Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Manjunath Nimmakayalu"'
Autor:
Raefa Abou Khouzam, Shyama Prasad Rao, Goutham Hassan Venkatesh, Nagwa Ahmed Zeinelabdin, Stephanie Buart, Maxime Meylan, Manjunath Nimmakayalu, Stéphane Terry, Salem Chouaib
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
Intratumoral hypoxia is a widely established element of the pancreatic tumor microenvironment (TME) promoting immune escape, tumor invasion, and progression, while contributing to treatment resistance and poor survival. Despite this critical role, hy
Externí odkaz:
https://doaj.org/article/99d054e25d7a4785a970ece341958414
Publikováno v:
BioTechniques, Vol 28, Iss 3, Pp 518-522 (2000)
Many projects, such as multiplex-fluorescence in situ hybridization (M-FISH) karyotyping, require the use of relatively large amounts of multiple fluor- or hapten-labeled nucleotides for the preparation of DNA probes. Such a requirement makes these e
Externí odkaz:
https://doaj.org/article/d4f1ce01604042ab9f46fdc372ccc3c8
Autor:
Hui Yang, Guillermo Garcia-Manero, Koji Sasaki, Guillermo Montalban-Bravo, Zhenya Tang, Yue Wei, Tapan Kadia, Kelly Chien, Diana Rush, Ha Nguyen, Awdesh Kalia, Manjunath Nimmakayalu, Carlos Bueso-Ramos, Hagop Kantarjian, L. Jeffrey Medeiros, Rajyalakshmi Luthra, Rashmi Kanagal-Shamanna
Publikováno v:
Leukemia. 36:2306-2316
Chromosome banding analysis (CBA) remains the standard-of-care for structural variant (SV) assessment in MDS. Optical genome mapping (OGM) is a novel, non-sequencing-based technique for high-resolution genome-wide SV profiling (SVP). We explored the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::829fbce5230bebc423aa6a411f28b525
https://doi.org/10.1038/s41375-022-01652-8
https://doi.org/10.1038/s41375-022-01652-8
Autor:
Dmitry A. Gordenin, Jesse R. Dixon, Sarah Killcoyne, Erica Lynn, Peter J. Campbell, Manjunath Nimmakayalu, Rebecca C. Fitzgerald, Yanyan Tian, Sahil Seth, Yonathan Lissanu Deribe, John P. O'Brien, Akira Inoue, Victoria T. Le, Roel G.W. Verhaak, Kadir C. Akdemir, Leszek J. Klimczak, Moritz Gerstung, Rafael E. Herrera, Ya-Ping Lin, Lei Li, Justin M. Kim, Samirkumar B. Amin, P. Andrew Futreal, Frederick S. Robinson, Kin Chan, Ashby J. Morrison, Devin A. King
Publikováno v:
Nat Genet
Somatic mutations in driver genes may ultimately lead to the development of cancer. Understanding how somatic mutations accumulate in cancer genomes and the underlying factors that generate somatic mutations is therefore crucial for developing novel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1818b109cb8ef8b8d489419624301e0d
https://doi.org/10.1038/s41588-020-0708-0
https://doi.org/10.1038/s41588-020-0708-0
Autor:
Diana Marcela Rush, Rajyalakshmi Luthra, Peter Hu, Carlos Bueso-Ramos, Manjunath Nimmakayalu, Zhenya Tang, Keyur Patel, Francis San Lucas, James Ozenci, Simi Puthooran, L. Jeffrey Medeiros, Bedia Barkoh, Sherin Raju, Nazneen Ahmed, Rashmi Kanagal-Shamanna
Publikováno v:
Cancer Genetics. :16-17
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9107748a1bd02cedad22e6216830c305
https://doi.org/10.1016/j.cancergen.2021.05.063
https://doi.org/10.1016/j.cancergen.2021.05.063
Autor:
Stéphane Terry, Shyama Prasad Rao, Stéphanie Buart, Maxime Meylan, Manjunath Nimmakayalu, Nagwa Ahmed Zeinelabdin, Salem Chouaib, Goutham Hassan Venkatesh, Raefa Abou Khouzam
Publikováno v:
