Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Simran Madan"'
Autor:
Simran Madan, Wei Liu, James T. Lu, V. Reid Sutton, Bryant Toth, Priscilla Joe, John R. Waterson, Richard A. Gibbs, Ignatia B. Van den Veyver, Edward J. Lammer, Philippe M. Campeau, Brendan H. Lee
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 12, Iss C, Pp 57-61 (2017)
Mutations in the PORCN gene cause the X-linked dominant condition focal dermal hypoplasia (FDH). Features of FDH include striated pigmentation of the skin, ocular and skeletal malformations. FDH is generally associated with in utero lethality in non-
Externí odkaz:
https://doaj.org/article/ecd641b746a94feca94b102c41948f68
Autor:
Balraj Singh, Anna Shamsnia, Milan R Raythatha, Ryan D Milligan, Amanda M Cady, Simran Madan, Anthony Lucci
Publikováno v:
PLoS ONE, Vol 9, Iss 10, p e109487 (2014)
A major obstacle in developing effective therapies against solid tumors stems from an inability to adequately model the rare subpopulation of panresistant cancer cells that may often drive the disease. We describe a strategy for optimally modeling hi
Externí odkaz:
https://doaj.org/article/f29eee1a74d94afcbfc5bbfad42b92a5
Autor:
Balraj Singh, Karen Tai, Simran Madan, Milan R Raythatha, Amanda M Cady, Megan Braunlin, LaTashia R Irving, Ankur Bajaj, Anthony Lucci
Publikováno v:
PLoS ONE, Vol 7, Iss 5, p e36510 (2012)
A small subpopulation of highly adaptable breast cancer cells within a vastly heterogeneous population drives cancer metastasis. Here we describe a function-based strategy for selecting rare cancer cells that are highly adaptable and drive malignancy
Externí odkaz:
https://doaj.org/article/5c8cee88622040f6b1ec30e5b57736fc
Autor:
Patricia A. Miller, Lily Freemark, Yvonne Tran, Nicole Jacobs, Natalie Chan, Geneva Kennedy, Simran Madan
Publikováno v:
The Journal of continuing education in the health professions. 42(1)
PURPOSE Clinical competence is essential for providing safe, competent care and is regularly assessed to ensure health care practitioners maintain competence. When deficiencies in competence are identified, practitioners may undergo remediation. Howe
Chronic liver disease and impaired hepatic glycogen metabolism in argininosuccinate lyase deficiency
Autor:
Zixue Jin, Bridget M. Stroup, Charles G. Minard, Sandesh C.S. Nagamani, Racel Cela, Mahmoud A. Mohammad, Lindsay C. Burrage, Daniel H. Leung, Simran Madan, Deeksha Bali, Danielle Guffey, Juan C. Marini, Milton J. Finegold, Xiaohui Li, Brendan Lee, Benjamin L. Shneider, Jian Dai, Saima Ali, Ming-Ming Jiang, Prakash Masand, Terry Bertin, Deborah Schady
Publikováno v:
JCI Insight. 5
BACKGROUND: Liver disease in urea cycle disorders (UCDs) ranges from hepatomegaly and chronic hepatocellular injury to cirrhosis and end-stage liver disease. However, the prevalence and underlying mechanisms are unclear. METHODS: We estimated the pre
Autor:
John R. Waterson, Edward J. Lammer, Bryant A. Toth, James T. Lu, V. Reid Sutton, Philippe M. Campeau, Ignatia B. Van den Veyver, Simran Madan, Richard A. Gibbs, Wei Liu, Brendan Lee, Priscilla Joe
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 12, Iss C, Pp 57-61 (2017)
Mutations in the PORCN gene cause the X-linked dominant condition focal dermal hypoplasia (FDH). Features of FDH include striated pigmentation of the skin, ocular and skeletal malformations. FDH is generally associated with in utero lethality in non-
Autor:
Yuqing Chen, Ming-Ming Jiang, Shan Chen, George Al Shamy, Leela Cherian, Zixue Jin, Clay Goodman, Brendan Lee, Elda Munivez, Philippe M. Campeau, Claudia S. Robertson, Simran Madan, Qin Sun, Bettina Kron, Rajiv R. Ratan
Publikováno v:
Molecular genetics and metabolism. 125(1-2)
Arginine is a semi-essential amino acid which serves as a substrate for nitric oxide (NO) production by nitric oxide synthase (NOS) and a precursor for various metabolites including ornithine, creatine, polyamines, and agmatine. Arginase competes wit
Autor:
Simran, Madan, Wei, Liu, James T, Lu, V Reid, Sutton, Bryant, Toth, Priscilla, Joe, John R, Waterson, Richard A, Gibbs, Ignatia B, Van den Veyver, Edward J, Lammer, Philippe M, Campeau, Brendan H, Lee
Publikováno v:
Molecular Genetics and Metabolism Reports
Mutations in the PORCN gene cause the X-linked dominant condition focal dermal hypoplasia (FDH). Features of FDH include striated pigmentation of the skin, ocular and skeletal malformations. FDH is generally associated with in utero lethality in non-
Autor:
Ryan D. Milligan, Amanda M. Cady, Anthony Lucci, Balraj Singh, Anna Shamsnia, Simran Madan, Milan R. Raythatha
Publikováno v:
PLoS ONE, Vol 9, Iss 10, p e109487 (2014)
PLoS ONE
PLoS ONE
A major obstacle in developing effective therapies against solid tumors stems from an inability to adequately model the rare subpopulation of panresistant cancer cells that may often drive the disease. We describe a strategy for optimally modeling hi
Autor:
James T. Lu, Steven Mumm, Michael P. Whyte, Richard A. Gibbs, Yangjin Bae, Ming-Ming Jiang, Brendan Lee, Philippe M. Campeau, Simran Madan, Nicholas Shaw, Gautam Sule, Wolfgang Högler
Dysosteosclerosis (DSS) is the form of osteopetrosis distinguished by the presence of skin findings such as red-violet macular atrophy, platyspondyly and metaphyseal osteosclerosis with relative radiolucency of widened diaphyses. At the histopatholog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7a13a3b8500c0e19ffc2c49ada4f950
https://europepmc.org/articles/PMC3607481/
https://europepmc.org/articles/PMC3607481/