Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Reshmi Chowdhury"'
Publikováno v:
G3: Genes, Genomes, Genetics, Vol 6, Iss 12, Pp 3995-4007 (2016)
Meiotic recombination is an essential step in gametogenesis, and is one that also generates genetic diversity. Genome-wide association studies (GWAS) and molecular studies have identified genes that influence of human meiotic recombination. RNF212 is
Externí odkaz:
https://doaj.org/article/eb0b611412e54bff9d91e8eea8dcdea9
Autor:
Tiffany Renee Oliver, Candace D Middlebrooks, Stuart W Tinker, Emily Graves Allen, Lora J H Bean, Ferdouse Begum, Eleanor Feingold, Reshmi Chowdhury, Vivian Cheung, Stephanie L Sherman
Publikováno v:
PLoS ONE, Vol 9, Iss 6, p e99560 (2014)
Trisomy 21, resulting in Down Syndrome (DS), is the most common autosomal trisomy among live-born infants and is caused mainly by nondisjunction of chromosome 21 within oocytes. Risk factors for nondisjunction depend on the parental origin and type o
Externí odkaz:
https://doaj.org/article/4dfaa2cbb5d54f1e8ee39c1a21c88da9
Publikováno v:
PLoS Genetics, Vol 5, Iss 9, p e1000648 (2009)
The number of recombination events per meiosis varies extensively among individuals. This recombination phenotype differs between female and male, and also among individuals of each gender. In this study, we used high-density SNP genotypes of over 2,
Externí odkaz:
https://doaj.org/article/3d41d96f680e47f4af4ec6de1c084ffc
Autor:
Albert Lai, Timothy F. Cloughesy, William H. Yong, Phioanh L. Nghiemphu, Paul S. Mischel, Linda M. Liau, Robert Prins, Horacio Soto, Jean Reiss, Weidong Chen, Jerry J. Lou, Reema R. Mody, Tie Li, Arthur P. Chou, Fei Liu, Reshmi Chowdhury, Sichen Li
Purpose:IDH1/2-mutant gliomas harbor a distinct glioma-CpG island methylation phenotype (G-CIMP) that may promote the initiation and progression of secondary pathway gliomas by silencing tumor-suppressive genes. The potential role of tumor-suppressiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87cd711dff9b76e81c4c32e5050b7da9
https://doi.org/10.1158/1078-0432.c.6523713
https://doi.org/10.1158/1078-0432.c.6523713
Autor:
Albert Lai, Timothy F. Cloughesy, William H. Yong, Phioanh L. Nghiemphu, Paul S. Mischel, Linda M. Liau, Robert Prins, Horacio Soto, Jean Reiss, Weidong Chen, Jerry J. Lou, Reema R. Mody, Tie Li, Arthur P. Chou, Fei Liu, Reshmi Chowdhury, Sichen Li
Supplemental Figures Legend
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9971bb1d9fca2455428d7ac27104973
https://doi.org/10.1158/1078-0432.22457835
https://doi.org/10.1158/1078-0432.22457835
Autor:
Albert Lai, Timothy F. Cloughesy, William H. Yong, Phioanh L. Nghiemphu, Paul S. Mischel, Linda M. Liau, Robert Prins, Horacio Soto, Jean Reiss, Weidong Chen, Jerry J. Lou, Reema R. Mody, Tie Li, Arthur P. Chou, Fei Liu, Reshmi Chowdhury, Sichen Li
Supplementary Figures S1-10. Figure S1. RRBS methylation results of full miR-148a-associated CpG island. Figure S2. The methylation status of IDH1 mutation is prognostic in GBM and Anaplastic Astrocytoma (Grade III). Figure S3. miR-148a promotor CpG
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38a809342c53d329dfd41a7c49f6afa7
https://doi.org/10.1158/1078-0432.22457841
https://doi.org/10.1158/1078-0432.22457841
Autor:
Albert Lai, Timothy F. Cloughesy, William H. Yong, Phioanh L. Nghiemphu, Paul S. Mischel, Linda M. Liau, Robert Prins, Horacio Soto, Jean Reiss, Weidong Chen, Jerry J. Lou, Reema R. Mody, Tie Li, Arthur P. Chou, Fei Liu, Reshmi Chowdhury, Sichen Li
Supplementary Tables S1-11. Supplementary Table S1. Patient demographics of the RRBS discovery set. Supplementary Table S2. RRBS Mean Coverage per sample. Supplementary Table S3. RRBS coverage of CpG islands associated with miRNAs. Supplementary Tabl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8358ca7ce68c59b74b95f302757c9c14
https://doi.org/10.1158/1078-0432.22457838
https://doi.org/10.1158/1078-0432.22457838
Publikováno v:
G3: Genes, Genomes, Genetics, Vol 6, Iss 12, Pp 3995-4007 (2016)
G3: Genes|Genomes|Genetics
G3: Genes|Genomes|Genetics
Meiotic recombination is an essential step in gametogenesis, and is one that also generates genetic diversity. Genome-wide association studies (GWAS) and molecular studies have identified genes that influence of human meiotic recombination. RNF212 is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5d653cd66bdc06dd90c896408a96352
https://doi.org/10.1534/g3.116.035766
https://doi.org/10.1534/g3.116.035766
Autor:
Albert Lai, Linda M. Liau, Yvonne T. Bui, Reshmi Chowdhury, Nhung T Nguyen, Tie Li, Timothy F. Cloughesy, Phioanh L. Nghiemphu, Byram Ozer, William H. Yong
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3067b6d78f8ee107f277d52b3081dbb
https://europepmc.org/articles/PMC5692108/
https://europepmc.org/articles/PMC5692108/
Autor:
Anh Tran, Reshmi Chowdhury, Weidong Chen, William H. Yong, Albert Lai, Whitney B. Pope, Arthur P. Chou, Desiree Sanchez, Phioanh L. Nghiemphu, Jonathan Lalezari, Ryan W. Wilson, Timothy F. Cloughesy, Robert Elashoff, Benjamin M. Ellingson, Shadi Lalezari, Mira Zurayk, Jerry J. Lou, Jose Carrillo, Karen Ancheta, Laurel Ormiston, Linda M. Liau, Paul S. Mischel, Richard M. Green, Robert Hanna, Sichen Li, Paul D. Miller, Colin Buchanan, He-Jing Wang, Negar Khanlou, Julia Selfridge, Orestes E. Solis, David Piccioni
Publikováno v:
Neuro-oncology, vol 15, iss 3
Glioblastoma multiforme (GBM) is the most common malignant primary brain tumor in adults. Current standard treatment for GBM includes cyto-reductive surgery followed by radiation (RT) and chemotherapy with temozolomide (TMZ).1 CpG methylation of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07c3717b7b6c2a6c23b85c4af8163042
https://doi.org/10.1093/neuonc/nos308
https://doi.org/10.1093/neuonc/nos308