Peter Pechan - Genetic Therapy , Inc;Novartis Company

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论文共 78 篇作者统计合作学者相似作者

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Data from sFLT01: A Novel Fusion Protein with Antiangiogenic Activity

Rebecca G. Bagley, Leslie Kurtzberg,William Weber,Tri-Hung Nguyen,Stephanie Roth,Roy Krumbholz,Min Yao, Brenda Richards,Mindy Zhang,Peter Pechan, Steve Schmid,Abraham Scaria,

crossref（2023）

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Continued In Vitro And In Vivo Characterization Of Novel Aav Vectors Engineered For Muscle Gene Delivery

Jennifer Green,Tiffany Willacy,Jessica Boehler, Alina Dhruva,Hui Meng,Margaret Beatka,Emily Ott, Mariah Prom,Michael W. Lawlor,Peter Pechan,Carl Morris

MOLECULAR THERAPY（2021）

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Detailed Protocol for the Novel and Scalable Viral Vector Upstream Process for AAV Gene Therapy Manufacturing

Nagarathinam Selvaraj, Chao-Kuei Wang, Brian Bowser, Trevor Broadt, Samir Shaban,Jenna Burns, Nirmala Saptharishi,Peter Pechan,Diane Golebiowski,Asaf Alimardanov,Nora Yang, George Mitra,

Human gene therapy（2021）

引用11浏览0WOS引用

Characterization of Novel AAV Vectors Engineered for Muscle Gene Delivery

Jennifer Green,Diane Golebiowski,Tiffany Willacy,Guanrong Huang,Meghan Soustek-Kramer, Paul Nguyen, Sara Anderson, Alena Hornakova,Sharon McGonigle,Carl Morris,Peter Pechan

MOLECULAR THERAPY（2020）

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Evaluation of rAAV vectors engineered for muscle gene delivery

P. Pechan, J. Green, T. Willacy, J. Boehler, L. Such, M. Soustek-Kramer,P. Nguyen,R. Huang, R. Reals, K. J. Brown, D. Golebiowski, C. Morris

HUMAN GENE THERAPY（2019）

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Characterization of HSV Derived AAV9 Vectors

Peter Pechan, Diane Golebiowski, Alexey Seregin, Nicole Zapata, Elise Levi, Christine Kitsos, Robert Lu, Alvaro Amorrortu, Carl Morris

MOLECULAR THERAPY（2019）

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Award Winner for Michael Conneally Genetics Abstract Selection of an Adeno-Associated Virus Gene Therapy Targeting Huntingtin for the Treatment of Huntington's Disease

Pengcheng Zhou,Fen Chen,Xin Wang,Emily Christensen,Jeff Thompson,Mathieu Nonnenmacher,Maria Scheel,Xiao Ren,Wei Wang,Xiaochuan Zhou,Lisa Stanek,Bryan Mastis,

NEUROTHERAPEUTICS（2018）

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Robust Huntingtin knockdown in cortex and putamen in large mammals using a novel dosing paradigm with VY-HTT01, an AAV gene therapy targeting Huntington for the treatment of Huntington's disease

P. Zhou,J. Carroll, F. Chen,J. Thompson,J. Aubin, E. Christensen,L. Liu,T. Nguyen,M. Scheel,P. Pechan, A. Kells, C. Gamba-Vitalo,

HUMAN GENE THERAPY（2018）

引用2浏览0引用

Safety and Increased Transduction Efficiency in the Adult Nonhuman Primate Central Nervous System with Intravenous Delivery of Two Novel Adeno-Associated Virus Capsids

Dinah Sah, Allyse Mazzarelli,Emily Christensen,Jeff Thompson, Holly Lindgren,Ada Felix-Ortiz, Justin Aubin,Maria Scheel,Peter Pechan,Eric Horowitz,Shamone Fine, Yanqun Shu,

MOLECULAR THERAPY（2018）

引用5浏览0引用

Pharmacology and Safety of VY-HTT01, an AAV miRNA Gene Therapy Targeting Huntingtin for the Treatment of Huntington's Disease

Pengcheng Zhou,Fen Chen,Xin Wang,Emily Christensen,Jeff Thompson, Mathieu Nonnnenmacher,Maria Scheel,Xiao-Qin Ren,Wei Wang,Xiaochuan Zhou,Lisa Stanek,Bryan Mastis,

MOLECULAR THERAPY（2018）

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