Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Davoud Mohtat"'
Autor:
Amit Verma, Katalin Susztak, John M. Greally, X. Shirley Liu, James Pullman, Masako Suzuki, Tushar D. Bhagat, Kristin Ware, Krishna Gundabolu, Nishanth Vallumsetla, Orsolya Giricz, Ae Seo Deok Park, Maria C. Izquierdo, Sanchari Bhattacharya, Niraj Shenoy, Yi-An Ko, Yiting Yu, Davoud Mohtat, Caroline Y. Hu
Purpose: Even though recent studies have shown that genetic changes at enhancers can influence carcinogenesis, most methylomic studies have focused on changes at promoters. We used renal cell carcinoma (RCC), an incurable malignancy associated with m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e66e795e1c48e44cfc7532f583ba641
https://doi.org/10.1158/1078-0432.c.6523062
https://doi.org/10.1158/1078-0432.c.6523062
Autor:
Amit Verma, Katalin Susztak, John M. Greally, X. Shirley Liu, James Pullman, Masako Suzuki, Tushar D. Bhagat, Kristin Ware, Krishna Gundabolu, Nishanth Vallumsetla, Orsolya Giricz, Ae Seo Deok Park, Maria C. Izquierdo, Sanchari Bhattacharya, Niraj Shenoy, Yi-An Ko, Yiting Yu, Davoud Mohtat, Caroline Y. Hu
PDF file - 77K, Supplementary Table 1: Clinical and Pathological characteristics of tumor samples. Supplementary Table 2: Aberrantly methylated and underexpressed loci with overlapping enhancer (H3K4me1) marks. Supplementary Table 3: Transcription fa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30afd016a9c5445ee5e15efc1e80da62
https://doi.org/10.1158/1078-0432.22455594
https://doi.org/10.1158/1078-0432.22455594
Autor:
Gayathri Menon, Christopher B. Pierce, Derek K. Ng, Sahar Fathallah-Shaykh, Anjali Nayak, Martin Turman, Tom Blydt-Hansen, Cynthia Wong, Steve Alexander, Ora Yadin, Elizabeth Ingulli, Robert Mak, Cheryl Sanchez-Kazi, Asha Moudgil, Samina Muneeruddin, Carolyn Abitbol, Marissa DeFrietas, Chryso Katsoufis, Wacharee Seeherunvong, Larry Greenbaum, Lyndsay Harshman, Priya Verghese, Sonia Krishnan, Amy Wilson, Stefan Kiessling, Siddharth Shah, Janice Sullivan, Sushil Gupta, Samir El-Dahr, Stacy Drury, Nancy Rodig, Allison Dart, Meredith Atkinson, Arlene Gerson, Tej Matoo, Zubin Modi, Jason Thomas, Bradley Warady, Rebecca Johnson, Vikas Dharnidharka, Stephen Hooper, Susan Massengill, Liliana Gomez-Mendez, Matthew Hand, Joann Carlson, Craig Wong, Frederick Kaskel, Shlomo Shinnar, Jeffrey Saland, Marc Lande, George Schwartz, Anil Mongia, Donna Claes, Mark Mitsnefes, Katherine Dell, Hiren Patel, Pascale Lane, Rulan Parekh, Lisa Robinson, Amira Al-Uzri, Kelsey Richardson, Susan Furth, Larry Copelovitch, Elaine Ku, Joshua Samuels, Poyyapakkam Srivaths, Samhar Al-Akash, Davoud Mohtat, Victoria Norwood, Joseph Flynn, Cynthia Pan, Sharon Bartosh
Publikováno v:
American journal of kidney diseases : the official journal of the National Kidney Foundation.
