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Annals of Surgical Oncology|June 13, 2020
The Devil's in the Details: Discrepancy Between Biopsy Thickness and Final Pathology in Acral MelanomaAnn Y Lee, Erica B Friedman, James Sun, et al.
Infection and Immunity|January 27, 2010
Staphylococcus aureus fur regulates the expression of virulence factors that contribute to the pathogenesis of pneumoniaVictor J Torres, Ahmed S Attia, William J Mason, et al.
Genomics|November 24, 1999
Characterization of the human and mouse unconventional myosin XV genes responsible for hereditary deafness DFNB3 and shaker 2Y Liang, A Wang, I A Belyantseva, et al.
Journal of Medical Genetics|April 3, 2004
A locus for spondylocarpotarsal synostosis syndrome at chromosome 3p14C Steiner, N Ehtesham, K D Taylor, et al.
BMC Medical Genetics|September 28, 2004
Characterization of a new full length TMPRSS3 isoform and identification of mutant alleles responsible for nonsyndromic recessive deafness in Newfoundland and PakistanZubair M Ahmed, Xiaoyan Cindy Li, Shontell D Powell, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 11, 2020
Noncoding Microdeletion in Mouse Hgf Disrupts Neural Crest Migration into the Stria Vascularis, Reduces the Endocochlear Potential, and Suggests the Neuropathology for Human Nonsyndromic Deafness DFNB39Robert J Morell, Rafal Olszewski, Risa Tona, et al.
American Journal of Human Genetics|December 28, 2010
Functional null mutations of MSRB3 encoding methionine sulfoxide reductase are associated with human deafness DFNB74Zubair M Ahmed, Rizwan Yousaf, Byung Cheon Lee, et al.
Molecular Endocrinology (Baltimore, Md.)|May 8, 2014
NFI transcription factors interact with FOXA1 to regulate prostate-specific gene expressionMagdalena M Grabowska, Amicia D Elliott, David J DeGraff, et al.
American Journal of Human Genetics|December 31, 2005
Mutations in TRIOBP, which encodes a putative cytoskeletal-organizing protein, are associated with nonsyndromic recessive deafnessSaima Riazuddin, Shaheen N Khan, Zubair M Ahmed, et al.
Human Mutation|January 9, 2008
Mutation spectrum of MYO7A and evaluation of a novel nonsyndromic deafness DFNB2 allele with residual functionSaima Riazuddin, Sabiha Nazli, Zubair M Ahmed, et al.
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