Prasad Megana K - Division of Endocrinology, Diabetes and Nutrition, University of Maryland School of Medicine

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论文共 37 篇作者统计合作学者相似作者

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Beyond the Promise: Evaluating and Mitigating Off-Target Effects in CRISPR Gene Editing for Safer Therapeutics

Rui Lopes,Megana K. Prasad

Frontiers in bioengineering and biotechnology（2024）

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Generation and Characterization of a Fc.R-Humanized HFCGR2-3 Mice Line

Cristina Bertinetti-Lapatki, Kerstin Hahn, Martina Stirn,Felix Weber,Elisabeth Husar, Michael Gertz,Francois Christen,Megana Prasad,Roland Schmucki,Antonio Iglesias

INTERNATIONAL JOURNAL OF TOXICOLOGYno. 1 (2024): 98-99

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Multi-level characterization of the hypoxic stress response in retinal pigment epithelial cells

Lisa Gronnert,Juliane Siebourg-Polster,Florian Peters, Desiree von Tell,David Avila,Roland Schmucki,Megana Prasad,Manuel Tzouros,Javier Gayan,Peter Westenskow

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCEno. 8 (2023)

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A Simple, Quick, and Partially Automated Protocol for the Isolation of Single Nuclei from Frozen Mammalian Tissues for Single Nucleus Sequencing

Lucas Stalder, Fabian Koechl,Kerstin Hahn,Marc Sultan,Megana K Prasad

Journal of visualized experiments JoVE (2023)

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Multi-omics Based Metabolic Profiling of the Retinal Pigment Epithelium

Lisa Groennert,David Avila,Juliane Siebourg-Polster, Fabian Koechl,Manuel Tzouros,Megana Prasad,Javier Gayan,Peter Westenskow

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE（2021）

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Alzheimer's Risk Gene TREM2 Determines Functional Properties of New Type of Human Ipsc-Derived Microglia

Marvin Reich,Inaki Paris,Martin Ebeling,Nadine Dahm,Christophe Schweitzer,Dieter Reinhardt,Roland Schmucki,Megana Prasad,Fabian Kochl,Marcel Leist,Sally A. Cowley,Jitao David Zhang,Christoph Patsch,Simon Gutbier,Markus Britschgi

FRONTIERS IN IMMUNOLOGY（2021）

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Allele-specific Enhancers Mediate Associations Between LCAT and ABCA1 Polymorphisms and HDL Metabolism

Alicia D. Howard,Xiaochun Wang,Megana Prasad,Avinash Das Sahu,Radhouane Aniba,Michael Miller,Sridhar Hannenhalli,Yen-Pei Christy Chang

PloS one（2019）

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Protocol GenoDENT: Implementation of a New NGS Panel for Molecular Diagnosis of Genetic Disorders with Orodental Involvement

Tristan Rey,Julien Tarabeux,Bénédicte Gerard, Marion Delbarre,Antony Le Béchec,Corinne Stoetzel,Megana Prasad,Virginie Laugel-Haushalter,Marzena Kawczynski,Jean Muller,Jamel Chelly,Hélène Dollfus,Marie-Cécile Manière,Agnès Bloch-Zupan

Methods Mol. Biol.（2019）

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GenoDENT: A targeted next-generation sequencing assay for the molecular diagnosis of genetic disorders with orodental involvement

A. Bloch-Zupan, T. Rey,V. Laugel-Haushalter,C. Stoetzel,M. Prasad, M. Kawczynski, S. Troester,J. Muller,H. Dollfus,B. Gerard,J. Chelly

EUROPEAN JOURNAL OF HUMAN GENETICS（2019）

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Expanding Phenotype of Hereditary Fibrosing Poikiloderma with Tendon Contractures, Myopathy, and Pulmonary Fibrosis Caused by FAM111B Mutations: Report of an Additional Family Raising the Question of Cancer Predisposition and a Short Review of Early-Onset Poikiloderma

Raphaëlle Goussot,Megana Prasad,Corinne Stoetzel,Cédric Lenormand,Hélène Dollfus,Dan Lipsker

JAAD case reports（2017）

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