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S Kenwrick

Showing results (51-60 of 57) with videos related to

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Human Molecular Genetics|October 9, 2001
A recurrent deletion in the ubiquitously expressed NEMO (IKK-gamma) gene accounts for the vast majority of incontinentia pigmenti mutationsS Aradhya, H Woffendin, T Jakins, et al.
American Journal of Medical Genetics|April 11, 2000
Human homologue of the murine bare patches/striated gene is not mutated in incontinentia pigmenti type 2S Aradhya, D L Nelson, N S Heiss, et al.
Journal of Medical Genetics|January 15, 2000
Mutation analysis of the DKC1 gene in incontinentia pigmentiN S Heiss, A Poustka, S W Knight, et al.
American Journal of Medical Genetics|September 12, 2000
Filamin (FLN1), plexin (SEX), major palmitoylated protein p55 (MPP1), and von-Hippel Lindau binding protein (VBP1) are not involved in incontinentia pigmenti type 2S Aradhya, P Ahobila, R A Lewis, et al.
Human Mutation|January 1, 1997
Nine novel L1 CAM mutations in families with X-linked hydrocephalusJ R MacFarlane, J S Du, M E Pepys, et al.
American Journal of Human Genetics|October 24, 2001
Survival of male patients with incontinentia pigmenti carrying a lethal mutation can be explained by somatic mosaicism or Klinefelter syndromeS Kenwrick, H Woffendin, T Jakins, et al.
Nature Genetics|March 10, 2001
X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-kappaB signalingR Döffinger, A Smahi, C Bessia, et al.
Pageof 6

Showing results (51-60 of 57) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 57 results.
Human Molecular Genetics|October 9, 2001
A recurrent deletion in the ubiquitously expressed NEMO (IKK-gamma) gene accounts for the vast majority of incontinentia pigmenti mutationsS Aradhya, H Woffendin, T Jakins, et al.
American Journal of Medical Genetics|April 11, 2000
Human homologue of the murine bare patches/striated gene is not mutated in incontinentia pigmenti type 2S Aradhya, D L Nelson, N S Heiss, et al.
Journal of Medical Genetics|January 15, 2000
Mutation analysis of the DKC1 gene in incontinentia pigmentiN S Heiss, A Poustka, S W Knight, et al.
American Journal of Medical Genetics|September 12, 2000
Filamin (FLN1), plexin (SEX), major palmitoylated protein p55 (MPP1), and von-Hippel Lindau binding protein (VBP1) are not involved in incontinentia pigmenti type 2S Aradhya, P Ahobila, R A Lewis, et al.
Human Mutation|January 1, 1997
Nine novel L1 CAM mutations in families with X-linked hydrocephalusJ R MacFarlane, J S Du, M E Pepys, et al.
American Journal of Human Genetics|October 24, 2001
Survival of male patients with incontinentia pigmenti carrying a lethal mutation can be explained by somatic mosaicism or Klinefelter syndromeS Kenwrick, H Woffendin, T Jakins, et al.
Nature Genetics|March 10, 2001
X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-kappaB signalingR Döffinger, A Smahi, C Bessia, et al.
Pageof 6