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Wayne A Cabral

Showing results (11-20 of 48) with videos related to

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Journal of Proteome Research|July 12, 2017
Cyclophilin B Deficiency Causes Abnormal Dentin Collagen MatrixMasahiko Terajima, Yuki Taga, Wayne A Cabral, et al.
Biomed Research International|June 27, 2013
Mineral and matrix changes in Brtl/+ teeth provide insights into mineralization mechanismsAdele L Boskey, Kostas Verdelis, Lyudmila Spevak, et al.
The Journal of Biological Chemistry|January 23, 2003
Type I collagen triplet duplication mutation in lethal osteogenesis imperfecta shifts register of alpha chains throughout the helix and disrupts incorporation of mutant helices into fibrils and extracellular matrixWayne A Cabral, Marianna V Mertts, Elena Makareeva, et al.
Human Mutation|June 22, 2012
Absence of FKBP10 in recessive type XI osteogenesis imperfecta leads to diminished collagen cross-linking and reduced collagen deposition in extracellular matrixAileen M Barnes, Wayne A Cabral, MaryAnn Weis, et al.
The Journal of Biological Chemistry|February 25, 2005
Mutations near amino end of alpha1(I) collagen cause combined osteogenesis imperfecta/Ehlers-Danlos syndrome by interference with N-propeptide processingWayne A Cabral, Elena Makareeva, Alain Colige, et al.
The Journal of Clinical Endocrinology and Metabolism|November 12, 2014
Type V OI primary osteoblasts display increased mineralization despite decreased COL1A1 expressionAdi Reich, Alison S Bae, Aileen M Barnes, et al.
Aging Cell|August 28, 2021
Genetic reduction of mTOR extends lifespan in a mouse model of Hutchinson-Gilford Progeria syndromeWayne A Cabral, Urraca L Tavarez, Indeevar Beeram, et al.
The Journal of Biological Chemistry|May 20, 2008
Mapping of SPARC/BM-40/osteonectin-binding sites on fibrillar collagensCamilla Giudici, Nicolas Raynal, Hanna Wiedemann, et al.
Human Mutation|January 9, 2007
Y-position cysteine substitution in type I collagen (alpha1(I) R888C/p.R1066C) is associated with osteogenesis imperfecta/Ehlers-Danlos syndrome phenotypeWayne A Cabral, Elena Makareeva, Anne D Letocha, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|August 8, 2008
Cellular mechanism of decreased bone in Brtl mouse model of OI: imbalance of decreased osteoblast function and increased osteoclasts and their precursorsThomas E Uveges, Patricia Collin-Osdoby, Wayne A Cabral, et al.
Pageof 5

Showing results (11-20 of 48) with videos related to

Sort By:
Pageof 5
Journal of Proteome Research|July 12, 2017
Cyclophilin B Deficiency Causes Abnormal Dentin Collagen MatrixMasahiko Terajima, Yuki Taga, Wayne A Cabral, et al.
Biomed Research International|June 27, 2013
Mineral and matrix changes in Brtl/+ teeth provide insights into mineralization mechanismsAdele L Boskey, Kostas Verdelis, Lyudmila Spevak, et al.
The Journal of Biological Chemistry|January 23, 2003
Type I collagen triplet duplication mutation in lethal osteogenesis imperfecta shifts register of alpha chains throughout the helix and disrupts incorporation of mutant helices into fibrils and extracellular matrixWayne A Cabral, Marianna V Mertts, Elena Makareeva, et al.
Human Mutation|June 22, 2012
Absence of FKBP10 in recessive type XI osteogenesis imperfecta leads to diminished collagen cross-linking and reduced collagen deposition in extracellular matrixAileen M Barnes, Wayne A Cabral, MaryAnn Weis, et al.
The Journal of Biological Chemistry|February 25, 2005
Mutations near amino end of alpha1(I) collagen cause combined osteogenesis imperfecta/Ehlers-Danlos syndrome by interference with N-propeptide processingWayne A Cabral, Elena Makareeva, Alain Colige, et al.
The Journal of Clinical Endocrinology and Metabolism|November 12, 2014
Type V OI primary osteoblasts display increased mineralization despite decreased COL1A1 expressionAdi Reich, Alison S Bae, Aileen M Barnes, et al.
Aging Cell|August 28, 2021
Genetic reduction of mTOR extends lifespan in a mouse model of Hutchinson-Gilford Progeria syndromeWayne A Cabral, Urraca L Tavarez, Indeevar Beeram, et al.
The Journal of Biological Chemistry|May 20, 2008
Mapping of SPARC/BM-40/osteonectin-binding sites on fibrillar collagensCamilla Giudici, Nicolas Raynal, Hanna Wiedemann, et al.
Human Mutation|January 9, 2007
Y-position cysteine substitution in type I collagen (alpha1(I) R888C/p.R1066C) is associated with osteogenesis imperfecta/Ehlers-Danlos syndrome phenotypeWayne A Cabral, Elena Makareeva, Anne D Letocha, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|August 8, 2008
Cellular mechanism of decreased bone in Brtl mouse model of OI: imbalance of decreased osteoblast function and increased osteoclasts and their precursorsThomas E Uveges, Patricia Collin-Osdoby, Wayne A Cabral, et al.
Pageof 5