Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Vinieth N, Bijanki"'
Publikováno v:
American Journal of Medical Quality. 38:107-109
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b6976b7bf650303a45c73b1bcceba13a
https://doi.org/10.1097/jmq.0000000000000103
https://doi.org/10.1097/jmq.0000000000000103
Autor:
Andrew Hornback, Wenqi Shi, Felipe O. Giuste, Yuanda Zhu, Ashley M. Carpenter, Coleman Hilton, Vinieth N. Bijanki, Hiram Stahl, Gary S. Gottesman, Chad Purnell, Henry J. Iwinski, J. Michael Wattenbarger, May D. Wang
Publikováno v:
Proceedings of the 13th ACM International Conference on Bioinformatics, Computational Biology and Health Informatics.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ce54c3ce5c4dc3e82ac4ae7f7fdfda24
https://doi.org/10.1145/3535508.3545565
https://doi.org/10.1145/3535508.3545565
Autor:
Michael P, Whyte, Fan, Zhang, Deborah, Wenkert, Karen E, Mack, Vinieth N, Bijanki, Karen L, Ericson, Stephen P, Coburn
Publikováno v:
Bone. 154
Hypophosphatasia (HPP) is the heritable dento-osseous disease caused by loss-of-function mutation(s) of the gene ALPL that encodes the tissue-nonspecific isoenzyme of alkaline phosphatase (TNSALP). TNSALP is a cell-surface homodimeric phosphomonoeste
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3a2aa5f7d9bed80be00bf4de590a795d
https://pubmed.ncbi.nlm.nih.gov/34547524
https://pubmed.ncbi.nlm.nih.gov/34547524
Autor:
Gary S. Gottesman, Margaret Huskey, Shenghui Duan, James Aronson, William H. McAlister, Karen L. Clements, Steven Mumm, Michael P. Whyte, Vinieth N. Bijanki, Horacio Plotkin, Marina Stolina, Robert S. Weinstein, Deborah Wenkert, Katherine L Madson
Publikováno v:
Bone. 145
In 2003, we briefly reported the remarkable osteopathy of a 12-year-old boy who at age two months began fracturing his limbs with subsequent hyperplastic callus formation and expansion and fusion of appendicular bones. By age ten years he had coalesc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ae5a553235502b13bc70d01706e1921
https://pubmed.ncbi.nlm.nih.gov/33360005
https://pubmed.ncbi.nlm.nih.gov/33360005
Autor:
Christopher M. McAndrew, Zhou Yu, Steven Mumm, Kathryn Diemer, Michael J. Gardner, Gabe Haller, Fei Wan, Melissa Sum, Yangjin Bae, Lauren E. Surface, Niki Song, Shenghui Duan, William M Ricci, Thijn R. Brummelkamp, Timothy R. Peterson, Noopur Raje, Margaret Huskey, Daniel A. Haber, Kristen M. Shannon, Sandeep Kumar, Christina L. Costantino, Jinmei Li, Jan E. Carette, Brendan Lee, Mahshid Mohseni, Jiwoong Park, Abbhirami Rajagopal, Damon T. Burrow, Malini Varadarajan, Kıvanç Birsoy, Jonathan C. Baker, Thomas B. Dodson, Charles Gu, Vinieth N. Bijanki, Cheng Lyu, Christina A. Gurnett, David M. Sabatini, Roberto Civitelli
Publikováno v:
PMC
Nitrogen-containing bisphosphonates (N-BPs), such as alendronate, are the most widely prescribed medications for diseases involving bone, with nearly 200 million prescriptions written annually. Recently, widespread use of N-BPs has been challenged du
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2223613b886c4d52ad1ac9e7f0821f2
https://doi.org/10.1126/scitranslmed.aav9166
https://doi.org/10.1126/scitranslmed.aav9166
Autor:
Nori Kurihara, Homer Sedighi, Steven Mumm, Michael P. Whyte, William H. McAlister, Deborah J. Veis, G. David Roodman, Vinieth N. Bijanki, Philippe M. Campeau, Angela Nenninger, Gary S. Gottesman, Shenghui Duan
Publikováno v:
Bone
Juvenile Paget's disease (JPD) became in 1974 the commonly used name for ultra-rare heritable occurrences of rapid bone remodeling throughout of the skeleton that present in infancy or early childhood as fractures and deformity hallmarked biochemical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5a8f7629a04e8374c56b009d6052fe8
https://europepmc.org/articles/PMC8054448/
https://europepmc.org/articles/PMC8054448/
Autor:
Per Magnusson, Nina S. Ma, Gary S. Gottesman, William H. McAlister, Karen L. Ericson, Angela Nenninger, Steven Mumm, Michael P. Whyte, Vinieth N. Bijanki
Publikováno v:
Bone. 138
Alkaline phosphatase (ALP) in humans comprises a family of four cell-surface phosphomonoester phosphohydrolase isozymes. Three genes separately encode the "tissue-specific" ALPs whereas the fourth gene encodes ubiquitous homodimeric "tissue-nonspecif
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55cc2f758efa061dc172de5729bd06af
https://pubmed.ncbi.nlm.nih.gov/32474245
https://pubmed.ncbi.nlm.nih.gov/32474245
Autor:
Vinieth N. Bijanki, Lien Trinh, Steven Mumm, Michael P. Whyte, William H. McAlister, Gary S. Gottesman, Emilina Lim, Angela Nenninger, David Buchbinder, Matthew G Boden, Deborah J. Veis
Publikováno v:
Journal of Bone and Mineral Research. 33:2071-2080
Pediatric granulomatous arthritis (PGA) refers to two formerly separate entities: autosomal dominant Blau syndrome (BS) and its sporadic phenocopy early-onset sarcoidosis (EOS). In 2001 BS and in 2005 EOS became explained by heterozygous mutations wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ed2bb45082a0741a45db3ea1ac9be4e
https://doi.org/10.1002/jbmr.3532
https://doi.org/10.1002/jbmr.3532
Autor:
Stephen P. Coburn, Fan Zhang, Karen L. Ericson, Deborah Wenkert, Karen E. Mack, Michael P. Whyte, Vinieth N. Bijanki
Publikováno v:
Bone. 154:116204
Hypophosphatasia (HPP) is the heritable dento-osseous disease caused by loss-of-function mutation(s) of the gene ALPL that encodes the tissue-nonspecific isoenzyme of alkaline phosphatase (TNSALP). TNSALP is a cell-surface homodimeric phosphomonoeste
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7bee3988030fa3cc80a1df5ff6c5c7c9
https://doi.org/10.1016/j.bone.2021.116204
https://doi.org/10.1016/j.bone.2021.116204
Autor:
Steven Mumm, Michael P. Whyte, Gary S. Gottesman, Elaine R. Mardis, Kilannin Krysiak, Lee Trani, Susan J. Bayliss, Robert Lesurf, Angela Nenninger, Vinieth N. Bijanki, Brian A. Van Tine, Obi L. Griffith, Katie M. Campbell, Malachi Griffith, Ilana S. Rosman, William H. McAlister, Zachary L. Skidmore
Publikováno v:
Bone. 101:145-155
Melorheostosis (MEL) is the rare sporadic dysostosis characterized by monostotic or polyostotic osteosclerosis and hyperostosis often distributed in a sclerotomal pattern. The prevailing hypothesis for MEL invokes postzygotic mosaicism. Sometimes scl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1c142b3f91307db7a29548aa52ff94c
https://doi.org/10.1016/j.bone.2017.04.010
https://doi.org/10.1016/j.bone.2017.04.010