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J M Derry

Showing results (11-20 of 19) with videos related to

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Cell|March 8, 1996
Wiskott-Aldrich syndrome protein, a novel effector for the GTPase CDC42Hs, is implicated in actin polymerizationM Symons, J M Derry, B Karlak, et al.
Human Molecular Genetics|October 1, 1992
Expression of four alternative dystrophin transcripts in brain regions regulated by different promotersD C Górecki, A P Monaco, J M Derry, et al.
Nature Genetics|July 3, 1999
Mutations in a delta 8-delta 7 sterol isomerase in the tattered mouse and X-linked dominant chondrodysplasia punctata. jderry@immunex.comJ M Derry, E Gormally, G D Means, et al.
Blood|November 15, 1995
The Wiskott-Aldrich syndrome and X-linked congenital thrombocytopenia are caused by mutations of the same geneQ Zhu, M Zhang, R M Blaese, et al.
Human Molecular Genetics|July 1, 1995
WASP gene mutations in Wiskott-Aldrich syndrome and X-linked thrombocytopeniaJ M Derry, J A Kerns, K I Weinberg, et al.
Genomics|September 20, 1995
The mouse homolog of the Wiskott-Aldrich syndrome protein (WASP) gene is highly conserved and maps near the scurfy (sf) mutation on the X chromosomeJ M Derry, P Wiedemann, P Blair, et al.
Cytokine|February 7, 1998
Molecular characterization of the human interleukin (IL)-17 receptorZ Yao, M K Spriggs, J M Derry, et al.
Gene Therapy|March 1, 2000
Expression of human Wiskott-Aldrich syndrome protein in patients' cells leads to partial correction of a phenotypic abnormality of cell surface glycoproteinsM M Huang, S Tsuboi, A Wong, et al.
Neuron|November 1, 1989
Chromosomal localization of GABAA receptor subunit genes: relationship to human genetic diseaseV J Buckle, N Fujita, A S Ryder-Cook, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Cell|March 8, 1996
Wiskott-Aldrich syndrome protein, a novel effector for the GTPase CDC42Hs, is implicated in actin polymerizationM Symons, J M Derry, B Karlak, et al.
Human Molecular Genetics|October 1, 1992
Expression of four alternative dystrophin transcripts in brain regions regulated by different promotersD C Górecki, A P Monaco, J M Derry, et al.
Nature Genetics|July 3, 1999
Mutations in a delta 8-delta 7 sterol isomerase in the tattered mouse and X-linked dominant chondrodysplasia punctata. jderry@immunex.comJ M Derry, E Gormally, G D Means, et al.
Blood|November 15, 1995
The Wiskott-Aldrich syndrome and X-linked congenital thrombocytopenia are caused by mutations of the same geneQ Zhu, M Zhang, R M Blaese, et al.
Human Molecular Genetics|July 1, 1995
WASP gene mutations in Wiskott-Aldrich syndrome and X-linked thrombocytopeniaJ M Derry, J A Kerns, K I Weinberg, et al.
Genomics|September 20, 1995
The mouse homolog of the Wiskott-Aldrich syndrome protein (WASP) gene is highly conserved and maps near the scurfy (sf) mutation on the X chromosomeJ M Derry, P Wiedemann, P Blair, et al.
Cytokine|February 7, 1998
Molecular characterization of the human interleukin (IL)-17 receptorZ Yao, M K Spriggs, J M Derry, et al.
Gene Therapy|March 1, 2000
Expression of human Wiskott-Aldrich syndrome protein in patients' cells leads to partial correction of a phenotypic abnormality of cell surface glycoproteinsM M Huang, S Tsuboi, A Wong, et al.
Neuron|November 1, 1989
Chromosomal localization of GABAA receptor subunit genes: relationship to human genetic diseaseV J Buckle, N Fujita, A S Ryder-Cook, et al.
Pageof 2