Autor:
Yi-An Ko, Kristin Ware, X. Shirley Liu, Orsolya Giricz, Sanchari Bhattacharya, Yiting Yu, Caroline Hu, Krishna Gundabolu, Ae Seo Deok Park, John M. Greally, Nishanth Vallumsetla, Katalin Susztak, James Pullman, Amit Verma, María Concepción Izquierdo, Masako Suzuki, Davoud Mohtat, Niraj Shenoy, Tushar D. Bhagat
Publikováno v:
Clinical Cancer Research. 20:4349-4360
Purpose: Even though recent studies have shown that genetic changes at enhancers can influence carcinogenesis, most methylomic studies have focused on changes at promoters. We used renal cell carcinoma (RCC), an incurable malignancy associated with m
Autor:
James Pullman, Katalin Susztak, Ae Seo Deok Park, Davoud Mohtat, Karolina Woroniecka, David B. Thomas
Publikováno v:
Diabetes
OBJECTIVE Diabetic kidney disease (DKD) is the single leading cause of kidney failure in the U.S., for which a cure has not yet been found. The aim of our study was to provide an unbiased catalog of gene-expression changes in human diabetic kidney bi
Autor:
Thomas Moulton, Rosemary Thomas, Yaa Boakye, Davoud Mohtat, Catherine Driscoll, Robert P. Woroniecki, Zangfang Du
Publikováno v:
Pediatric Nephrology. 26:275-280
Renal dysfunction affects 5–18% of patients with sickle cell disease (SCD). To date, no studies have described urinary levels of transforming growth factor β-1 (TGF-β1), a marker of fibrosis, and neutrophil gelatinase-associated lipocalin (NGAL),
Autor:
Davoud Mohtat, Katalin Susztak
Publikováno v:
Seminars in Nephrology. 30:468-476
An epigenetic trait is a stably inherited phenotype resulting from changes in a chromosome without alterations in the DNA sequence. Epigenetic modifications such as DNA methylation, together with covalent modification of histones, are thought to alte
Autor:
Micki McCollister, Julie Hevezi, Naomi Santoni, Tracey Tam, Rajesh Pahwa, Cynthia Alcorn-Costa, Barbara Fussell, Xiaoming Lu, Cheryl Armstrong, Peggy Gray, Patricia Dyches, Jovianna N. Wellinghoff, Shaunna Caouette, James B. Osborne, William C. Koller, Tilak Mendis, Shantelle Coe, Jacqueline Nash, Shirley Uy, Howard I. Hurtig, Susan Rolli, Tracy Stewart, Judy Richman, Susan Rolandelli, William G. Ondo, Cathi A. Thomas, Melodie Moterson, Maryan DeAngelis, Sheila Everett, Mary Mathews, Linda L. Mann, Eric Molho, Lorette J. Jenkins, Jessie Roth, Sandra K. Kostyk, Deborah L. Caputo, Ali H. Rajput, Jean Ayan, Un Jung Kang, Paul Atchison, Jo Belden, Julie So, Andew Feigin, Lisa Johnston, Lawrence I. Golb, Howard H. Hurtig, Larisa I. Skrypnik, Michael J. Aminoff, J. Carpenter, Patricia Seuffert, Carlos Singer, Amy Parsons, Kapil D. Sethi, Mark Forrest Gordon, Pam King, Mary Lloyd, Katherine B. Hawthorne, Linda Klassen, Shoba Narayan, Cathy R. Anderson, Patricia Kaminski, Karen Caplan, Robert A. Hauser, Dinorah Bateman, Erica Barnabei, Cheryl Fitzer-Attas, Kellie Gelles, Tamara Gales, Joanne Wojcieszek, Robert Hauser, Teri Radam, Karen Stavris, Carolyn C. Weeks, Marlene Gerow, Connie Kawai, Tracey Borst, Caroline M. Tanner, Charles H. Adler, Mickie Welsh, Nancy Pearson, Anita Lopez, Georgia Germain, Cathy W. Allen, Marianne Ewasnishin, Lisa Tagg, Brenda Ebbitt, Myrna Schear, Jean A. Jaglin, Roberta Winnick, Dawn Miller, Nancy Saton, Suzanne W. Schuman, Davoud Mohtat, Barbara Shannon, Vincent Calabrese, Mark F. Lew, Janis M. Miyasaki, William J. Weiner, Jody Lowery, Christine Hunter, Diane Brown, Keely Haas, Paul J. Tuite, Peter A. LeWitt, Mirann DiMinno, Cheryl Cooper, Peter Novak, Robert G. Feldman, Joanne Hamann, Sharon Evans, W.R. Wayne Martin, Mark Stacy, Debra Berry, Sharon Wortzel, John M. Bertoni, Kenneth Marek, Kelli Williamson, Lisa Gauger, Cheryl Newcomb, Carolyn Peterson, K. Ligon, Stephanie Newman, Vanessa Patterson, Peggy Roberge, Arif Dalvi, Laura Sutherland, Frederick J. Marshall, Scott Cradr, Karen Betcher, Carolyn Deloa, Jean P. Hubble, Kathleen M. Shannon, Sharyn Parness, Neila Mendis, Germanine McInnes, Adrienne Baranauskas, Irenita Gardiner
Publikováno v:
Movement disorders : official journal of the Movement Disorder Society. 24(4)
The purpose of this study to compare the long-term clinical outcome of early versus delayed rasagiline treatment in early Parkinson's disease (PD). Subjects (N = 404) were randomly assigned to initial treatment with rasagiline (early-start group) or
Autor:
James Pullman, Tushar D. Bhagat, Katalin Susztak, Yan Yu, K. Ware, Amit Verma, A. Ari Hakimi, Reza Ghavamian, Christoph Heuck, Davoud Mohtat, Caroline Hu
Publikováno v:
Journal of Clinical Oncology. 29:e15000-e15000
e15000 Background: Metastatic renal cell carcinoma (RCC) has a very poor prognosis with limited therapeutic options. Despite this, there have been very few global genetic and epigenetic studies of ...
Publikováno v:
Blood. 114:4621-4621
Abstract 4621 Renal failure is one of the major complications of sickle cell disease (SCD), affecting 5-18% of the patients. Microalbuminuria (MA), which has a prevalence of 26.5% in all children with SCD, is used as a marker of preclinical glomerula