Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Vipula Kolli"'
Autor:
Vipula Kolli, Emily Frucci, Isabela Werneck da Cunha, James R. Iben, Sun A. Kim, Ashwini Mallappa, Tianwei Li, Fabio Rueda Faucz, Electron Kebebew, Naris Nilubol, Martha M. Quezado, Deborah P. Merke
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 5, p 2543 (2024)
Adrenal myelolipomas (AML) are composed of mature adipose and hematopoietic components. They represent approximately 3 percent of adrenal tumors and are commonly found in patients with congenital adrenal hyperplasia (CAH). CAH provides a unique envir
Externí odkaz:
https://doaj.org/article/d79e885490834d05b3e53e90f06b87b3
Autor:
Vipula Kolli, Isabela Werneck da Cunha, SunA Kim, James R. Iben, Ashwini Mallappa, Tianwei Li, Alison Gaynor, Steven L. Coon, Martha M. Quezado, Deborah P. Merke
Publikováno v:
Frontiers in Endocrinology, Vol 12 (2021)
IntroductionAdrenocortical hyperplasia and adrenal rest tumor (ART) formation are common in congenital adrenal hyperplasia (CAH). Although driven by excessive corticotropin, much is unknown regarding the morphology and transformation of these tissues
Externí odkaz:
https://doaj.org/article/67e33a0b635a4f8b89d5da329b38efec
Autor:
Vipula Kolli, Hannah Kim, Hamsini Rao, Qizong Lao, Alison Gaynor, Joshua D. Milner, Deborah P. Merke
Publikováno v:
BMC Research Notes, Vol 12, Iss 1, Pp 1-6 (2019)
Abstract Objective Approximately 10% of patients with congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency carry a mutation that disrupts CYP21A2 and the flanking TNXB gene resulting in CAH-X, a contiguous gene deletion syndrome. TNX
Externí odkaz:
https://doaj.org/article/5387be3a568f4f92b26cbdf007538642
Autor:
Amit Chougule, Vipula Kolli, Sudipta Baroi, Nabil Ebraheim, Piotr J Czernik, Y Peng Loh, Beata Lecka‐Czernik
Publikováno v:
JBMR Plus, Vol 4, Iss 9, Pp n/a-n/a (2020)
ABSTRACT Bone and energy metabolism are integrated by common regulatory mechanisms. Carboxypeptidase E (CPE), also known as obesity susceptibility protein or neurotrophic factor‐α1, is recognized for its function in processing prohormones, includi
Externí odkaz:
https://doaj.org/article/a6d51828a21b4010acc55afefe998b2d
Autor:
Vipula Kolli, Lance A Stechschulte, Abigail R Dowling, Sima Rahman, Piotr J Czernik, Beata Lecka-Czernik
Publikováno v:
PLoS ONE, Vol 9, Iss 5, p e96323 (2014)
Peroxisome proliferator activated receptor gamma (PPARγ) controls both glucose metabolism and an allocation of marrow mesenchymal stem cells (MSCs) toward osteoblast and adipocyte lineages. Its activity is determined by interaction with a ligand whi
Externí odkaz:
https://doaj.org/article/af179a5352ae4948a481dd6c3308e4fe
Autor:
Chelsi Flippo, Vipula Kolli, Melissa Andrew, Seth Berger, Tricia Bhatti, Alison M Boyce, Daniel Casella, Michael T Collins, Emmanuèle Délot, Joseph Devaney, Stephen M Hewitt, Thomas Kolon, Ashwini Mallappa, Perrin C White, Deborah P Merke, Andrew Dauber
Publikováno v:
J Endocr Soc
Context Autosomal dominant and rarely de novo gain-of-function variants in the LHCGR gene are associated with precocious male puberty, while somatic LHCGR variants have been found in isolated Leydig cell adenomas and Leydig cell hyperplasia. Bilatera
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b22264b1da6a571e4780ba5b7a88822c
https://europepmc.org/articles/PMC9469925/
https://europepmc.org/articles/PMC9469925/
Autor:
Beata Lecka-Czernik, Sudipta Baroi, Y. Peng Loh, Amit Chougule, Piotr J. Czernik, Nabil A. Ebraheim, Vipula Kolli
Publikováno v:
JBMR Plus
JBMR Plus, Vol 4, Iss 9, Pp n/a-n/a (2020)
JBMR Plus, Vol 4, Iss 9, Pp n/a-n/a (2020)
Bone and energy metabolism are integrated by common regulatory mechanisms. Carboxypeptidase E (CPE), also known as obesity susceptibility protein or neurotrophic factor‐α1, is recognized for its function in processing prohormones, including proins
Autor:
Deborah P. Merke, Vipula Kolli, Christina Tatsi, Hannah Kim, Ahmed Torky, Ashwini Mallappa, Qizong Lao
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 104:269-276
Context Cholesterol side-chain cleavage enzyme (P450scc), encoded by CYP11A1, catalyzes the first step of steroidogenesis. Complete P450scc deficiency leads to primary adrenal insufficiency (PAI) and 46,XY disordered sexual development. Partial impai
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 104:1415-1416