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W C Nichols

Showing results (71-80 of 78) with videos related to

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Nature Genetics|March 1, 1997
Localization of the gene for familial primary pulmonary hypertension to chromosome 2q31-32W C Nichols, D L Koller, B Slovis, et al.
The New England Journal of Medicine|August 4, 2001
Clinical and molecular genetic features of pulmonary hypertension in patients with hereditary hemorrhagic telangiectasiaR C Trembath, J R Thomson, R D Machado, et al.
Nature|October 5, 2001
Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpuraG G Levy, W C Nichols, E C Lian, et al.
Blood|March 26, 1999
ERGIC-53 gene structure and mutation analysis in 19 combined factors V and VIII deficiency familiesW C Nichols, V H Terry, M A Wheatley, et al.
Neurobiology of Disease|January 26, 2018
Alpha galactosidase A activity in Parkinson's diseaseR N Alcalay, P Wolf, O A Levy, et al.
Journal of Medical Genetics|October 4, 2000
Sporadic primary pulmonary hypertension is associated with germline mutations of the gene encoding BMPR-II, a receptor member of the TGF-beta familyJ R Thomson, R D Machado, M W Pauciulo, et al.
American Journal of Human Genetics|December 15, 2000
BMPR2 haploinsufficiency as the inherited molecular mechanism for primary pulmonary hypertensionR D Machado, M W Pauciulo, J R Thomson, et al.
Neurology|March 14, 2008
Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson diseaseK Haugarvoll, R Rademakers, J M Kachergus, et al.
Pageof 8

Showing results (71-80 of 78) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 78 results.
Nature Genetics|March 1, 1997
Localization of the gene for familial primary pulmonary hypertension to chromosome 2q31-32W C Nichols, D L Koller, B Slovis, et al.
The New England Journal of Medicine|August 4, 2001
Clinical and molecular genetic features of pulmonary hypertension in patients with hereditary hemorrhagic telangiectasiaR C Trembath, J R Thomson, R D Machado, et al.
Nature|October 5, 2001
Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpuraG G Levy, W C Nichols, E C Lian, et al.
Blood|March 26, 1999
ERGIC-53 gene structure and mutation analysis in 19 combined factors V and VIII deficiency familiesW C Nichols, V H Terry, M A Wheatley, et al.
Neurobiology of Disease|January 26, 2018
Alpha galactosidase A activity in Parkinson's diseaseR N Alcalay, P Wolf, O A Levy, et al.
Journal of Medical Genetics|October 4, 2000
Sporadic primary pulmonary hypertension is associated with germline mutations of the gene encoding BMPR-II, a receptor member of the TGF-beta familyJ R Thomson, R D Machado, M W Pauciulo, et al.
American Journal of Human Genetics|December 15, 2000
BMPR2 haploinsufficiency as the inherited molecular mechanism for primary pulmonary hypertensionR D Machado, M W Pauciulo, J R Thomson, et al.
Neurology|March 14, 2008
Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson diseaseK Haugarvoll, R Rademakers, J M Kachergus, et al.
Pageof 8