Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

D A Marchuk

Showing results (41-50 of 70) with videos related to

Pageof 7
Sort By:
Nucleic Acids Research|January 11, 1991
A polymorphic cDNA probe on chromosome 17q11.2 located within the NF1 gene [D17S376]L B Andersen, M R Wallace, D A Marchuk, et al.
Neuroscience|July 18, 2008
ZPLD1 gene is disrupted in a patient with balanced translocation that exhibits cerebral cavernous malformationsF Gianfrancesco, T Esposito, S Penco, et al.
Molecular and Cellular Biology|January 1, 1993
A conserved alternative splice in the von Recklinghausen neurofibromatosis (NF1) gene produces two neurofibromin isoforms, both of which have GTPase-activating protein activityL B Andersen, R Ballester, D A Marchuk, et al.
Journal of Clinical Pathology|March 17, 2001
Evidence for loss of heterozygosity of 5q in sporadic haemangiomas: are somatic mutations involved in haemangioma formation?J N Berg, J W Walter, U Thisanagayam, et al.
Journal of Medical Genetics|December 1, 1990
A 90 kb DNA deletion associated with neurofibromatosis type 1M Upadhyaya, A Cheryson, W Broadhead, et al.
Genes, Chromosomes & Cancer|November 1, 1990
A chromosome jump crosses a translocation breakpoint in the von Recklinghausen neurofibromatosis regionM R Wallace, L B Andersen, J W Fountain, et al.
Human Molecular Genetics|October 1, 1995
Six novel mutations in the endoglin gene in hereditary hemorrhagic telangiectasia type 1 suggest a dominant-negative effect of receptor functionK A McAllister, M A Baldwin, A K Thukkani, et al.
Annals of Neurology|May 1, 1997
Endoglin gene polymorphism as a risk factor for sporadic intracerebral hemorrhageM J Alberts, J P Davis, C Graffagnino, et al.
Genomics|March 1, 1991
cDNA sequence and genomic structure of EV12B, a gene lying within an intron of the neurofibromatosis type 1 geneR M Cawthon, L B Andersen, A M Buchberg, et al.
Genomics|December 1, 1991
cDNA cloning of the type 1 neurofibromatosis gene: complete sequence of the NF1 gene productD A Marchuk, A M Saulino, R Tavakkol, et al.
Pageof 7

Showing results (41-50 of 70) with videos related to

Sort By:
Pageof 7
Nucleic Acids Research|January 11, 1991
A polymorphic cDNA probe on chromosome 17q11.2 located within the NF1 gene [D17S376]L B Andersen, M R Wallace, D A Marchuk, et al.
Neuroscience|July 18, 2008
ZPLD1 gene is disrupted in a patient with balanced translocation that exhibits cerebral cavernous malformationsF Gianfrancesco, T Esposito, S Penco, et al.
Molecular and Cellular Biology|January 1, 1993
A conserved alternative splice in the von Recklinghausen neurofibromatosis (NF1) gene produces two neurofibromin isoforms, both of which have GTPase-activating protein activityL B Andersen, R Ballester, D A Marchuk, et al.
Journal of Clinical Pathology|March 17, 2001
Evidence for loss of heterozygosity of 5q in sporadic haemangiomas: are somatic mutations involved in haemangioma formation?J N Berg, J W Walter, U Thisanagayam, et al.
Journal of Medical Genetics|December 1, 1990
A 90 kb DNA deletion associated with neurofibromatosis type 1M Upadhyaya, A Cheryson, W Broadhead, et al.
Genes, Chromosomes & Cancer|November 1, 1990
A chromosome jump crosses a translocation breakpoint in the von Recklinghausen neurofibromatosis regionM R Wallace, L B Andersen, J W Fountain, et al.
Human Molecular Genetics|October 1, 1995
Six novel mutations in the endoglin gene in hereditary hemorrhagic telangiectasia type 1 suggest a dominant-negative effect of receptor functionK A McAllister, M A Baldwin, A K Thukkani, et al.
Annals of Neurology|May 1, 1997
Endoglin gene polymorphism as a risk factor for sporadic intracerebral hemorrhageM J Alberts, J P Davis, C Graffagnino, et al.
Genomics|March 1, 1991
cDNA sequence and genomic structure of EV12B, a gene lying within an intron of the neurofibromatosis type 1 geneR M Cawthon, L B Andersen, A M Buchberg, et al.
Genomics|December 1, 1991
cDNA cloning of the type 1 neurofibromatosis gene: complete sequence of the NF1 gene productD A Marchuk, A M Saulino, R Tavakkol, et al.
Pageof 7