Ohcanbohtosat - Ethylin Wang Jabs
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Genetic basis of potential therapeutic strategies for craniosynostosis Dahkki Heather Melville, Yingli Wang, Peter J. Taub, Ethylin Wang Jabs
Almmustuhtton 2010Revisão -
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The human aquaporin-CHIP gene. Structure, organization, and chromosomal localization Dahkki Chulso Moon, Gregory M. Preston, C.A. Griffin, Ethylin Wang Jabs, Peter Agre
Almmustuhtton 1993Artigo -
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FGF/FGFR Signaling Coordinates Skull Development by Modulating Magnitude of Morphological Integration: Evidence from Apert Syndrome Mouse Models Dahkki Neus Martínez‐Abadías, Yann Heuzé, Yingli Wang, Ethylin Wang Jabs, Kristina Aldridge, Joan T. Richtsmeier
Almmustuhtton 2011Artigo -
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Development and preliminary evaluation of an online educational video about whole-genome sequencing for research participants, patients, and the general public Dahkki Saskia C. Sanderson, Sabrina A. Suckiel, Micol Zweig, Erwin P. Böttinger, Ethylin Wang Jabs, Lynne D. Richardson
Almmustuhtton 2015Artigo -
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Mapping the Treacher Collins syndrome locus to 5q31.3→q33.3 Dahkki Ethylin Wang Jabs, Xiang Li, Cathleen A. Coss, Eugene W. Taylor, Deborah A. Meyers, James L. Weber
Almmustuhtton 1991Artigo -
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Clinical spectrum of fibroblast growth factor receptor mutations Dahkki M.R. Passos-Bueno, W.R. Wilcox, Ethylin Wang Jabs, Andréa L. Sertié, Luís Garcia Alonso, H. Kitoh
Almmustuhtton 1999Artigo -
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The Ups and Downs of Mutation Frequencies during Aging Can Account for the Apert Syndrome Paternal Age Effect Dahkki Song-Ro Yoon, Jian Qin, Rivka L. Glaser, Ethylin Wang Jabs, Nancy S. Wexler, Rebecca Z. Sokol, Norman Arnheim, Peter Calabrese
Almmustuhtton 2009Artigo -
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<i>TCOF1</i> gene encodes a putative nucleolar phosphoprotein that exhibits mutations in Treacher Collins Syndrome throughout its coding region Dahkki Carol A. Wise, Lydia C. Chiang, William A. Paznekas, Mridula Sharma, Maurice M. Musy, Jennifer Ashley, Michael Lovett, Ethylin Wang Jabs
Almmustuhtton 1997Artigo -
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Advancing age has differential effects on DNA damage, chromatin integrity, gene mutations, and aneuploidies in sperm Dahkki Andrew J. Wyrobek, Brenda Eskenazi, Suzanne Young, Norman Arnheim, Irene Tiemann‐Boege, Ethylin Wang Jabs, Rivka L. Glaser, Francesca Pearson, D.P. Evenson
Almmustuhtton 2006Artigo
Ohcanreaiddut:
Laktáseaddji fáttát
Biology
Genetics
Gene
Medicine
Mutation
Phenotype
Craniosynostosis
Craniofacial
Internal medicine
Receptor
Cell biology
Genotype
Missense mutation
Fibroblast growth factor
Molecular biology
Anatomy
Apert syndrome
Fibroblast growth factor receptor
Biochemistry
Chromosome
Genome
Pathology
Allele
Computer science
Connexin
Endocrinology
Fibroblast growth factor receptor 1
Gap junction
Intracellular
Mutant