Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Chaitali Misra"'
Autor:
Chaitali Misra, Nita Sachan, Caryn Rothrock McNally, Sara N Koenig, Haley A Nichols, Anuradha Guggilam, Pamela A Lucchesi, William T Pu, Deepak Srivastava, Vidu Garg
Publikováno v:
PLoS Genetics, Vol 8, Iss 5, p e1002690 (2012)
Defects of atrial and ventricular septation are the most frequent form of congenital heart disease, accounting for almost 50% of all cases. We previously reported that a heterozygous G296S missense mutation of GATA4 caused atrial and ventricular sept
Externí odkaz:
https://doaj.org/article/8e619ecf80d14f26a44be5766806ce46
Publikováno v:
Circulation Research. 129
Myotonic Dystrophy type 1 (DM1), the most prevalent form of adult-onset muscular dystrophy, is caused by CTG trinucleotide repeat expansion in the 3’-UTR of the DMPK gene. Heart dysfunctions occur in nearly 80% of DM1 patients, and cardiac arrhythm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::009f4687cf3e267fc2e687d187bd1a77
https://doi.org/10.1161/res.129.suppl_1.mp249
https://doi.org/10.1161/res.129.suppl_1.mp249
Publikováno v:
Circulation Research. 127
Myotonic Dystrophy type 1 (DM1), the most prevalent form of adult onset muscular dystrophy, is caused by CTG trinucleotide repeat expansion in the 3’-UTR of DMPK gene. Over 80% of DM1 patients exhibit heart dysfunctions, which are the second leadin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::92facaafffd62b9b40b215b83adcb581
https://doi.org/10.1161/res.127.suppl_1.531
https://doi.org/10.1161/res.127.suppl_1.531
Autor:
Emad Tajkhorshid, Lawrence W. Dobrucki, Jamila Hedhli, Thomas A. Cooper, Chaitali Misra, Feikai Lin, Darren J. Parker, Nathaniel P. Murphy, Peter J. Mohler, Kin Lam, Sara N. Koenig, Sushant Bangru, Auinash Kalsotra, Ellen R. Lubbers
SUMMARYMyotonic dystrophy type 1 (DM1) is a multisystemic genetic disorder caused by a CTG trinucleotide repeat expansion in the 3′ untranslated region ofDMPKgene. Heart dysfunctions occur in nearly 80% of DM1 patients and are the second leading ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::774fdc95c19b27ace09a1a865bda6569
https://doi.org/10.1101/649715
https://doi.org/10.1101/649715
Autor:
Sushant Bangru, Auinash Kalsotra, Ellen R. Lubbers, Jamila Hedhli, Thomas A. Cooper, Sara N. Koenig, Chaitali Misra, Darren J. Parker, Wawrzyniec Dobrucki, Peter J. Mohler
Publikováno v:
Circulation Research. 123
Myotonic dystrophy type 1 (DM1) is a dominantly inherited neuromuscular disease caused by a CTG repeat expansion in 3’-UTR of DMPK gene. DM1 affects multiple tissues, but cardiac dysfunctions are the second leading cause of death which often includ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6b03181fad2e1ac7000a68ced96eefda
https://doi.org/10.1161/res.123.suppl_1.520
https://doi.org/10.1161/res.123.suppl_1.520
Publikováno v:
Human Molecular Genetics. 23:5025-5035
Mutations in GATA4 and TBX5 are associated with congenital heart defects in humans. Interaction between GATA4 and TBX5 is important for normal cardiac septation, but the underlying molecular mechanisms are not well understood. Here, we show that Gata
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e4a30cfd0f31955d53095c3155611f9
https://doi.org/10.1093/hmg/ddu215
https://doi.org/10.1093/hmg/ddu215
Autor:
AMIT MITRA, Chaitali Misra, Archana Singh, Ikhlak Ahmed, Mahua Maulik, Jyotsna Batra, Giriraj Ratan Chandak, Sandeep Grover, Rubina Tabassum, Tavpritesh Sethi
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 97:E1820-E1824
The pathogenesis of isolated hypoparathyroidism, also referred to as idiopathic hypoparathyroidism (IH), is not clear. There is a paucity of information related to the immunogenetic basis of the disease due to its rarity. A recurrent theme of several
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b3cdc66fea628d2f76cc7a9c509bb12
https://doi.org/10.1210/jc.2012-1328
https://doi.org/10.1210/jc.2012-1328
Publikováno v:
Journal of Hydrologic Engineering. 17:694-703
A dynamic subtime-stepping method is described for solving contaminant transport problems that utilize higher-order implicit time-marching procedures with higher-accuracy nonoscillating spatial-discretization methods to resolve sharp-plume fronts in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::857e574f91e679e01aab883cd33e2799
https://doi.org/10.1061/(asce)he.1943-5584.0000507
https://doi.org/10.1061/(asce)he.1943-5584.0000507
Autor:
Chaitali Misra, Subimal Ghosh
Publikováno v:
The Open Hydrology Journal. 4:115-121
Climate Change refers to any systematic change in the long-term statistics of climate elements (such as tem- perature, pressure, or winds) sustained over several decades or longer time periods. General Circulation Models (GCMs) are tools designed to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a41365cf3a1f25900d766231cbbbb8eb
https://doi.org/10.2174/1874378101004010115
https://doi.org/10.2174/1874378101004010115
Publikováno v:
Journal of Clinical Pathology. 58:26-31
Background: The predictive value of codon 72 arginine homozygosity at the p53 gene for human papilloma virus associated cervical cancer risk remains inconclusive. It has also been proposed that the inheritance of specific germline haplotypes based on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e2c66350cdc269b37b896af43bd4708
https://doi.org/10.1136/jcp.2004.019315
https://doi.org/10.1136/jcp.2004.019315