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J G Davis

Showing results (81-90 of 97) with videos related to

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Journal of Pediatric Orthopedics|November 30, 2000
The incidence of protrusio acetabuli in Marfan's syndrome and its relationship to bone mineral densityT Do, P F Giampietro, S W Burke, et al.
Oncogene|July 22, 1998
Absence of autophosphorylation site Y882 in the p185neu oncogene product correlates with a reduction of transforming potentialH T Zhang, D M O'Rourke, H Zhao, et al.
Developmental Medicine and Child Neurology|December 1, 1992
Fanconi anemia: a model for genetic causes of abnormal brain developmentS G Pavlakis, C L Frissora, P F Giampietro, et al.
Cell|July 28, 1989
Synergistic interaction of p185c-neu and the EGF receptor leads to transformation of rodent fibroblastsY Kokai, J N Myers, T Wada, et al.
Cytogenetics and Cell Genetics|January 1, 1997
Definition of the critical interval for Smith-Magenis syndromeS H Elsea, S M Purandare, R A Adell, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 21, 2001
Insurance reimbursement for risk-reducing mastectomy and oophorectomy in women with BRCA1 or BRCA2 mutationsN D Kauff, L Scheuer, M E Robson, et al.
The American Journal of Cardiology|May 11, 1999
Phenotypic features and impact of beta blocker or calcium antagonist therapy on aortic lumen size in the Marfan syndromeR Rossi-Foulkes, M J Roman, S E Rosen, et al.
Bone Marrow Transplantation|March 30, 2001
Peripheral blood progenitor cell mobilisation alters myeloid, but not erythroid, progenitor cell self-renewal kineticsS B Marley, J L Lewis, B Zheng, et al.
Oncogene|April 7, 1998
Inhibition of a naturally occurring EGFR oncoprotein by the p185neu ectodomain: implications for subdomain contributions to receptor assemblyD M O'Rourke, E J Nute, J G Davis, et al.
Biochemical and Molecular Medicine|October 1, 1995
Substitution of alanine543 with a threonine residue at the carboxy terminal end of the beta-chain is associated with thermolabile hexosaminidase B in a Jewish family of Oriental ancestryR De Gasperi, M A Gama Sosa, E E Grebner, et al.
Pageof 10

Showing results (81-90 of 97) with videos related to

Sort By:
Pageof 10
Journal of Pediatric Orthopedics|November 30, 2000
The incidence of protrusio acetabuli in Marfan's syndrome and its relationship to bone mineral densityT Do, P F Giampietro, S W Burke, et al.
Oncogene|July 22, 1998
Absence of autophosphorylation site Y882 in the p185neu oncogene product correlates with a reduction of transforming potentialH T Zhang, D M O'Rourke, H Zhao, et al.
Developmental Medicine and Child Neurology|December 1, 1992
Fanconi anemia: a model for genetic causes of abnormal brain developmentS G Pavlakis, C L Frissora, P F Giampietro, et al.
Cell|July 28, 1989
Synergistic interaction of p185c-neu and the EGF receptor leads to transformation of rodent fibroblastsY Kokai, J N Myers, T Wada, et al.
Cytogenetics and Cell Genetics|January 1, 1997
Definition of the critical interval for Smith-Magenis syndromeS H Elsea, S M Purandare, R A Adell, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 21, 2001
Insurance reimbursement for risk-reducing mastectomy and oophorectomy in women with BRCA1 or BRCA2 mutationsN D Kauff, L Scheuer, M E Robson, et al.
The American Journal of Cardiology|May 11, 1999
Phenotypic features and impact of beta blocker or calcium antagonist therapy on aortic lumen size in the Marfan syndromeR Rossi-Foulkes, M J Roman, S E Rosen, et al.
Bone Marrow Transplantation|March 30, 2001
Peripheral blood progenitor cell mobilisation alters myeloid, but not erythroid, progenitor cell self-renewal kineticsS B Marley, J L Lewis, B Zheng, et al.
Oncogene|April 7, 1998
Inhibition of a naturally occurring EGFR oncoprotein by the p185neu ectodomain: implications for subdomain contributions to receptor assemblyD M O'Rourke, E J Nute, J G Davis, et al.
Biochemical and Molecular Medicine|October 1, 1995
Substitution of alanine543 with a threonine residue at the carboxy terminal end of the beta-chain is associated with thermolabile hexosaminidase B in a Jewish family of Oriental ancestryR De Gasperi, M A Gama Sosa, E E Grebner, et al.
Pageof 10