Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Catherine L Omosule"'
Autor:
Catherine L. Omosule, Dominique Joseph, Brooke Weiler, Victoria L. Gremminger, Spencer Silvey, Brittany N. Lafaver, Youngjae Jeong, Sandra Kleiner, Charlotte L. Phillips
Publikováno v:
JBMR Plus, Vol 7, Iss 7, Pp n/a-n/a (2023)
ABSTRACT Mutations in the COL1A1 and COL1A2 genes, which encode type I collagen, are present in around 85%–90% of osteogenesis imperfecta (OI) patients. Because type I collagen is the principal protein composition of bones, any changes in its gene
Externí odkaz:
https://doaj.org/article/61f08036987e43cb991d7bce5a951fec
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Current research findings in humans and other mammalian and non-mammalian species support the potent regulatory role of myostatin in the morphology and function of muscle as well as cellular differentiation and metabolism, with real-life implications
Externí odkaz:
https://doaj.org/article/5a84882d06de407b8c37d2c833464d8f
Autor:
Catherine L Omosule, Karl G Hock, Claire Dalton, Anthony Scalpati, Ann M Gronowski, Aigars Brants, Christopher W Farnsworth
Publikováno v:
The Journal of Applied Laboratory Medicine.
Background The Freelite assay (The Binding Site) is utilized to quantify serum immunoglobulin free light chains (sFLC), which is crucial for diagnosing and monitoring plasma cell dyscrasias (PCDs). Using the Freelite test, we compared methods and eva
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e229ddac29e7947285495494daa32ef2
https://doi.org/10.1093/jalm/jfad020
https://doi.org/10.1093/jalm/jfad020
Autor:
Catherine L. Omosule, Dominique Joseph, Brooke Weiler, Victoria L. Gremminger, Spencer Silvey, Youngjae Jeong, Ashique Rafique, Pamela Krueger, Sandra Kleiner, Charlotte L. Phillips
Publikováno v:
J Bone Miner Res
Osteogenesis imperfecta (OI) is a collagen-related bone disorder characterized by fragile osteopenic bone and muscle weakness. We have previously shown that the soluble activin receptor type IIB decoy (sActRIIB) molecule increases muscle mass and imp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91b8fed6384a975516bde9a3fb8ca49e
https://doi.org/10.1002/jbmr.4529
https://doi.org/10.1002/jbmr.4529
Publikováno v:
The journal of applied laboratory medicine.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09deb20954de7e7536c54c88ca91a807
https://pubmed.ncbi.nlm.nih.gov/36533488
https://pubmed.ncbi.nlm.nih.gov/36533488
Autor:
null Catherine L. Omosule, null Dominique Joseph, null Brooke Weiler, null Victoria L. Gremminger, null Spencer Silvey, null Youngjae Jeong, null Ashique Rafique, null Pamela Krueger, null Sandra Kleiner, null Charlotte L. Phillips
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::75b885ad191f257372858c5d904bfb05
https://doi.org/10.1002/jbmr.4529/v2/response1
https://doi.org/10.1002/jbmr.4529/v2/response1
Publikováno v:
Clinical biochemistry. 104
Measurement of ionized calcium (iCa) reflects bioavailable calcium and has significant utility in children. However, robust pediatric iCa reference intervals (RI) have not been well-established. In this study, we retrospectively calculated RI for iCa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b03c36066dac2bcdb6166bef9d67f300
https://pubmed.ncbi.nlm.nih.gov/35288108
https://pubmed.ncbi.nlm.nih.gov/35288108
Autor:
Victoria L. Gremminger, Catherine L. Omosule, Tara K. Crawford, Rory Cunningham, R. Scott Rector, Charlotte L. Phillips
Publikováno v:
Molecular genetics and metabolism. 136(4)
Osteogenesis imperfecta (OI) is rare heritable connective tissue disorder that most often arises from mutations in the type I collagen genes, COL1A1 and COL1A2, displaying a range of symptoms including skeletal fragility, short stature, blue-gray scl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c2fb58f182067f4d9f19f1658c54439
https://pubmed.ncbi.nlm.nih.gov/35725939
https://pubmed.ncbi.nlm.nih.gov/35725939
Autor:
Anqing Zhang, Jason Mastaitis, Victoria L Gremminger, Ferris M. Pfeiffer, Ashley M. Aguillard, Ashique Rafique, Lawrence Miloscio, Catherine L. Omosule, Youngjae Jeong, Laura C. Schulz, Emily N. Harrelson, Charlotte L. Phillips, Sandra Kleiner
Publikováno v:
J Bone Miner Res
Osteogenesis imperfecta (OI) is a genetic connective tissue disorder characterized by compromised skeletal integrity, altered microarchitecture, and bone fragility. Current OI treatment strategies focus on bone antiresorptives and surgical interventi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0ceb02b8b1dea5c5e07fd0fa55cbd6b
https://europepmc.org/articles/PMC8111798/
https://europepmc.org/articles/PMC8111798/
Autor:
Ferris M. Pfeiffer, Sandra Kleiner, Lawrence Miloscio, Catherine L. Omosule, Jason Mastaitis, Ashley M. Aguillard, Youngjae Jeong, Emily N. Harrelson, Anqing Zhang, Ashique Rafique, Victoria L Gremminger, Laura C. Schulz, Charlotte L. Phillips
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::50c54211d0bb507ad16ce2969a05bd2c
https://doi.org/10.1002/jbmr.4223/v2/response1
https://doi.org/10.1002/jbmr.4223/v2/response1