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D A Marchuk

Showing results (31-40 of 70) with videos related to

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Genomics|August 1, 1992
NF1-related locus on chromosome 15E Legius, D A Marchuk, B K Hall, et al.
Kidney International|September 14, 2007
Hypertension and albuminuria in chronic kidney disease mapped to a mouse chromosome 11 locusH R Salzler, R Griffiths, P Ruiz, et al.
Blood|December 9, 1998
Cloning of the promoter region of human endoglin, the target gene for hereditary hemorrhagic telangiectasia type 1C Ríus, J D Smith, N Almendro, et al.
Orphanet Journal of Rare Diseases|September 20, 2021
Utility of modified Rankin Scale for brain vascular malformations in hereditary hemorrhagic telangiectasiaK P Thompson, J Nelson, H Kim, et al.
Human Mutation|March 1, 2000
Novel missense and frameshift mutations in the activin receptor-like kinase-1 gene in hereditary hemorrhagic telangiectasia. Mutations in brief no. 164. OnlineD J Klaus, C J Gallione, K Anthony, et al.
Angiogenesis|May 31, 2022
A novel somatic mutation in GNAQ in a capillary malformation provides insight into molecular pathogenesisF Galeffi, D A Snellings, S E Wetzel-Strong, et al.
DNA Sequence : the Journal of DNA Sequencing and Mapping|January 1, 1992
Sequencing and analysis of genomic fragments from the NF1 locusA Martin-Gallardo, D A Marchuk, J Gocayne, et al.
Neurosurgery|October 3, 2000
Abnormal pattern of Tie-2 and vascular endothelial growth factor receptor expression in human cerebral arteriovenous malformationsT Hashimoto, C W Emala, S Joshi, et al.
The European Respiratory Journal|April 7, 2004
Primary pulmonary hypertension in families with hereditary haemorrhagic telangiectasiaS A Abdalla, C J Gallione, R J Barst, et al.
Genomics|February 10, 1995
COL5A1: fine genetic mapping and exclusion as candidate gene in families with nail-patella syndrome, tuberous sclerosis 1, hereditary hemorrhagic telangiectasia, and Ehlers-Danlos Syndrome type IID S Greenspan, H Northrup, K S Au, et al.
Pageof 7

Showing results (31-40 of 70) with videos related to

Sort By:
Pageof 7
Genomics|August 1, 1992
NF1-related locus on chromosome 15E Legius, D A Marchuk, B K Hall, et al.
Kidney International|September 14, 2007
Hypertension and albuminuria in chronic kidney disease mapped to a mouse chromosome 11 locusH R Salzler, R Griffiths, P Ruiz, et al.
Blood|December 9, 1998
Cloning of the promoter region of human endoglin, the target gene for hereditary hemorrhagic telangiectasia type 1C Ríus, J D Smith, N Almendro, et al.
Orphanet Journal of Rare Diseases|September 20, 2021
Utility of modified Rankin Scale for brain vascular malformations in hereditary hemorrhagic telangiectasiaK P Thompson, J Nelson, H Kim, et al.
Human Mutation|March 1, 2000
Novel missense and frameshift mutations in the activin receptor-like kinase-1 gene in hereditary hemorrhagic telangiectasia. Mutations in brief no. 164. OnlineD J Klaus, C J Gallione, K Anthony, et al.
Angiogenesis|May 31, 2022
A novel somatic mutation in GNAQ in a capillary malformation provides insight into molecular pathogenesisF Galeffi, D A Snellings, S E Wetzel-Strong, et al.
DNA Sequence : the Journal of DNA Sequencing and Mapping|January 1, 1992
Sequencing and analysis of genomic fragments from the NF1 locusA Martin-Gallardo, D A Marchuk, J Gocayne, et al.
Neurosurgery|October 3, 2000
Abnormal pattern of Tie-2 and vascular endothelial growth factor receptor expression in human cerebral arteriovenous malformationsT Hashimoto, C W Emala, S Joshi, et al.
The European Respiratory Journal|April 7, 2004
Primary pulmonary hypertension in families with hereditary haemorrhagic telangiectasiaS A Abdalla, C J Gallione, R J Barst, et al.
Genomics|February 10, 1995
COL5A1: fine genetic mapping and exclusion as candidate gene in families with nail-patella syndrome, tuberous sclerosis 1, hereditary hemorrhagic telangiectasia, and Ehlers-Danlos Syndrome type IID S Greenspan, H Northrup, K S Au, et al.
Pageof 7