Хайлтын үр дүнгүүд - Samarth Bhatt
- 15-н 1 - 15 үр дүнгүүдийг харуулж байна
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Prenatal Maternal Stress Predicts Methylation of Genes Regulating the Hypothalamic–Pituitary–Adrenocortical System in Mothers and Newborns in the Democratic Republic of Congo -н Darlene A. Kertes, Hayley S. Kamin, David A. Hughes, Nicole C Rodney, Samarth Bhatt, Connie J. Mulligan
Хэвлэсэн 2016Artigo -
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An unusual T-cell childhood acute lymphoblastic leukemia harboring a yet unreported near-tetraploid karyotype -н Daniela R. Ney Garcia, Samarth Bhatt, Marina Manvelyan, Mariana Tavares de Souza, Renata Binato, Thais Ferraz Aguiar, Eliana Abdelhay, Maria Luíza M. Silva
Хэвлэсэн 2011Artigo -
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Human Ring Chromosomes – New Insights for their Clinical Significance -н Roberta Santos Guilherme, Elisabeth Klein, Ahmed B. Hamid, Samarth Bhatt, Marianne Volleth, A. Polityko, Anna Kulpanovich, Andreas Dufke, Beate Albrecht, Susanne Morlot, Lukrecija Brečević, Michael B. Petersen, Emmanouil Manolakos, Nadezda Kosyakova, Thomas Liehr
Хэвлэсэн 2013Artigo -
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Chromosomes in a genome-wise order: evidence for metaphase architecture -н Anja Weise, Samarth Bhatt, Katja Piaszinski, Nadezda Kosyakova, Xiaobo Fan, A. Altendorf-Hofmann, Alongklod Tanomtong, Arunrat Chaveerach, Marcelo de Bello Cioffi, Edivaldo Herculano Corrêa de Oliveira, Joachim-U. Walther, Thomas Liehr, J. P. Chaudhuri
Хэвлэсэн 2016Artigo -
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A small recurrent deletion within 15q13.3 is associated with a range of neurodevelopmental phenotypes -н Marwan Shinawi, Christian P. Schaaf, Samarth Bhatt, Zhilian Xia, Ankita Patel, Sau Wai Cheung, Brendan C. Lanpher, Sandra Nagl, Heinrich Stephan Herding, Claudia Nevinny-Stickel, LaDonna Immken, Gayle Patel, Jennifer R. German, Arthur L. Beaudet, Paweł Stankiewicz
Хэвлэсэн 2009Artigo -
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Rare pathogenic microdeletions and tandem duplications are microhomology-mediated and stimulated by local genomic architecture -н Lisenka E.L.M. Vissers, Samarth Bhatt, Irene M. Janssen, Zhilian Xia, Seema R. Lalani, Rolph Pfundt, Katarzyna Derwińska, Bert B.A. de Vries, Christian Gilissen, Alexander Hoischen, Monika Nesteruk, Barbara Wiśniowiecka‐Kowalnik, Marta Smyk, Han G. Brunner, Sau Wai Cheung, Ad Geurts van Kessel, Joris A. Veltman, Paweł Stankiewicz
Хэвлэсэн 2009Artigo -
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Insights into Sex Chromosome Evolution and Aging from the Genome of a Short-Lived Fish -н Kathrin Reichwald, A. Petzold, Philipp Koch, Bryan Downie, Nils Hartmann, Stefan Pietsch, Mario Baumgart, Domitille Chalopin, Marius Felder, Martin Bens, Arne Sahm, Karol Szafranski, Stefan Taudien, Marco Groth, Ivan Arisi, Anja Weise, Samarth Bhatt, Virag Sharma, Johann M. Kraus, Florian Schmid, Stefan Priebe, Thomas Liehr, Matthias Görlach, Manuel E. Than, Michael Hiller, Hans A. Kestler, Jean‐Nicolas Volff, Manfred Schartl, Alessandro Cellerino, Christoph Englert, Matthias Platzer
Хэвлэсэн 2015Artigo -
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Heteromorphic variants of chromosome 9 -н Nadezda Kosyakova, Ani Grigorian, Thomas Liehr, Marina Manvelyan, Isabella Simonyan, Hasmik Mkrtchyan, Rouben Aroutiounian, A. Polityko, Anna Kulpanovich, Tatiana Egorova, Evgenia Jaroshevich, Alla Frolova, Natalia Shorokh, И.В. Наумчик, Marianne Volleth, Isolde Schreyer, Heike Nelle, Markus Stümm, Rolf‐Dieter Wegner, Gisela Reising-Ackermann, Martina Merkaš, Lukretija Brecevic, T. John Martin, Laura Rodríguez, Samarth Bhatt, Monika Ziegler, Katharina Kreskowski, Anja Weise, Ali Sazcı, Svetlana G. Vorsanova, Marcelo de Bello Cioffi, Emel Ergül
