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Showing results (171-180 of 181) with videos related to

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Nouvelle Revue Francaise D'Hematologie|January 1, 1981
[Refractory anaemia with an excess of myeloblasts and cutaneous vasculitis (author's transl)]B Dreyfus, J P Vernant, J Wechsler, et al.
The British Journal of Dermatology|September 18, 2008
Cutaneous manifestations of immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndromeM Halabi-Tawil, F M Ruemmele, S Fraitag, et al.
American Journal of Human Genetics|August 27, 1998
Deletions within COL7A1 exons distant from consensus splice sites alter splicing and produce shortened polypeptides in dominant dystrophic epidermolysis bullosaA Sakuntabhai, N Hammami-Hauasli, C Bodemer, et al.
The Journal of Investigative Dermatology|April 1, 1995
DNA-based prenatal diagnosis of generalized recessive dystrophic epidermolysis bullosa in six pregnancies at risk for recurrenceA Hovnanian, L Hilal, C Blanchet-Bardon, et al.
The Journal of Investigative Dermatology|November 1, 1990
Reversal effects of topical retinoic acid on the skin of kidney transplant recipients under systemic corticotherapyO De Lacharriére, C Escoffier, A M Gracia, et al.
American Journal of Medical Genetics|October 26, 1999
Skin elastic fibers in Williams syndromeS M Dridi, S Ghomrasseni, D Bonnet, et al.
European Journal of Human Genetics : EJHG|July 1, 1997
Three novel point mutations in the keratinocyte transglutaminase (TGK) gene in lamellar ichthyosis: significance for mutant transcript level, TGK immunodetection and activityE Petit, M Huber, A Rochat, et al.
American Journal of Human Genetics|October 27, 1997
Characterization of 18 new mutations in COL7A1 in recessive dystrophic epidermolysis bullosa provides evidence for distinct molecular mechanisms underlying defective anchoring fibril formationA Hovnanian, A Rochat, C Bodemer, et al.
Nature Genetics|June 3, 2000
Mutations in SPINK5, encoding a serine protease inhibitor, cause Netherton syndromeS Chavanas, C Bodemer, A Rochat, et al.
The British Journal of Dermatology|April 16, 2003
International Consensus Conference on Atopic Dermatitis II (ICCAD II): clinical update and current treatment strategiesC Ellis, T Luger, D Abeck, et al.
Pageof 19

Showing results (171-180 of 181) with videos related to

Sort By:
Pageof 19
Nouvelle Revue Francaise D'Hematologie|January 1, 1981
[Refractory anaemia with an excess of myeloblasts and cutaneous vasculitis (author's transl)]B Dreyfus, J P Vernant, J Wechsler, et al.
The British Journal of Dermatology|September 18, 2008
Cutaneous manifestations of immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndromeM Halabi-Tawil, F M Ruemmele, S Fraitag, et al.
American Journal of Human Genetics|August 27, 1998
Deletions within COL7A1 exons distant from consensus splice sites alter splicing and produce shortened polypeptides in dominant dystrophic epidermolysis bullosaA Sakuntabhai, N Hammami-Hauasli, C Bodemer, et al.
The Journal of Investigative Dermatology|April 1, 1995
DNA-based prenatal diagnosis of generalized recessive dystrophic epidermolysis bullosa in six pregnancies at risk for recurrenceA Hovnanian, L Hilal, C Blanchet-Bardon, et al.
The Journal of Investigative Dermatology|November 1, 1990
Reversal effects of topical retinoic acid on the skin of kidney transplant recipients under systemic corticotherapyO De Lacharriére, C Escoffier, A M Gracia, et al.
American Journal of Medical Genetics|October 26, 1999
Skin elastic fibers in Williams syndromeS M Dridi, S Ghomrasseni, D Bonnet, et al.
European Journal of Human Genetics : EJHG|July 1, 1997
Three novel point mutations in the keratinocyte transglutaminase (TGK) gene in lamellar ichthyosis: significance for mutant transcript level, TGK immunodetection and activityE Petit, M Huber, A Rochat, et al.
American Journal of Human Genetics|October 27, 1997
Characterization of 18 new mutations in COL7A1 in recessive dystrophic epidermolysis bullosa provides evidence for distinct molecular mechanisms underlying defective anchoring fibril formationA Hovnanian, A Rochat, C Bodemer, et al.
Nature Genetics|June 3, 2000
Mutations in SPINK5, encoding a serine protease inhibitor, cause Netherton syndromeS Chavanas, C Bodemer, A Rochat, et al.
The British Journal of Dermatology|April 16, 2003
International Consensus Conference on Atopic Dermatitis II (ICCAD II): clinical update and current treatment strategiesC Ellis, T Luger, D Abeck, et al.
Pageof 19