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Showing results (221-230 of 227) with videos related to

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European Journal of Human Genetics : EJHG|February 15, 2001
Elastin: mutational spectrum in supravalvular aortic stenosisK Metcalfe, A K Rucka, L Smoot, et al.
The Journal of Biological Chemistry|September 9, 2000
Serine 727 phosphorylation and activation of cytosolic phospholipase A2 by MNK1-related protein kinasesY Hefner, A G Borsch-Haubold, M Murakami, et al.
Journal of Proteomics|July 15, 2015
ProLuCID: An improved SEQUEST-like algorithm with enhanced sensitivity and specificityT Xu, S K Park, J D Venable, et al.
Genomics|May 8, 1998
Characterization of SCML1, a new gene in Xp22, with homology to developmental polycomb genesE van de Vosse, S M Walpole, A Nicolaou, et al.
Molecular Psychiatry|April 2, 2014
Phenotypic differences in hiPSC NPCs derived from patients with schizophreniaK Brennand, J N Savas, Y Kim, et al.
American Journal of Human Genetics|July 20, 2001
p63 Gene mutations in eec syndrome, limb-mammary syndrome, and isolated split hand-split foot malformation suggest a genotype-phenotype correlationH van Bokhoven, B C Hamel, M Bamshad, et al.
Science (New York, N.Y.)|August 8, 1997
Identification of the tuberous sclerosis gene TSC1 on chromosome 9q34M van Slegtenhorst, R de Hoogt, C Hermans, et al.
Pageof 23

Showing results (221-230 of 227) with videos related to

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Pageof 23
You have reached the last page of results.This site can display upto 227 results.
European Journal of Human Genetics : EJHG|February 15, 2001
Elastin: mutational spectrum in supravalvular aortic stenosisK Metcalfe, A K Rucka, L Smoot, et al.
The Journal of Biological Chemistry|September 9, 2000
Serine 727 phosphorylation and activation of cytosolic phospholipase A2 by MNK1-related protein kinasesY Hefner, A G Borsch-Haubold, M Murakami, et al.
Journal of Proteomics|July 15, 2015
ProLuCID: An improved SEQUEST-like algorithm with enhanced sensitivity and specificityT Xu, S K Park, J D Venable, et al.
Genomics|May 8, 1998
Characterization of SCML1, a new gene in Xp22, with homology to developmental polycomb genesE van de Vosse, S M Walpole, A Nicolaou, et al.
Molecular Psychiatry|April 2, 2014
Phenotypic differences in hiPSC NPCs derived from patients with schizophreniaK Brennand, J N Savas, Y Kim, et al.
American Journal of Human Genetics|July 20, 2001
p63 Gene mutations in eec syndrome, limb-mammary syndrome, and isolated split hand-split foot malformation suggest a genotype-phenotype correlationH van Bokhoven, B C Hamel, M Bamshad, et al.
Science (New York, N.Y.)|August 8, 1997
Identification of the tuberous sclerosis gene TSC1 on chromosome 9q34M van Slegtenhorst, R de Hoogt, C Hermans, et al.
Pageof 23