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Showing results (121-130 of 129) with videos related to

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Developmental Biology|July 10, 1996
A candidate gene for the amnionless gastrulation stage mouse mutation encodes a TRAF-related proteinX Wang, E A Bornslaeger, O Haub, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1991
Cloning and primary structure of a human islet isoform of glutamic acid decarboxylase from chromosome 10A E Karlsen, W A Hagopian, C E Grubin, et al.
Science (New York, N.Y.)|February 12, 1993
CD40 ligand gene defects responsible for X-linked hyper-IgM syndromeR C Allen, R J Armitage, M E Conley, et al.
Human Molecular Genetics|October 1, 1996
cDNA cloning and chromosome mapping of the human Fe65 gene: interaction of the conserved cytoplasmic domains of the human beta-amyloid precursor protein and its homologues with the mouse Fe65 proteinS L Bressler, M D Gray, B L Sopher, et al.
Human Molecular Genetics|December 1, 1996
Human huntingtin derived from YAC transgenes compensates for loss of murine huntingtin by rescue of the embryonic lethal phenotypeJ G Hodgson, D J Smith, K McCutcheon, et al.
Circulation Research|September 1, 1996
Cloning and characterization of rat density-enhanced phosphatase-1, a protein tyrosine phosphatase expressed by vascular cellsL G Borges, R A Seifert, F J Grant, et al.
Human Molecular Genetics|November 1, 1996
Recurrent duplication and deletion polymorphisms on the long arm of the Y chromosome in normal malesM A Jobling, V Samara, A Pandya, et al.
Human Molecular Genetics|April 18, 1998
The mouse Mid1 gene: implications for the pathogenesis of Opitz syndrome and the evolution of the mammalian pseudoautosomal regionL Dal Zotto, N A Quaderi, R Elliott, et al.
Prenatal Diagnosis|March 1, 1997
Rare trisomy mosaicism diagnosed in amniocytes, involving an autosome other than chromosomes 13, 18, 20, and 21: karyotype/phenotype correlationsL Y Hsu, M T Yu, R L Neu, et al.
Pageof 13

Showing results (121-130 of 129) with videos related to

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Pageof 13
You have reached the last page of results.This site can display upto 129 results.
Developmental Biology|July 10, 1996
A candidate gene for the amnionless gastrulation stage mouse mutation encodes a TRAF-related proteinX Wang, E A Bornslaeger, O Haub, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1991
Cloning and primary structure of a human islet isoform of glutamic acid decarboxylase from chromosome 10A E Karlsen, W A Hagopian, C E Grubin, et al.
Science (New York, N.Y.)|February 12, 1993
CD40 ligand gene defects responsible for X-linked hyper-IgM syndromeR C Allen, R J Armitage, M E Conley, et al.
Human Molecular Genetics|October 1, 1996
cDNA cloning and chromosome mapping of the human Fe65 gene: interaction of the conserved cytoplasmic domains of the human beta-amyloid precursor protein and its homologues with the mouse Fe65 proteinS L Bressler, M D Gray, B L Sopher, et al.
Human Molecular Genetics|December 1, 1996
Human huntingtin derived from YAC transgenes compensates for loss of murine huntingtin by rescue of the embryonic lethal phenotypeJ G Hodgson, D J Smith, K McCutcheon, et al.
Circulation Research|September 1, 1996
Cloning and characterization of rat density-enhanced phosphatase-1, a protein tyrosine phosphatase expressed by vascular cellsL G Borges, R A Seifert, F J Grant, et al.
Human Molecular Genetics|November 1, 1996
Recurrent duplication and deletion polymorphisms on the long arm of the Y chromosome in normal malesM A Jobling, V Samara, A Pandya, et al.
Human Molecular Genetics|April 18, 1998
The mouse Mid1 gene: implications for the pathogenesis of Opitz syndrome and the evolution of the mammalian pseudoautosomal regionL Dal Zotto, N A Quaderi, R Elliott, et al.
Prenatal Diagnosis|March 1, 1997
Rare trisomy mosaicism diagnosed in amniocytes, involving an autosome other than chromosomes 13, 18, 20, and 21: karyotype/phenotype correlationsL Y Hsu, M T Yu, R L Neu, et al.
Pageof 13