Frontiers in Immunology
Frontiers in Immunology, Frontiers, 2021, 12, ⟨10.3389/fimmu.2021.680435⟩
Frontiers in Immunology, Vol 12 (2021)
Frontiers in Immunology, 2021, 12, ⟨10.3389/fimmu.2021.680435⟩
Frontiers in Immunology, Frontiers, 2021, 12, ⟨10.3389/fimmu.2021.680435⟩
Frontiers in Immunology, Vol 12 (2021)
Frontiers in Immunology, 2021, 12, ⟨10.3389/fimmu.2021.680435⟩
International audience; Intratumoral hypoxia is a widely established element of the pancreatic tumor microenvironment (TME) promoting immune escape, tumor invasion, and progression, while contributing to treatment resistance and poor survival. Despit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83cdf23486aa140ce98b3afa5f612110
https://hal.sorbonne-universite.fr/hal-03253996
https://hal.sorbonne-universite.fr/hal-03253996
Autor:
Guillermo Garcia-Manero, Zhenya Tang, Kelly S. Chien, Awdesh Kalia, Diana Rush, Hagop M. Kantarjian, Yue Wei, Rashmi Kanagal-Shamanna, Manjunath Nimmakayalu, Rajyalakshmi Luthra, Hui Yang, L. Jeffrey Medeiros, Saradhi Mallampati, Guillermo Montalban-Bravo
Publikováno v:
Blood. 138:105-105
Introduction Introduction of next-generation sequencing has defined the somatic mutational landscape in MDS. Comprehensive high-throughput structural variant profiling (SVP) is as important as mutation profiling in characterizing MDS clonal architect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::98670969445566a52aef373a21295e41
https://doi.org/10.1182/blood-2021-154005
https://doi.org/10.1182/blood-2021-154005
Autor:
Shivanand R. Patil, Susannah Q. Longmuir, Kim M. Keppler-Noreuil, Andrew B. Cyr, Oleg A. Shchelochkov, Manjunath Nimmakayalu
Publikováno v:
American Journal of Medical Genetics Part A. 155:2224-2228
Larger imbalances on chromosome 4p in the form of deletions associated with Wolf-Hirschhorn syndrome (WHS) and duplications of chromosome 4p have a defined clinical phenotype. The critical region for both these clinical disorders has been narrowed ba
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab23182e31cf4c45ae2061a57f1074ee
https://doi.org/10.1002/ajmg.a.34120
https://doi.org/10.1002/ajmg.a.34120
Autor:
Tian Xu, Jingwei Yu, Barbara R. Pober, Manjunath Nimmakayalu, Peining Li, Shannon Huff, Mazin B. Qumsiyeh, Hui Z. Zhang, Anna Szekely
Publikováno v:
American Journal of Medical Genetics Part A. :2721-2729
We detected a unique de novo complex chromosome rearrangement (CCR) in a patient with multiple abnormalities including growth retardation, facial anomalies, exudative vitreoretinopathy (EVR), cleft palate, and minor digital anomalies. Cytogenetic ana
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74ced9f9243a5cb2d6962dedb46e180b
https://doi.org/10.1002/ajmg.a.31498
https://doi.org/10.1002/ajmg.a.31498
Autor:
Manjunath Nimmakayalu, Hui Z. Zhang, Mazin B. Qumsiyeh, Barbara R. Pober, Peining Li, Shannon Huff, Dongmei Wang
Publikováno v:
American Journal of Medical Genetics. :280-287
We report a case of ring chromosome 6 presenting with growth and mental retardation, cerebral dysgenesis, eye malformations, mixed hearing loss, and abnormal physical features. Fluorescent in situ hybridization (FISH) and microsatellite genotyping de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1125a99a0ce76af05aeb7a35e3a561e8
https://doi.org/10.1002/ajmg.a.20413
https://doi.org/10.1002/ajmg.a.20413