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Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
October 20, 2005
Polymorphisms of the CLCN7 gene are associated with BMD in women
Ulrika Pettersson, Omar M E Albagha, Max Mirolo, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
November 14, 2007
A new heterozygous mutation (R714C) of the osteopetrosis gene, pleckstrin homolog domain containing family M (with run domain) member 1 (PLEKHM1), impairs vesicular acidification and increases TRACP secretion in osteoclasts
Andrea Del Fattore, Rachele Fornari, Liesbeth Van Wesenbeeck, et al.
The Journal of Biological Chemistry
|
January 14, 2016
Anabolic and Antiresorptive Modulation of Bone Homeostasis by the Epigenetic Modulator Sulforaphane, a Naturally Occurring Isothiocyanate
Roman Thaler, Antonio Maurizi, Paul Roschger, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
April 22, 2011
Mechanisms inducing low bone density in Duchenne muscular dystrophy in mice and humans
Anna Rufo, Andrea Del Fattore, Mattia Capulli, et al.
Molecular Biology of the Cell
|
April 13, 2012
NHERF1 acts as a molecular switch to program metastatic behavior and organotropism via its PDZ domains
Rosa Angela Cardone, Maria Raffaella Greco, Mattia Capulli, et al.
Journal of Science and Medicine in Sport
|
August 10, 2019
Functional polymorphisms within the inflammatory pathway regulate expression of extracellular matrix components in a genetic risk dependent model for anterior cruciate ligament injuries
Mathijs A M Suijkerbuijk, Marco Ponzetti, Masouda Rahim, et al.
Orphanet Journal of Rare Diseases
|
January 25, 2012
Novel C16orf57 mutations in patients with Poikiloderma with Neutropenia: bioinformatic analysis of the protein and predicted effects of all reported mutations
Elisa A Colombo, J Fernando Bazan, Gloria Negri, et al.
Journal of Cellular Physiology
|
September 2, 2018
Apoptosis-associated speck-like protein containing a caspase-1 recruitment domain (ASC) contributes to osteoblast differentiation and osteogenesis
Suelen Sartoretto, Sara Gemini-Piperni, Rodrigo A da Silva, et al.
Materials Science & Engineering. C, Materials for Biological Applications
|
May 16, 2020
The role of apoptosis associated speck-like protein containing a caspase-1 recruitment domain (ASC) in response to bone substitutes
Suelen C Sartoretto, Monica D Calasans-Maia, Adriana T N N Alves, et al.
Plos Medicine
|
October 14, 2015
P2RX7 purinoceptor: a therapeutic target for ameliorating the symptoms of duchenne muscular dystrophy
Anthony Sinadinos, Christopher N J Young, Rasha Al-Khalidi, et al.
Page
of 11
Search research articles
Search
Showing results (91-100 of 110) with videos related to
Sort By:
Page
of 11
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
October 20, 2005
Polymorphisms of the CLCN7 gene are associated with BMD in women
Ulrika Pettersson, Omar M E Albagha, Max Mirolo, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
November 14, 2007
A new heterozygous mutation (R714C) of the osteopetrosis gene, pleckstrin homolog domain containing family M (with run domain) member 1 (PLEKHM1), impairs vesicular acidification and increases TRACP secretion in osteoclasts
Andrea Del Fattore, Rachele Fornari, Liesbeth Van Wesenbeeck, et al.
The Journal of Biological Chemistry
|
January 14, 2016
Anabolic and Antiresorptive Modulation of Bone Homeostasis by the Epigenetic Modulator Sulforaphane, a Naturally Occurring Isothiocyanate
Roman Thaler, Antonio Maurizi, Paul Roschger, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
April 22, 2011
Mechanisms inducing low bone density in Duchenne muscular dystrophy in mice and humans
Anna Rufo, Andrea Del Fattore, Mattia Capulli, et al.
Molecular Biology of the Cell
|
April 13, 2012
NHERF1 acts as a molecular switch to program metastatic behavior and organotropism via its PDZ domains
Rosa Angela Cardone, Maria Raffaella Greco, Mattia Capulli, et al.
Journal of Science and Medicine in Sport
|
August 10, 2019
Functional polymorphisms within the inflammatory pathway regulate expression of extracellular matrix components in a genetic risk dependent model for anterior cruciate ligament injuries
Mathijs A M Suijkerbuijk, Marco Ponzetti, Masouda Rahim, et al.
Orphanet Journal of Rare Diseases
|
January 25, 2012
Novel C16orf57 mutations in patients with Poikiloderma with Neutropenia: bioinformatic analysis of the protein and predicted effects of all reported mutations
Elisa A Colombo, J Fernando Bazan, Gloria Negri, et al.
Journal of Cellular Physiology
|
September 2, 2018
Apoptosis-associated speck-like protein containing a caspase-1 recruitment domain (ASC) contributes to osteoblast differentiation and osteogenesis
Suelen Sartoretto, Sara Gemini-Piperni, Rodrigo A da Silva, et al.
Materials Science & Engineering. C, Materials for Biological Applications
|
May 16, 2020
The role of apoptosis associated speck-like protein containing a caspase-1 recruitment domain (ASC) in response to bone substitutes
Suelen C Sartoretto, Monica D Calasans-Maia, Adriana T N N Alves, et al.
Plos Medicine
|
October 14, 2015
P2RX7 purinoceptor: a therapeutic target for ameliorating the symptoms of duchenne muscular dystrophy
Anthony Sinadinos, Christopher N J Young, Rasha Al-Khalidi, et al.
Page
of 11