Хэвлэсэн 2013Artigo -
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Genomic and Genic Deletions of the FOX Gene Cluster on 16q24.1 and Inactivating Mutations of FOXF1 Cause Alveolar Capillary Dysplasia and Other Malformations -н Paweł Stankiewicz, Partha Sen, Samarth Bhatt, Mekayla A. Storer, Zhilian Xia, Bassem A. Bejjani, Zhishuo Ou, Joanna Wiszniewska, Daniel J. Driscoll, Juan M. Bolívar, Mislen Bauer, Elaine H. Zackai, Donna M. McDonald‐McGinn, Małgorzata M.J. Nowaczyk, Mitzi L. Murray, Tamim H. Shaikh, Vicki Martin, Matthew Tyreman, Ingrid Simonic, Lionel Willatt, Joan Paterson, Sarju Mehta, Diana Rajan, Tomas Fitzgerald, Susan Gribble, Elena Prigmore, Ankita Patel, Lisa G. Shaffer, Nigel P. Carter, Sau Wai Cheung, Claire Langston, Charles Shaw‐Smith
Хэвлэсэн 2009Artigo -
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Genomic and Genic Deletions of the FOX Gene Cluster on 16q24.1 and Inactivating Mutations of FOXF1 Cause Alveolar Capillary Dysplasia and Other Malformations -н Paweł Stankiewicz, Partha Sen, Samarth Bhatt, Mekayla A. Storer, Zhilian Xia, Bassem A. Bejjani, Zhishuo Ou, Joanna Wiszniewska, Daniel J. Driscoll, Melissa K. Maisenbacher, Juan M. Bolívar, Mislen Bauer, Elaine H. Zackai, Donna M. McDonald‐McGinn, Małgorzata M.J. Nowaczyk, Mitzi L. Murray, Virginia A. Hustead, Kristin Mascotti, Regina Schultz, Lavinia Hallam, D. Harold McRae, Andrew G. Nicholson, Robert Newbury, Jane Durham-O'Donnell, G. R. Knight, Usha Kini, Tamim H. Shaikh, Vicki Martin, Matthew Tyreman, Ingrid Simonic, Lionel Willatt, Joan Paterson, Sarju Mehta, C. Jones, Diana Rajan, Tomas Fitzgerald, Susan Gribble, Elena Prigmore, Ankita Patel, Lisa G. Shaffer, Nigel P. Carter, Sau Wai Cheung, Claire Langston, Charles Shaw‐Smith
Хэвлэсэн 2009Artigo -
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Recurrent deletions and reciprocal duplications of 10q11.21q11.23 including CHAT and SLC18A3 are likely mediated by complex low-copy repeats -н Paweł Stankiewicz, Shashikant Kulkarni, Avinash V. Dharmadhikari, Srirangan Sampath, Samarth Bhatt, Tamim H. Shaikh, Zhilian Xia, Amber N. Pursley, M. Lance Cooper, Marwan Shinawi, Alex R. Paciorkowski, Dorothy K. Grange, Michael J. Noetzel, Scott Saunders, Paul Simons, Marshall Summar, Brendan Lee, Fernando Scaglia, Florence Fellmann, Danielle Martinet, J. Beckmann, Alexander Asamoah, Kathryn Platky, Susan Sparks, Ann Martin, Suneeta Madan‐Khetarpal, Jacqueline M. Hoover, Līvija Medne, Carsten G. Bönnemann, John B. Moeschler, Stephanie E. Vallee, Sumit Parikh, Polly Irwin, Victoria P. Dalzell, Wendy E. Smith, Valerie Banks, David B. Flannery, Carolyn Lovell, Gary A. Bellus, Kathryn Golden-Grant, Jerome L. Gorski, Jennifer Kussmann, Tracy L. McGregor, Rizwan Hamid, Jean P. Pfotenhauer, Blake C. Ballif, Chad A. Shaw, Sung‐Hae Kang, Carlos A. Bacino, Ankita Patel, Jill A. Rosenfeld, Sau Wai Cheung, Lisa G. Shaffer
Хэвлэсэн 2011Artigo
Хайх хэрэгслүүд:
Холбогдох сэдвүүд
Gene
Biology
Genetics
Chromosome
Genome
Computational biology
Human genetics
Phenotype
Copy-number variation
Epigenetics
Gene duplication
Internal medicine
Karyotype
Medicine
Pregnancy
Chemistry
Comparative genomic hybridization
Cytogenetics
DNA methylation
Endocrinology
Evolutionary biology
Fish <Actinopterygii>
Fishery
Frameshift mutation
Gene expression
Gene family
Genetic recombination
Haploinsufficiency
Methylation
Non-allelic homologous recombination