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D A Marchuk

Showing results (61-70 of 70) with videos related to

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Cell|December 27, 1996
Vascular dysmorphogenesis caused by an activating mutation in the receptor tyrosine kinase TIE2M Vikkula, L M Boon, K L Carraway, et al.
Journal of Medical Genetics|April 15, 2006
SMAD4 mutations found in unselected HHT patientsC J Gallione, J A Richards, T G W Letteboer, et al.
American Journal of Human Genetics|April 20, 2001
Identification and expression analysis of spastin gene mutations in hereditary spastic paraplegiaI K Svenson, A E Ashley-Koch, P C Gaskell, et al.
Human Molecular Genetics|June 17, 1999
Allelic and locus heterogeneity in inherited venous malformationsJ T Calvert, T J Riney, C D Kontos, et al.
Psychosomatic Medicine|April 9, 2001
Central nervous system serotonin function and cardiovascular responses to stressR B Williams, D A Marchuk, K M Gadde, et al.
Neurogenetics|May 17, 2001
Fine mapping and genetic heterogeneity in the pure form of autosomal dominant familial spastic paraplegiaA Ashley-Koch, E R Bonner, P C Gaskell, et al.
Nature Genetics|June 1, 1996
Mutations in the activin receptor-like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2D W Johnson, J N Berg, M A Baldwin, et al.
Genome Research|November 1, 1995
Refined localization of the cerebral cavernous malformation gene (CCM1) to a 4-cM interval of chromosome 7q contained in a well-defined YAC contigE W Johnson, L M Iyer, S S Rich, et al.
Human Mutation|April 29, 1998
Mutation and expression analysis of the endoglin gene in hereditary hemorrhagic telangiectasia reveals null allelesC J Gallione, D J Klaus, E Y Yeh, et al.
Human Molecular Genetics|November 5, 1999
Mutations in the gene encoding KRIT1, a Krev-1/rap1a binding protein, cause cerebral cavernous malformations (CCM1)T Sahoo, E W Johnson, J W Thomas, et al.
Pageof 7

Showing results (61-70 of 70) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 70 results.
Cell|December 27, 1996
Vascular dysmorphogenesis caused by an activating mutation in the receptor tyrosine kinase TIE2M Vikkula, L M Boon, K L Carraway, et al.
Journal of Medical Genetics|April 15, 2006
SMAD4 mutations found in unselected HHT patientsC J Gallione, J A Richards, T G W Letteboer, et al.
American Journal of Human Genetics|April 20, 2001
Identification and expression analysis of spastin gene mutations in hereditary spastic paraplegiaI K Svenson, A E Ashley-Koch, P C Gaskell, et al.
Human Molecular Genetics|June 17, 1999
Allelic and locus heterogeneity in inherited venous malformationsJ T Calvert, T J Riney, C D Kontos, et al.
Psychosomatic Medicine|April 9, 2001
Central nervous system serotonin function and cardiovascular responses to stressR B Williams, D A Marchuk, K M Gadde, et al.
Neurogenetics|May 17, 2001
Fine mapping and genetic heterogeneity in the pure form of autosomal dominant familial spastic paraplegiaA Ashley-Koch, E R Bonner, P C Gaskell, et al.
Nature Genetics|June 1, 1996
Mutations in the activin receptor-like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2D W Johnson, J N Berg, M A Baldwin, et al.
Genome Research|November 1, 1995
Refined localization of the cerebral cavernous malformation gene (CCM1) to a 4-cM interval of chromosome 7q contained in a well-defined YAC contigE W Johnson, L M Iyer, S S Rich, et al.
Human Mutation|April 29, 1998
Mutation and expression analysis of the endoglin gene in hereditary hemorrhagic telangiectasia reveals null allelesC J Gallione, D J Klaus, E Y Yeh, et al.
Human Molecular Genetics|November 5, 1999
Mutations in the gene encoding KRIT1, a Krev-1/rap1a binding protein, cause cerebral cavernous malformations (CCM1)T Sahoo, E W Johnson, J W Thomas, et al.
Pageof 7