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American Journal of Human Genetics
|
December 1, 1994
Expression, in cartilage, of a 7-amino-acid deletion in type II collagen from two unrelated individuals with Kniest dysplasia
R Bogaert, D Wilkin, W R Wilcox, et al.
The Journal of Biological Chemistry
|
December 6, 2006
Bisindolylmaleimide I suppresses fibroblast growth factor-mediated activation of Erk MAP kinase in chondrocytes by preventing Shp2 association with the Frs2 and Gab1 adaptor proteins
Pavel Krejci, Bernard Masri, Lisa Salazar, et al.
Journal of Vascular Surgery
|
September 1, 1987
The use of angiodynography to quantify blood flow in the canine aorta
B A Keagy, G J Palmer, J D Crouch, et al.
Experimental Gerontology
|
June 1, 2021
The influence of a 16-week exercise program, APOE status, and age on executive function task performance: A randomized trial
R Martin-Willett, B Morris, R Wilcox, et al.
Prehospital and Disaster Medicine
|
October 30, 2020
ECMO Transport without Physicians or Additional Clinicians
Anna Condella, Jeremy B Richards, Michael A Frakes, et al.
American Journal of Medical Genetics
|
May 26, 1998
Pacman dysplasia: report of two affected sibs
W R Wilcox, B C Lucas, B Loebel, et al.
Matrix Biology : Journal of the International Society for Matrix Biology
|
November 20, 1998
Proteoglycan sulfation in cartilage and cell cultures from patients with sulfate transporter chondrodysplasias: relationship to clinical severity and indications on the role of intracellular sulfate production
A Rossi, I Kaitila, W R Wilcox, et al.
Archives of Physical Medicine and Rehabilitation
|
December 12, 2003
Health behaviors, body composition, and coronary heart disease risk in women with multiple sclerosis
Jennifer N Slawta, Anthony R Wilcox, Jeffrey A McCubbin, et al.
American Journal of Medical Genetics
|
June 9, 1999
Platyspondylic lethal skeletal dysplasia, San Diego type, is caused by FGFR3 mutations
S G Brodie, H Kitoh, R S Lachman, et al.
Advances in Oto-Rhino-Laryngology
|
June 27, 2000
DFNB3 families and Shaker-2 mice: mutations in an unconventional myosin, myo 15
T B Friedman, J T Hinnant, R A Fridell, et al.
Page
of 80
Search research articles
Search
Showing results (491-500 of 791) with videos related to
Sort By:
Page
of 80
American Journal of Human Genetics
|
December 1, 1994
Expression, in cartilage, of a 7-amino-acid deletion in type II collagen from two unrelated individuals with Kniest dysplasia
R Bogaert, D Wilkin, W R Wilcox, et al.
The Journal of Biological Chemistry
|
December 6, 2006
Bisindolylmaleimide I suppresses fibroblast growth factor-mediated activation of Erk MAP kinase in chondrocytes by preventing Shp2 association with the Frs2 and Gab1 adaptor proteins
Pavel Krejci, Bernard Masri, Lisa Salazar, et al.
Journal of Vascular Surgery
|
September 1, 1987
The use of angiodynography to quantify blood flow in the canine aorta
B A Keagy, G J Palmer, J D Crouch, et al.
Experimental Gerontology
|
June 1, 2021
The influence of a 16-week exercise program, APOE status, and age on executive function task performance: A randomized trial
R Martin-Willett, B Morris, R Wilcox, et al.
Prehospital and Disaster Medicine
|
October 30, 2020
ECMO Transport without Physicians or Additional Clinicians
Anna Condella, Jeremy B Richards, Michael A Frakes, et al.
American Journal of Medical Genetics
|
May 26, 1998
Pacman dysplasia: report of two affected sibs
W R Wilcox, B C Lucas, B Loebel, et al.
Matrix Biology : Journal of the International Society for Matrix Biology
|
November 20, 1998
Proteoglycan sulfation in cartilage and cell cultures from patients with sulfate transporter chondrodysplasias: relationship to clinical severity and indications on the role of intracellular sulfate production
A Rossi, I Kaitila, W R Wilcox, et al.
Archives of Physical Medicine and Rehabilitation
|
December 12, 2003
Health behaviors, body composition, and coronary heart disease risk in women with multiple sclerosis
Jennifer N Slawta, Anthony R Wilcox, Jeffrey A McCubbin, et al.
American Journal of Medical Genetics
|
June 9, 1999
Platyspondylic lethal skeletal dysplasia, San Diego type, is caused by FGFR3 mutations
S G Brodie, H Kitoh, R S Lachman, et al.
Advances in Oto-Rhino-Laryngology
|
June 27, 2000
DFNB3 families and Shaker-2 mice: mutations in an unconventional myosin, myo 15
T B Friedman, J T Hinnant, R A Fridell, et al.
Page
of 80