Search research articles
Contact Us
Filters
Showing results (81-90 of 97) with videos related to
Page
of 10
Sort By:
Journal of Pediatric Orthopedics
|
November 30, 2000
The incidence of protrusio acetabuli in Marfan's syndrome and its relationship to bone mineral density
T 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 potential
H 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 development
S 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 fibroblasts
Y Kokai, J N Myers, T Wada, et al.
Cytogenetics and Cell Genetics
|
January 1, 1997
Definition of the critical interval for Smith-Magenis syndrome
S 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 mutations
N 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 syndrome
R 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 kinetics
S 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 assembly
D 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 ancestry
R De Gasperi, M A Gama Sosa, E E Grebner, et al.
Page
of 10
Search research articles
Search
Showing results (81-90 of 97) with videos related to
Sort By:
Page
of 10
Journal of Pediatric Orthopedics
|
November 30, 2000
The incidence of protrusio acetabuli in Marfan's syndrome and its relationship to bone mineral density
T 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 potential
H 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 development
S 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 fibroblasts
Y Kokai, J N Myers, T Wada, et al.
Cytogenetics and Cell Genetics
|
January 1, 1997
Definition of the critical interval for Smith-Magenis syndrome
S 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 mutations
N 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 syndrome
R 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 kinetics
S 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 assembly
D 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 ancestry
R De Gasperi, M A Gama Sosa, E E Grebner, et al.
Page
of 10