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Cell
|
March 8, 1996
Wiskott-Aldrich syndrome protein, a novel effector for the GTPase CDC42Hs, is implicated in actin polymerization
M 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 promoters
D 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.com
J 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 gene
Q Zhu, M Zhang, R M Blaese, et al.
Human Molecular Genetics
|
July 1, 1995
WASP gene mutations in Wiskott-Aldrich syndrome and X-linked thrombocytopenia
J 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 chromosome
J M Derry, P Wiedemann, P Blair, et al.
Cytokine
|
February 7, 1998
Molecular characterization of the human interleukin (IL)-17 receptor
Z 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 glycoproteins
M M Huang, S Tsuboi, A Wong, et al.
Neuron
|
November 1, 1989
Chromosomal localization of GABAA receptor subunit genes: relationship to human genetic disease
V J Buckle, N Fujita, A S Ryder-Cook, et al.
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of 2
Search research articles
Search
Showing results (11-20 of 19) with videos related to
Sort By:
Page
of 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 polymerization
M 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 promoters
D 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.com
J 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 gene
Q Zhu, M Zhang, R M Blaese, et al.
Human Molecular Genetics
|
July 1, 1995
WASP gene mutations in Wiskott-Aldrich syndrome and X-linked thrombocytopenia
J 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 chromosome
J M Derry, P Wiedemann, P Blair, et al.
Cytokine
|
February 7, 1998
Molecular characterization of the human interleukin (IL)-17 receptor
Z 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 glycoproteins
M M Huang, S Tsuboi, A Wong, et al.
Neuron
|
November 1, 1989
Chromosomal localization of GABAA receptor subunit genes: relationship to human genetic disease
V J Buckle, N Fujita, A S Ryder-Cook, et al.
Page
of 2