Výsledky vyhledávání - Anshika Srivastava
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Most frequent South Asian haplotypes of ACE2 share identity by descent with East Eurasian populations Autor Anshika Srivastava, Rudra Kumar Pandey, Prajjval Pratap Singh, Pramod Kumar, Avinash Arvind Rasalkar, Rakesh Tamang, George van Driem, Pankaj Shrivastava, Gyaneshwer Chaubey
Vydáno 2020Artigo -
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<i>De novo</i>dominant<i>ASXL3</i>mutations alter H2A deubiquitination and transcription in Bainbridge–Ropers syndrome Autor Anshika Srivastava, K.C. Ritesh, Yao-Chang Tsan, Rosy Liao, Fengyun Su, Xuhong Cao, Mark C. Hannibal, Catherine E. Keegan, Arul M. Chinnaiyan, Donna M. Martin, Stephanie Bielas
Vydáno 2015Artigo -
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Genetic analysis of CHARGE syndrome identifies overlapping molecular biology Autor Amanda Moccia, Anshika Srivastava, Jennifer Skidmore, John Bernat, Marsha M. Wheeler, Jessica X. Chong, Deborah A. Nickerson, Michael J. Bamshad, Margaret A. Hefner, Donna M. Martin, Stephanie Bielas
Vydáno 2018Artigo -
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Genetic Association of ACE2 rs2285666 Polymorphism With COVID-19 Spatial Distribution in India Autor Anshika Srivastava, Audditiya Bandopadhyay, Debashruti Das, Rudra Kumar Pandey, Vanya Singh, Nargis Khanam, Nikhil Srivastava, Prajjval Pratap Singh, Pavan Kumar Dubey, Abhishek Pathak, Pranav Gupta, Niraj Rai, Gazi Nurun Nahar Sultana, Gyaneshwer Chaubey
Vydáno 2020Artigo -
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Photosensitivity and type I IFN responses in cutaneous lupus are driven by epidermal-derived interferon kappa Autor Mrinal K. Sarkar, Grace A. Hile, Lam C. Tsoi, Xianying Xing, Jianhua Liu, Yun Liang, Céline C. Berthier, William R. Swindell, Matthew T. Patrick, Shuai Shao, Pei‐Suen Tsou, Ranjitha Uppala, Maria A. Beamer, Anshika Srivastava, Stephanie Bielas, Paul W. Harms, Spiro Getsios, James T. Elder, John J. Voorhees, Jóhann E. Guðjónsson, J. Michelle Kahlenberg
Vydáno 2018Artigo -
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Genotype-phenotype correlations in individuals with pathogenic<i>RERE</i>variants Autor Valerie K. Jordan, Brieana Fregeau, Xiaoyan Ge, Jessica L. Giordano, Ronald J. Wapner, Tuğçe B. Balcı, Jennefer N. Carter, John Bernat, Amanda Moccia, Anshika Srivastava, Donna M. Martin, Stephanie Bielas, John Pappas, Melissa Svoboda, Marlène Rio, Nathalie Boddaert, Vincent Cantagrel, Andrea M. Lewis, Fernando Scaglia, Jennefer N. Kohler, Jonathan A. Bernstein, Annika M. Dries, Jill A. Rosenfeld, Colette DeFilippo, Willa Thorson, Yaping Yang, Elliott H. Sherr, Weimin Bi, Daryl A. Scott
Vydáno 2018Artigo -
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Biallelic variants in CSMD1 are implicated in a neurodevelopmental disorder with intellectual disability and variable cortical malformations Autor Elizabeth A. Werren, Emily Peirent, Henna Jäntti, Alba Guxholli, Kinshuk Raj Srivastava, Naama Orenstein, Vinodh Narayanan, Wojciech Wiszniewski, Mateusz Dawidziuk, Paweł Gawliński, Muhammad Umair, Amjad Khan, Shahid Niaz Khan, David Geneviève, Daphné Lehalle, Koen L.I. van Gassen, Jacques C. Giltay, Renske Oegema, Richard H. van Jaarsveld, Rafiullah Rafiullah, Gudrun Rappold, Rachel Rabin, John Pappas, Marsha M. Wheeler, Michael J. Bamshad, Yao-Chang Tsan, Matthew B. Johnson, Catherine E. Keegan, Anshika Srivastava, Stephanie Bielas
Vydáno 2024Artigo
Vyhledávací nástroje:
Související témata
Biology
Genetics
Gene
Genotype
Disease
Evolutionary biology
Medicine
Pathology
Phenotype
Coronavirus disease 2019 (COVID-19)
Epigenetics
Haploinsufficiency
Haplotype
Infectious disease (medical specialty)
Phylogenetic tree
Population
2019-20 coronavirus outbreak
Anatomy
Antibody
Apoptosis
Archaeology
Atresia
Basigin
Biochemistry
CHARGE syndrome
Cell culture
Central nervous system
China
Choanal atresia
Chromatin