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The EMBO Journal
|
October 7, 2015
Alzheimer's disease-causing proline substitutions lead to presenilin 1 aggregation and malfunction
Tziona Ben-Gedalya, Lorna Moll, Michal Bejerano-Sagie, et al.
Aging and Disease
|
November 21, 2024
Normal Bone Matrix Mineralization but Altered Growth Plate Morphology in the Lmna<sup>G609G/G609G</sup> Mouse Model of Progeria
Stéphane Blouin, Markus A Hartmann, Nadja Fratzl-Zelman, et al.
The Journal of Biological Chemistry
|
March 4, 2016
Cyclophilin-B Modulates Collagen Cross-linking by Differentially Affecting Lysine Hydroxylation in the Helical and Telopeptidyl Domains of Tendon Type I Collagen
Masahiko Terajima, Yuki Taga, Yulong Chen, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
February 13, 2014
A novel IFITM5 mutation in severe atypical osteogenesis imperfecta type VI impairs osteoblast production of pigment epithelium-derived factor
Charles R Farber, Adi Reich, Aileen M Barnes, et al.
Aging Cell
|
October 18, 2024
Angiopoietin-2 reverses endothelial cell dysfunction in progeria vasculature
Sahar Vakili, Elizabeth K Izydore, Leonhard Losert, et al.
The Journal of Biological Chemistry
|
December 13, 2007
Structural heterogeneity of type I collagen triple helix and its role in osteogenesis imperfecta
Elena Makareeva, Edward L Mertz, Natalia V Kuznetsova, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 15, 2020
Evaluation of musculoskeletal phenotype of the G608G progeria mouse model with lonafarnib, pravastatin, and zoledronic acid as treatment groups
Maria B Cubria, Sebastian Suarez, Aidin Masoudi, et al.
The New England Journal of Medicine
|
January 22, 2010
Lack of cyclophilin B in osteogenesis imperfecta with normal collagen folding
Aileen M Barnes, Erin M Carter, Wayne A Cabral, et al.
Plos Genetics
|
June 8, 2019
Cyclophilin B control of lysine post-translational modifications of skin type I collagen
Masahiko Terajima, Yuki Taga, Wayne A Cabral, et al.
Frontiers in Physiology
|
November 21, 2024
Characterization of the craniofacial abnormalities of the homozygous G608G progeria mouse model
Indeevar Beeram, Maria Belen Cubria, Pramod Kamalapathy, et al.
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Search research articles
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Showing results (21-30 of 48) with videos related to
Sort By:
Page
of 5
The EMBO Journal
|
October 7, 2015
Alzheimer's disease-causing proline substitutions lead to presenilin 1 aggregation and malfunction
Tziona Ben-Gedalya, Lorna Moll, Michal Bejerano-Sagie, et al.
Aging and Disease
|
November 21, 2024
Normal Bone Matrix Mineralization but Altered Growth Plate Morphology in the Lmna<sup>G609G/G609G</sup> Mouse Model of Progeria
Stéphane Blouin, Markus A Hartmann, Nadja Fratzl-Zelman, et al.
The Journal of Biological Chemistry
|
March 4, 2016
Cyclophilin-B Modulates Collagen Cross-linking by Differentially Affecting Lysine Hydroxylation in the Helical and Telopeptidyl Domains of Tendon Type I Collagen
Masahiko Terajima, Yuki Taga, Yulong Chen, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
February 13, 2014
A novel IFITM5 mutation in severe atypical osteogenesis imperfecta type VI impairs osteoblast production of pigment epithelium-derived factor
Charles R Farber, Adi Reich, Aileen M Barnes, et al.
Aging Cell
|
October 18, 2024
Angiopoietin-2 reverses endothelial cell dysfunction in progeria vasculature
Sahar Vakili, Elizabeth K Izydore, Leonhard Losert, et al.
The Journal of Biological Chemistry
|
December 13, 2007
Structural heterogeneity of type I collagen triple helix and its role in osteogenesis imperfecta
Elena Makareeva, Edward L Mertz, Natalia V Kuznetsova, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 15, 2020
Evaluation of musculoskeletal phenotype of the G608G progeria mouse model with lonafarnib, pravastatin, and zoledronic acid as treatment groups
Maria B Cubria, Sebastian Suarez, Aidin Masoudi, et al.
The New England Journal of Medicine
|
January 22, 2010
Lack of cyclophilin B in osteogenesis imperfecta with normal collagen folding
Aileen M Barnes, Erin M Carter, Wayne A Cabral, et al.
Plos Genetics
|
June 8, 2019
Cyclophilin B control of lysine post-translational modifications of skin type I collagen
Masahiko Terajima, Yuki Taga, Wayne A Cabral, et al.
Frontiers in Physiology
|
November 21, 2024
Characterization of the craniofacial abnormalities of the homozygous G608G progeria mouse model
Indeevar Beeram, Maria Belen Cubria, Pramod Kamalapathy, et al.
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of 5