Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Christine T. Ferrara"'
Autor:
Christine T. Ferrara, Ping Wang, Elias Chaibub Neto, Robert D. Stevens, James R. Bain, Brett R. Wenner, Olga R. Ilkayeva, Mark P. Keller, Daniel A. Blasiole, Christina Kendziorski, Brian S. Yandell, Christopher B. Newgard, Alan D. Attie
Publikováno v:
PLoS Genetics, Vol 4, Iss 7 (2008)
Externí odkaz:
https://doaj.org/article/486ac618ed3d4cccbb84260f52989e48
Autor:
Ayca Erkin-Cakmak, Gina Capodanno, Stephen E. Gitelman, Christine T. Ferrara, Hannah Chesser, Joseph T. Shieh
Publikováno v:
Journal of the Endocrine Society
Background: Congenital hyperinsulinism (HI) is the leading cause of severe, persistent hypoglycemia in infants. Transient HI seen at risk neonates due to prenatal stress and some of the congenital HI cases due to mutations in K-ATPase channel are res
Disruptions of growth and puberty are typically the first signs of an endocrine disorder. Using vignettes and a question-and-answer format, this chapter discusses common and uncommon cases of hormone dysfunction presenting from infancy through adoles
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d307b17c4307c5b838dee6122e3c802e
https://doi.org/10.1093/med/9780190848712.003.0012
https://doi.org/10.1093/med/9780190848712.003.0012
Autor:
Christine T Ferrara, Ping Wang, Elias Chaibub Neto, Robert D Stevens, James R Bain, Brett R Wenner, Olga R Ilkayeva, Mark P Keller, Daniel A Blasiole, Christina Kendziorski, Brian S Yandell, Christopher B Newgard, Alan D Attie
Publikováno v:
PLoS Genetics, Vol 4, Iss 3, p e1000034 (2008)
Although numerous quantitative trait loci (QTL) influencing disease-related phenotypes have been detected through gene mapping and positional cloning, identification of the individual gene(s) and molecular pathways leading to those phenotypes is ofte
Externí odkaz:
https://doaj.org/article/48e820b028a54bf79bb5efbff00034d9
Autor:
Maria J. Redondo, Antoinette Moran, Stephen E. Gitelman, Ingrid Libman, John M. Wentworth, Dorothy J. Becker, Carmella Evans-Molina, Susan Geyer, Christine T. Ferrara
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 102:4596-4603
Background Given the global rise in both type 1 diabetes incidence and obesity, the role of body mass index (BMI) on type 1 diabetes pathophysiology has gained great interest. Sustained excess BMI in pediatric participants of the TrialNet Pathway to
Publikováno v:
The Journal of Pediatrics. 168:212-219
To evaluate thresholds of various biomarkers for defining excess insulin activity to recognize congenital hyperinsulinism.This was a retrospective chart review of diagnostic fasting tests in children with ketotic hypoglycemia (n = 30) and genetically
Autor:
Roger K. Long, Christine T. Ferrara, Stephen E. Gitelman, Michael S. German, Shi-Bing Yang, Yen-Yu Yang
Publikováno v:
Channels, vol 11, iss 6
Channels
Channels
The ATP-sensitive potassium channel (KATP) functions as a metabo-electric transducer in regulating insulin secretion from pancreatic β-cells. The pancreatic KATP channel is composed of a pore-forming inwardly-rectifying potassium channel, Kir6.2, an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::412e8f542c0e11019b3cce92fd63850f
https://escholarship.org/uc/item/7rz565d8
https://escholarship.org/uc/item/7rz565d8
Publikováno v:
Pediatrics. 140
* Abbreviations: CD — : celiac disease T1D — : type 1 diabetes TEDDY — : The Environmental Determinants of Diabetes in the Young Celiac disease (CD) and type 1 diabetes (T1D) are T-cell mediated autoimmune diseases that have several overlapping
Autor:
Eveline O. Stock, Mary J. Malloy, Christine T. Ferrara, Josefina Naya-Vigne, John P. Kane, Clive R. Pullinger, Philip H. Frost, Patricia O’Connor
Publikováno v:
Journal of clinical lipidology. 12(1)
Background Prebeta-1 high-density lipoprotein (HDL) is a small subspecies of HDL that functions as the HDL quantum particle and is the principal acceptor of cholesterol effluxed from macrophages through the ATP-binding cassette transporter, ABCA1. Hi
Autor:
Eleonora Paradies, Arupa Ganguly, Linda Steinkrauss, Diva D. De León, Jose Bernardo Quintos, Ferdinando Palmieri, Lisa Swartz Topor, Kara E. Boodhansingh, Charles A. Stanley, Fiermonte Giuseppe, Christine T. Ferrara
Publikováno v:
The Journal of clinical endocrinology and metabolism 102 (2017): 942–949. doi:10.1210/jc.2016-3164
info:cnr-pdr/source/autori:Ferrara C.T.; Boodhansingh K.E.; Paradies E.; Giuseppe F.; Steinkrauss L.J.; Topor L.S.; Quintos J.B.; Ganguly A.; De Leon D.D.; Palmieri F.; Stanley C.A./titolo:Novel hypoglycemia phenotype in congenital hyperinsulinism due to dominant mutations of uncoupling protein 2/doi:10.1210%2Fjc.2016-3164/rivista:The Journal of clinical endocrinology and metabolism/anno:2017/pagina_da:942/pagina_a:949/intervallo_pagine:942–949/volume:102
info:cnr-pdr/source/autori:Ferrara C.T.; Boodhansingh K.E.; Paradies E.; Giuseppe F.; Steinkrauss L.J.; Topor L.S.; Quintos J.B.; Ganguly A.; De Leon D.D.; Palmieri F.; Stanley C.A./titolo:Novel hypoglycemia phenotype in congenital hyperinsulinism due to dominant mutations of uncoupling protein 2/doi:10.1210%2Fjc.2016-3164/rivista:The Journal of clinical endocrinology and metabolism/anno:2017/pagina_da:942/pagina_a:949/intervallo_pagine:942–949/volume:102
Context The rarest genetic form of congenital hyperinsulinism (HI) has been associated with dominant inactivating mutations in uncoupling protein 2 (UCP2), a mitochondrial inner membrane carrier that modulates oxidation of glucose vs amino acids. Obj
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe310ad587cc954a2f797bd8dc28b125
http://www.cnr.it/prodotto/i/369774
http://www.cnr.it/prodotto/i/369774