R
Riyad N.H. Seervai
Researcher at Baylor College of Medicine
Publications - 20
Citations - 202
Riyad N.H. Seervai is an academic researcher from Baylor College of Medicine. The author has contributed to research in topics: Medicine & Internal medicine. The author has an hindex of 5, co-authored 11 publications receiving 104 citations. Previous affiliations of Riyad N.H. Seervai include Brown University.
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Journal ArticleDOI
Comprehensive Molecular Characterization Identifies Distinct Genomic and Immune Hallmarks of Renal Medullary Carcinoma
Pavlos Msaouel,Pavlos Msaouel,Gabriel G. Malouf,Gabriel G. Malouf,Xiaoping Su,Hui Yao,Durga Nand Tripathi,Melinda Soeung,Jianjun Gao,Priya Rao,Cristian Coarfa,Chad J. Creighton,Chad J. Creighton,Jean-Philippe Bertocchio,Jean-Philippe Bertocchio,Selvi Kunnimalaiyaan,Asha S. Multani,Jorge Blando,Rong He,Daniel D. Shapiro,Luigi Perelli,Sanjana Srinivasan,Federica Carbone,Patrick G. Pilie,Menuka Karki,Riyad N.H. Seervai,Bujamin Hektor Vokshi,Bujamin Hektor Vokshi,Dolores Lopez-Terrada,Emily H. Cheng,Ximing Tang,Wei Lu,Ignacio I. Wistuba,Timothy C. Thompson,Irwin Davidson,Virginia Giuliani,Katharina Schlacher,Alessandro Carugo,Timothy P. Heffernan,Padmanee Sharma,Jose A. Karam,Christopher G. Wood,Cheryl L. Walker,Giannicola Genovese,Nizar M. Tannir +44 more
TL;DR: Comprehensive genomic and transcriptomic profiling of untreated primary RMC tissues found that RMC was characterized by high replication stress and an abundance of focal copy-number alterations associated with activation of the stimulator of the cyclic GMP-AMP synthase interferon genes (cGAS-STING) innate immune pathway.
Journal ArticleDOI
Parasexuality and Ploidy Change in Candida tropicalis
Riyad N.H. Seervai,Stephen K. Jones,Matthew P. Hirakawa,Allison M. Porman,Richard J. Bennett +4 more
TL;DR: These experiments demonstrate distinct pathways by which a parasexual cycle can occur in C. tropicalis and indicate that nonmeiotic mechanisms drive ploidy changes in this prevalent human pathogen.
Journal ArticleDOI
Lessons for inductive germline determination.
TL;DR: The hypothesis that the transition between these determination mechanisms is more of a continuum than a binary change is discussed, and an analogy between germline determination and sex determination in vertebrates—two of the milestones of reproduction and development—is proposed.
Journal ArticleDOI
The Huntingtin-interacting protein SETD2/HYPB is an actin lysine methyltransferase.
Riyad N.H. Seervai,Rahul K. Jangid,Menuka Karki,Durga Nand Tripathi,Sung Yun Jung,Sarah Kearns,Kristen J. Verhey,Michael A. Cianfrocco,Bryan A. Millis,Matthew J. Tyska,Frank M. Mason,W. Kimryn Rathmell,In Young Park,Ruhee Dere,Cheryl L. Walker +14 more
TL;DR: This work shows that SETD2 is an actin methyltransferase that trimethylates lysine-68 (ActK68me3) in cells via its interaction with HTT and the actin-binding adapter HIP1R and identifies it as a previously unknown HTT effector regulating methylation and polymerization of actin filaments.
Journal ArticleDOI
A cytoskeletal function for PBRM1 reading methylated microtubules
Menuka Karki,Rahul K. Jangid,Ramakrishnan Anish,Riyad N.H. Seervai,Jean-Philippe Bertocchio,Jean-Philippe Bertocchio,Takashi Hotta,Pavlos Msaouel,Sung Yun Jung,Sandra L. Grimm,Cristian Coarfa,Bernard E. Weissman,Ryoma Ohi,Kristen J. Verhey,H. Courtney Hodges,Warren W. Burggren,Ruhee Dere,In Young Park,B. V. Venkataram Prasad,W. Kimryn Rathmell,Cheryl L. Walker,Durga Nand Tripathi +21 more
TL;DR: In this paper, the authors show that the coordinated read-write activity of the epigenetic machinery extends to the cytoskeleton, with PBRM1 in the PBAF chromatin remodeling complex reading microtubule methyl marks written by the SETD2 histone methyltransferase.