Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Priyaanka Nanduri"'
Autor:
Britney L Grayson, Mary Ellen Smith, James W Thomas, Lily Wang, Phil Dexheimer, Joy Jeffrey, Pamela R Fain, Priyaanka Nanduri, George S Eisenbarth, Thomas M Aune
Publikováno v:
PLoS ONE, Vol 5, Iss 11, p e15393 (2010)
Type 1 diabetes (T1D) tends to cluster in families, suggesting there may be a genetic component predisposing to disease. However, a recent large-scale genome-wide association study concluded that identified genetic factors, single nucleotide polymorp
Externí odkaz:
https://doaj.org/article/1b7c2731cbc94c4897e2e37fb8eea750
Publikováno v:
Journal of Biological Chemistry. 290:9455-9464
Efficient elimination of misfolded proteins by the proteasome system is critical for proteostasis. Inadequate proteasome capacity can lead to aberrant aggregation of misfolded proteins and inclusion body formation, a hallmark of neurodegenerative dis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0247e0722415b96c18c43496cfcef72
https://doi.org/10.1074/jbc.m114.627950
https://doi.org/10.1074/jbc.m114.627950
Autor:
Yanhua Rao, Minoru Yoshida, Rui Hao, Priyaanka Nanduri, Akihiro Ito, Tso-Pang Yao, R. Scott Panichelli
Publikováno v:
Molecular Cell. 51(6):819-828
Aberrant protein aggregation is a dominant pathological feature in neurodegenerative diseases. Protein aggregates cannot be processed by the proteasome; instead, they are frequently concentrated to a perinuclear inclusion body, the aggresome, and sub
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5795e222390d169ddf9baa604672f792
Autor:
Georgeanna J. Klingensmith, Liping Yu, George S. Eisenbarth, Peter A. Gottlieb, Jennifer M. Barker, Peter R. Baker, Priyaanka Nanduri
Publikováno v:
Clinical Endocrinology. 76:617-624
Context Autoantibodies to 21-hydroxylase (21OH-AA) precede onset of autoimmune Addison's disease (AD). Progression to AD can take months to years, and early detection of metabolic decompensation may prevent morbidity and mortality.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b0a8ed7ecadbec228ffeb56b54d4a9a4
https://doi.org/10.1111/j.1365-2265.2011.04276.x
https://doi.org/10.1111/j.1365-2265.2011.04276.x
Autor:
Peter A. Gottlieb, Peter R. Baker, Janet C. Siebert, Marian Rewers, Priyaanka Nanduri, Pam R. Fain, Taylor M. Triolo, Taylor K. Armstrong, Sunanda R. Babu, Erin E. Baschal, George S. Eisenbarth, Jennifer M. Barker
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 96:2154-2162
Autoimmune Addison's disease (AD) is the major cause of primary adrenal failure in developed nations. Autoantibodies to 21-hydroxylase (21OH-AA) are associated with increased risk of progression to AD. Highest genetic risk is associated with the Majo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a215f0025989bc133725b90f3d1679b
https://doi.org/10.1210/jc.2010-2964
https://doi.org/10.1210/jc.2010-2964
Autor:
Peter R, Baker, Priyaanka, Nanduri, Peter A, Gottlieb, Liping, Yu, Georgeanna J, Klingensmith, George S, Eisenbarth, Jennifer M, Barker
Publikováno v:
Clinical endocrinology. 76(5)
Autoantibodies to 21-hydroxylase (21OH-AA) precede onset of autoimmune Addison's disease (AD). Progression to AD can take months to years, and early detection of metabolic decompensation may prevent morbidity and mortality.To define optimal methods o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5dc4cec49565c85ac39a3cf1de3e9d58
https://pubmed.ncbi.nlm.nih.gov/22066755
https://pubmed.ncbi.nlm.nih.gov/22066755
Autor:
Phil Dexheimer, Joy Jeffrey, Lily Wang, James W. Thomas, Britney L. Grayson, Pamela R. Fain, Priyaanka Nanduri, George S. Eisenbarth, Mary Ellen Smith, Thomas M. Aune
Publikováno v:
PLoS ONE, Vol 5, Iss 11, p e15393 (2010)
PLoS ONE
PLoS ONE
Type 1 diabetes (T1D) tends to cluster in families, suggesting there may be a genetic component predisposing to disease. However, a recent large-scale genome-wide association study concluded that identified genetic factors, single nucleotide polymorp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27e264bbb5c1800822118bb2f0fe4c81
http://europepmc.org/articles/PMC2981564?pdf=render
http://europepmc.org/articles/PMC2981564?pdf=render
Autor:
Marian Rewers, George S. Eisenbarth, Janet C. Siebert, Taylor M. Triolo, Sunanda R. Babu, Taylor K. Armstrong, Peter R. Baker, Pam R. Fain, Jennifer M. Barker, Priyaanka Nanduri, Peter A. Gottlieb, Erin E. Baschal
Publikováno v:
The Journal of clinical endocrinology and metabolism. 95(10)
Context: Multiple autoimmune disorders (e.g. Addison’s disease, type 1 diabetes, celiac disease) are associated with HLA-DR3, but it is likely that alleles of additional genes in linkage disequilibrium with HLA-DRB1 contribute to disease. Objective
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::916487034a72c90086572243871d1296
https://pubmed.ncbi.nlm.nih.gov/20631027
https://pubmed.ncbi.nlm.nih.gov/20631027