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M Peacocke

Showing results (31-40 of 56) with videos related to

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Experimental Cell Research|December 15, 1996
Age-associated changes in basal c-fos transcription factor binding activity in rat heartsH Tsou, G Azhar, X G Lu, et al.
Experimental Cell Research|November 26, 1998
Repression of transactivation of the retinoic acid receptor beta2 promoter in human breast cancer cellsH C Tsou, Y J Yao, X X Xie, et al.
Journal of Investigative Medicine : the Official Publication of the American Federation for Clinical Research|April 1, 1995
A diagnostic assay for the Wiskott-Aldrich syndrome and its variant formsK A Siminovitch, W L Greer, A Novogrodsky, et al.
Experimental Cell Research|November 21, 1997
Expression of retinoid X receptors in human dermal fibroblastsH C Tsou, X X Xie, Y J Yao, et al.
Immunodeficiency|January 1, 1993
Selective impairment of CD43-mediated T cell activation in the Wiskott-Aldrich syndromeK A Siminovitch, W L Greer, B Axelsson, et al.
American Journal of Medical Genetics|March 2, 1999
Severe Lhermitte-Duclos disease with unique germline mutation of PTENR Sutphen, T M Diamond, S E Minton, et al.
Experimental Dermatology|May 8, 1999
Identification of PTEN mutations in five families with Bannayan-Zonana syndromeJ Tok Celebi, F F Chen, H Zhang, et al.
Genomics|March 1, 1990
Linkage relationships of the Wiskott-Aldrich syndrome to 10 loci in the pericentromeric region of the human X chromosomeW L Greer, A K Somani, P C Kwong, et al.
Human Genetics|October 1, 1993
Linkage of Wiskott-Aldrich syndrome with three marker loci, DXS426, SYP and TFE3, which map to the Xp11.3-p11.22 regionS M Cremin, W L Greer, R Bodok-Nutzati, et al.
Genomics|January 1, 1989
X-chromosome inactivation in the Wiskott-Aldrich syndrome: a marker for detection of the carrier state and identification of cell lineages expressing the gene defectW L Greer, P C Kwong, M Peacocke, et al.
Pageof 6

Showing results (31-40 of 56) with videos related to

Sort By:
Pageof 6
Experimental Cell Research|December 15, 1996
Age-associated changes in basal c-fos transcription factor binding activity in rat heartsH Tsou, G Azhar, X G Lu, et al.
Experimental Cell Research|November 26, 1998
Repression of transactivation of the retinoic acid receptor beta2 promoter in human breast cancer cellsH C Tsou, Y J Yao, X X Xie, et al.
Journal of Investigative Medicine : the Official Publication of the American Federation for Clinical Research|April 1, 1995
A diagnostic assay for the Wiskott-Aldrich syndrome and its variant formsK A Siminovitch, W L Greer, A Novogrodsky, et al.
Experimental Cell Research|November 21, 1997
Expression of retinoid X receptors in human dermal fibroblastsH C Tsou, X X Xie, Y J Yao, et al.
Immunodeficiency|January 1, 1993
Selective impairment of CD43-mediated T cell activation in the Wiskott-Aldrich syndromeK A Siminovitch, W L Greer, B Axelsson, et al.
American Journal of Medical Genetics|March 2, 1999
Severe Lhermitte-Duclos disease with unique germline mutation of PTENR Sutphen, T M Diamond, S E Minton, et al.
Experimental Dermatology|May 8, 1999
Identification of PTEN mutations in five families with Bannayan-Zonana syndromeJ Tok Celebi, F F Chen, H Zhang, et al.
Genomics|March 1, 1990
Linkage relationships of the Wiskott-Aldrich syndrome to 10 loci in the pericentromeric region of the human X chromosomeW L Greer, A K Somani, P C Kwong, et al.
Human Genetics|October 1, 1993
Linkage of Wiskott-Aldrich syndrome with three marker loci, DXS426, SYP and TFE3, which map to the Xp11.3-p11.22 regionS M Cremin, W L Greer, R Bodok-Nutzati, et al.
Genomics|January 1, 1989
X-chromosome inactivation in the Wiskott-Aldrich syndrome: a marker for detection of the carrier state and identification of cell lineages expressing the gene defectW L Greer, P C Kwong, M Peacocke, et al.
Pageof 6