Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Kyle P. McNerney"'
Autor:
Andrew J. Bauer, Bethany Auble, Amy L. Clark, Tina Y. Hu, Amber Isaza, Kyle P. McNerney, Daniel L. Metzger, Lindsey Nicol, Samuel R. Pierce, Richard Sidlow
Publikováno v:
Frontiers in Pediatrics, Vol 12 (2024)
Monocarboxylate transporter 8 (MCT8) deficiency is a rare, X-linked disorder arising from mutations in the SLC16A2 gene and resulting from dysfunctional thyroid hormone transport. This disorder is characterized by profound neurodevelopmental delay an
Externí odkaz:
https://doaj.org/article/9aa8cd96d30c4def9908a9d3f71c8e2b
Autor:
Jisu Oh, Amy E. Riek, Kevin T. Bauerle, Adriana Dusso, Kyle P. McNerney, Ruteja A. Barve, Isra Darwech, Jennifer E. Sprague, Clare Moynihan, Rong M. Zhang, Greta Kutz, Ting Wang, Xiaoyun Xing, Daofeng Li, Marguerite Mrad, Nicholas M. Wigge, Esmeralda Castelblanco, Alejandro Collin, Monika Bambouskova, Richard D. Head, Mark S. Sands, Carlos Bernal-Mizrachi
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-18 (2023)
Abstract Environmental factors may alter the fetal genome to cause metabolic diseases. It is unknown whether embryonic immune cell programming impacts the risk of type 2 diabetes in later life. We demonstrate that transplantation of fetal hematopoiet
Externí odkaz:
https://doaj.org/article/006bb5f74e894a5ca7b478ca55888534
Autor:
Einas H. Alkhatib, Jody B. Grundman, Anna M. Adamusiak, Melena D. Bellin, Joel P. Brooks, Kevin S. Buckley, Erin M. Janssen, Maleewan Kitcharoensakkul, Kyle P. McNerney, Thea L. Pfeifer, Brooke I. Polk, Brynn E. Marks
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
ObjectiveImmediate type I, type III, and delayed type IV hypersensitivity reactions to insulin are rare, but potentially serious complications of exogenous insulin administration required for the treatment of type 1 diabetes (T1D).MethodsWe present f
Externí odkaz:
https://doaj.org/article/67260d91f03d434c969145a124ce0cf5
Autor:
Kyle P. McNerney, Ana Maria Arbeláez
Publikováno v:
NeoReviews. 24:e207-e216
The adrenal gland cortex produces life-sustaining steroid hormones that are critical for the development and survival of the fetus and neonate. Antenatal and postnatal administration of steroids has critical therapeutic effects in preterm infants. Ho
Autor:
Jisu Oh, Amy E. Riek, Kevin T. Bauerle, Adriana Dusso, Kyle P. McNerney, Ruteja A. Barve, Isra Darwech, Jennifer Sprague, Clare Moynihan, Rong M Zhang, Ting Wang, Xiaoyun Xing, Daofeng Li, Richard D. Head, Monika Bambouskova, Marguerite Mrad, Alejandro Collins, Mark S. Sands, Carlos Bernal-Mizrachi
Environmental factors may alter the fetal genome to cause metabolic diseases. It is unknown whether embryonic immune cell programming impacts the risk of type 2 diabetes in later life. We demonstrate that transplantation of fetal hematopoietic stem c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7c37639e53868c652b29c0eceabbc834
https://doi.org/10.1101/2022.09.08.507174
https://doi.org/10.1101/2022.09.08.507174
Autor:
Kyle P. McNerney, Ana Maria Arbeláez
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism.
Objectives The diagnosis of adrenal insufficiency relies on clear cut-offs and accurate measurement of cortisol levels. Newer monoclonal antibody assays may increase the rate of diagnosis of adrenal insufficiency if traditional cortisol cut-off level
Publikováno v:
Acta Physiol (Oxf)
Hypertension is the primary cause of cardiovascular mortality. Despite multiple existing treatments, only half of those with the disease achieve adequate control. Therefore, understanding the mechanisms causing hypertension is essential for the devel
Publikováno v:
Journal of the Endocrine Society
Background: Vitamin D deficiency is prevalent in pregnant women and their offspring. Maternal vitamin D deficiency is associated with insulin resistance in children and can induce a proinflammatory macrophage phenotype [1, 2]. Purpose: We hypothesize