Zobrazeno 1 - 10
of 66
pro vyhledávání: '"Stephen P. Coburn"'
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
Publikováno v:
Curr Dev Nutr
OBJECTIVES: To develop a compartmental model which describes vitamin B-6 metabolism in the blood and tissues of the mouse under a variety of circumstances and to develop a computer application which can utilize the data to display the movement of tra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::114d8be797afac7f2381f54327883d08
https://europepmc.org/articles/PMC8180980/
https://europepmc.org/articles/PMC8180980/
Autor:
Stephen P. Coburn
Publikováno v:
Vitamin B-6 Metabolism in Pregnancy, Lactation, and Infancy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d79fa1446455cbc0a6ea3bb431def1b2
https://doi.org/10.1201/9781003210368-4
https://doi.org/10.1201/9781003210368-4
Autor:
Michael P, Whyte, Jennifer D, May, William H, McAlister, Katherine, Burgener, Samuel R, Cortez, Raymond, Kreienkamp, Olivia, Castro, Rachel, Verzola, Ana Solis, Zavala, Christopher C, McPherson, Gary S, Gottesman, Karen L, Ericson, Stephen P, Coburn, Ana Maria, Arbelaez
Publikováno v:
Bone. 150
Pyridoxal 5'-phosphate (PLP), the principal circulating form of vitamin B
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6940df1d945849f94c96dddbb9e2d5d5
https://pubmed.ncbi.nlm.nih.gov/34000433
https://pubmed.ncbi.nlm.nih.gov/34000433
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
Publikováno v:
Bone. 110:96-106
Hypophosphatasia (HPP) is the inborn-error-of-metabolism due to loss-of-function mutation(s) of the ALPL (TNSALP) gene that encodes the tissue non-specific isoenzyme of alkaline phosphatase (TNSALP). TNSALP represents a family of cell-surface phospho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a9f5f896e3b96d56cd4d289f42758b4
https://doi.org/10.1016/j.bone.2018.01.022
https://doi.org/10.1016/j.bone.2018.01.022
Autor:
Michael P. Whyte, Samuel R. Cortez, Katherine Burgener, Raymond Kreienkamp, William H. McAlister, Stephen P. Coburn, Ana Solis Zavala, Olivia Castro, Gary S. Gottesman, Karen L. Ericson, Rachel Verzola, Jennifer D. May, Ana Maria Arbelaez, Christopher McPherson
Publikováno v:
Bone. 150:116007
Pyridoxal 5′-phosphate (PLP), the principal circulating form of vitamin B6 (B6), is elevated in the plasma of individuals with hypophosphatasia (HPP). HPP is the inborn-error-of-metabolism caused by loss-of-function mutation(s) of ALPL, the gene th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6fe56daed5c1f2f7d798ac6951c38494
https://doi.org/10.1016/j.bone.2021.116007
https://doi.org/10.1016/j.bone.2021.116007
Autor:
Stephen P. Coburn
This review organizes the existing literature on deoxypyridoxine in order to provide additional insights for developing further work. By providing a thorough analysis of previous work with deoxypyridoxine, it can be used more effectively as a tool fo
Autor:
Carole C. Tranchant, Juliana Dosy, Marcel Caissie, Stephen P. Coburn, Priscilla G. Masse, Jean-Luc Jougleux
Publikováno v:
Journal of Clinical Biochemistry and Nutrition
Two vitamins and proline (CB(6)Pro), three nutrients essential for bone collagen, were used in combination to a 1000 mg calcium/250 IU vitamin D (Ca/D) daily supplement to treat osteopenia as a preventive measure against osteoporosis later in life. M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4aa75e15b3db5e91e3f391cf07ba648b
https://doi.org/10.3164/jcbn.09-45
https://doi.org/10.3164/jcbn.09-45
Autor:
John C. Carey, Stephen P. Coburn, Steven Mumm, Michael P. Whyte, David A. Stevenson, Janice L. B. Byrne, Karen L. Ericson
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 93:3443-3448
Context: Hypophosphatasia (HPP) is a heritable metabolic disorder of the skeleton that includes variable expressivity conditioned by gene dosage effect and the variety of mutations in the tissue nonspecific alkaline phosphatase (TNSALP) gene. Patient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d2321fcde49619e6ad71ea63d91546b
https://doi.org/10.1210/jc.2008-0318
https://doi.org/10.1210/jc.2008-0318