Select item 55417861.

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

Select item 51730952.

The posterior HOXD locus: Its contribution to phenotype and malignancy of Ewing sarcoma

Kristina von Heyking, Laura Roth, Miriam Ertl, Oxana Schmidt, Julia Calzada-Wack, Frauke Neff, Elizabeth R. Lawlor, Stefan Burdach, Günther H.S. Richter

Oncotarget. 2016 Jul 5; 7(27): 41767–41780. Published online 2016 May 30. doi: 10.18632/oncotarget.9702

PMCID:: PMC5173095

Abstract Article PDF–8.9M

Select item 46376833.

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

Abstract Article PDF–662K

Select item 13775024.

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

Summary PDF–828K

Select item 3353085.

The human HOX gene family.

D Acampora, M D'Esposito, A Faiella, M Pannese, E Migliaccio, F Morelli, A Stornaiuolo, V Nigro, A Simeone, E Boncinelli

Nucleic Acids Res. 1989 Dec 25; 17(24): 10385–10402. doi: 10.1093/nar/17.24.10385

PMCID:: PMC335308

Summary Page Browse PDF–1.6M

Select item 44579566.

Individualized Iterative Phenotyping for Genome-wide Analysis of Loss-of-Function Mutations

Jennifer J. Johnston, Katie L. Lewis, David Ng, Larry N. Singh, Jamila Wynter, Carmen Brewer, Brian P. Brooks, Isaac Brownell, Fabio Candotti, Steven G. Gonsalves, Suzanne P. Hart, Heidi H. Kong, Kristina I. Rother, Robert Sokolic, Benjamin D. Solomon, Wadih M. Zein, David N. Cooper, Peter D. Stenson, James C. Mullikin, Leslie G. Biesecker

Am J Hum Genet. 2015 Jun 4; 96(6): 913–925. doi: 10.1016/j.ajhg.2015.04.013

PMCID:: PMC4457956

Abstract Article PDF–219K

Select item 40068677.

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

Abstract Article PDF–828K

Select item 35355068.

Anorectal atresia and variants at predicted regulatory sites in candidate genes

Tonia C. Carter, Denise M. Kay, Marilyn L. Browne, Aiyi Liu, Paul A. Romitti, Devon Kuehn, Mary R. Conley, Michele Caggana, Charlotte M. Druschel, Lawrence C. Brody, James L. Mills

Ann Hum Genet. Author manuscript; available in PMC 2014 Jan 1.

Published in final edited form as: Ann Hum Genet. 2013 Jan; 77(1): 31–46. Published online 2012 Nov 6. doi: 10.1111/j.1469-1809.2012.00734.x

PMCID:: PMC3535506

Abstract Article PDF–110K

PMC

Result Filters

Article attributes

Text availability

Publication date

Custom date range

Research Funder

Additional filters

Display Settings:

Send to:

Links from Protein

Items: 8

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity