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M A Weis

Showing results (11-20 of 19) with videos related to

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Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|November 1, 1992
A specific immunoassay for monitoring human bone resorption: quantitation of type I collagen cross-linked N-telopeptides in urineD A Hanson, M A Weis, A M Bollen, et al.
Injury Prevention : Journal of the International Society for Child and Adolescent Injury Prevention|December 16, 2006
Using NVDRS data for suicide prevention: promising practices in seven statesV Powell, C W Barber, H Hedegaard, et al.
The Journal of Clinical Investigation|October 1, 1989
Osteogenesis imperfecta. The position of substitution for glycine by cysteine in the triple helical domain of the pro alpha 1(I) chains of type I collagen determines the clinical phenotypeB J Starman, D Eyre, H Charbonneau, et al.
The Journal of Biological Chemistry|November 5, 1992
An amino acid substitution (Gly853-->Glu) in the collagen alpha 1(II) chain produces hypochondrogenesisR Bogaert, G E Tiller, M A Weis, et al.
Archives of Biochemistry and Biophysics|July 24, 1998
Incorporation of structurally defective type II collagen into cartilage matrix in kniest chondrodysplasiaR J Fernandes, D J Wilkin, M A Weis, et al.
American Journal of Human Genetics|February 1, 1995
An RNA-splicing mutation (G+5IVS20) in the type II collagen gene (COL2A1) in a family with spondyloepiphyseal dysplasia congenitaG E Tiller, M A Weis, P A Polumbo, et al.
Nature Genetics|September 1, 1995
Dominant mutations in the type II collagen gene, COL2A1, produce spondyloepimetaphyseal dysplasia, Strudwick typeG E Tiller, P A Polumbo, M A Weis, et al.
The Journal of Biological Chemistry|March 21, 1998
Structurally abnormal type II collagen in a severe form of Kniest dysplasia caused by an exon 24 skipping mutationM A Weis, D J Wilkin, H J Kim, et al.
Clinical Genetics|September 30, 2011
Deficiency of CRTAP in non-lethal recessive osteogenesis imperfecta reduces collagen deposition into matrixM Valli, A M Barnes, A Gallanti, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|November 1, 1992
A specific immunoassay for monitoring human bone resorption: quantitation of type I collagen cross-linked N-telopeptides in urineD A Hanson, M A Weis, A M Bollen, et al.
Injury Prevention : Journal of the International Society for Child and Adolescent Injury Prevention|December 16, 2006
Using NVDRS data for suicide prevention: promising practices in seven statesV Powell, C W Barber, H Hedegaard, et al.
The Journal of Clinical Investigation|October 1, 1989
Osteogenesis imperfecta. The position of substitution for glycine by cysteine in the triple helical domain of the pro alpha 1(I) chains of type I collagen determines the clinical phenotypeB J Starman, D Eyre, H Charbonneau, et al.
The Journal of Biological Chemistry|November 5, 1992
An amino acid substitution (Gly853-->Glu) in the collagen alpha 1(II) chain produces hypochondrogenesisR Bogaert, G E Tiller, M A Weis, et al.
Archives of Biochemistry and Biophysics|July 24, 1998
Incorporation of structurally defective type II collagen into cartilage matrix in kniest chondrodysplasiaR J Fernandes, D J Wilkin, M A Weis, et al.
American Journal of Human Genetics|February 1, 1995
An RNA-splicing mutation (G+5IVS20) in the type II collagen gene (COL2A1) in a family with spondyloepiphyseal dysplasia congenitaG E Tiller, M A Weis, P A Polumbo, et al.
Nature Genetics|September 1, 1995
Dominant mutations in the type II collagen gene, COL2A1, produce spondyloepimetaphyseal dysplasia, Strudwick typeG E Tiller, P A Polumbo, M A Weis, et al.
The Journal of Biological Chemistry|March 21, 1998
Structurally abnormal type II collagen in a severe form of Kniest dysplasia caused by an exon 24 skipping mutationM A Weis, D J Wilkin, H J Kim, et al.
Clinical Genetics|September 30, 2011
Deficiency of CRTAP in non-lethal recessive osteogenesis imperfecta reduces collagen deposition into matrixM Valli, A M Barnes, A Gallanti, et al.
Pageof 2