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American Journal of Medical Genetics
|
September 1, 1989
Type I procollagen: the gene-protein system that harbors most of the mutations causing osteogenesis imperfecta and probably more common heritable disorders of connective tissue
D J Prockop, C D Constantinou, K E Dombrowski, et al.
Human Genetics
|
June 1, 1994
A base substitution at IVS-19 3'-end splice junction causes exon 20 skipping in pro alpha 2(I) collagen mRNA and produces mild osteogenesis imperfecta
M Mottes, A Sangalli, M Valli, et al.
The Journal of Biological Chemistry
|
November 15, 1991
The substitution of arginine for glycine 85 of the alpha 1(I) procollagen chain results in mild osteogenesis imperfecta. The mutation provides direct evidence for three discrete domains of cooperative melting of intact type I collagen
S B Deak, P M Scholz, P S Amenta, et al.
Matrix (Stuttgart, Germany)
|
April 1, 1992
Three new polymorphisms at the COL1A2 locus
D Strobel, T Tsuneyoshi, H Kuivaniemi, et al.
Nature Genetics
|
December 1, 1993
Chromosome 4 localization of a second gene for autosomal dominant polycystic kidney disease
D J Peters, L Spruit, J J Saris, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
June 1, 1994
Mutation analysis of coding sequences for type I procollagen in individuals with low bone density
L D Spotila, A Colige, L Sereda, et al.
Genomics
|
May 1, 1992
An error in dystrophin mRNA processing in golden retriever muscular dystrophy, an animal homologue of Duchenne muscular dystrophy
N J Sharp, J N Kornegay, S D Van Camp, et al.
Clinical Oncology (Royal College of Radiologists (Great Britain))
|
November 10, 2024
OSAIRIS: Lessons Learned From the Hospital-Based Implementation and Evaluation of an Open-Source Deep-Learning Model for Radiotherapy Image Segmentation
A D Constantinou, A Hoole, D C Wong, et al.
Page
of 5
Search research articles
Search
Showing results (41-50 of 48) with videos related to
Sort By:
Page
of 5
You have reached the last page of results.
This site can display upto 48 results.
American Journal of Medical Genetics
|
September 1, 1989
Type I procollagen: the gene-protein system that harbors most of the mutations causing osteogenesis imperfecta and probably more common heritable disorders of connective tissue
D J Prockop, C D Constantinou, K E Dombrowski, et al.
Human Genetics
|
June 1, 1994
A base substitution at IVS-19 3'-end splice junction causes exon 20 skipping in pro alpha 2(I) collagen mRNA and produces mild osteogenesis imperfecta
M Mottes, A Sangalli, M Valli, et al.
The Journal of Biological Chemistry
|
November 15, 1991
The substitution of arginine for glycine 85 of the alpha 1(I) procollagen chain results in mild osteogenesis imperfecta. The mutation provides direct evidence for three discrete domains of cooperative melting of intact type I collagen
S B Deak, P M Scholz, P S Amenta, et al.
Matrix (Stuttgart, Germany)
|
April 1, 1992
Three new polymorphisms at the COL1A2 locus
D Strobel, T Tsuneyoshi, H Kuivaniemi, et al.
Nature Genetics
|
December 1, 1993
Chromosome 4 localization of a second gene for autosomal dominant polycystic kidney disease
D J Peters, L Spruit, J J Saris, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
June 1, 1994
Mutation analysis of coding sequences for type I procollagen in individuals with low bone density
L D Spotila, A Colige, L Sereda, et al.
Genomics
|
May 1, 1992
An error in dystrophin mRNA processing in golden retriever muscular dystrophy, an animal homologue of Duchenne muscular dystrophy
N J Sharp, J N Kornegay, S D Van Camp, et al.
Clinical Oncology (Royal College of Radiologists (Great Britain))
|
November 10, 2024
OSAIRIS: Lessons Learned From the Hospital-Based Implementation and Evaluation of an Open-Source Deep-Learning Model for Radiotherapy Image Segmentation
A D Constantinou, A Hoole, D C Wong, et al.
Page
of 5