Ngā hua rapu - Ethylin Wang Jabs
- E whakaatu ana i te 1 - 20 hua o te 67
- Haere ki te Whārangi Whai Ake
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Genetic basis of potential therapeutic strategies for craniosynostosis mā Heather Melville, Yingli Wang, Peter J. Taub, Ethylin Wang Jabs
I whakaputaina 2010Revisão -
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FGF/FGFR Signaling Coordinates Skull Development by Modulating Magnitude of Morphological Integration: Evidence from Apert Syndrome Mouse Models mā Neus Martínez‐Abadías, Yann Heuzé, Yingli Wang, Ethylin Wang Jabs, Kristina Aldridge, Joan T. Richtsmeier
I whakaputaina 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 mā Saskia C. Sanderson, Sabrina A. Suckiel, Micol Zweig, Erwin P. Böttinger, Ethylin Wang Jabs, Lynne D. Richardson
I whakaputaina 2015Artigo -
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Mapping the Treacher Collins syndrome locus to 5q31.3→q33.3 mā Ethylin Wang Jabs, Xiang Li, Cathleen A. Coss, Eugene W. Taylor, Deborah A. Meyers, James L. Weber
I whakaputaina 1991Artigo -
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The Ups and Downs of Mutation Frequencies during Aging Can Account for the Apert Syndrome Paternal Age Effect mā Song-Ro Yoon, Jian Qin, Rivka L. Glaser, Ethylin Wang Jabs, Nancy S. Wexler, Rebecca Z. Sokol, Norman Arnheim, Peter Calabrese
I whakaputaina 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 mā Carol A. Wise, Lydia C. Chiang, William A. Paznekas, Mridula Sharma, Maurice M. Musy, Jennifer Ashley, Michael Lovett, Ethylin Wang Jabs
I whakaputaina 1997Artigo -
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Advancing age has differential effects on DNA damage, chromatin integrity, gene mutations, and aneuploidies in sperm mā Andrew J. Wyrobek, Brenda Eskenazi, Suzanne Young, Norman Arnheim, Irene Tiemann‐Boege, Ethylin Wang Jabs, Rivka L. Glaser, Francesca Pearson, D.P. Evenson
I whakaputaina 2006Artigo
Ngā utauta rapu:
Ngā marau whai pānga
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