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Anil G. Menon
Researcher at University of Cincinnati Academic Health Center
Publications - 95
Citations - 8161
Anil G. Menon is an academic researcher from University of Cincinnati Academic Health Center. The author has contributed to research in topics: Gene & Chromosomal translocation. The author has an hindex of 43, co-authored 95 publications receiving 7820 citations. Previous affiliations of Anil G. Menon include Harvard University & University of Bonn.
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A novel moesin-, ezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressor
James A. Trofatter,Mia MacCollin,Joni L. Rutter,Jill R. Murrell,Mabel P. Duyao,Dilys M. Parry,Roswell Eldridge,Nikolai Kley,Anil G. Menon,K Pulaski,Volker H. Haase,Christine Ambrose,David J. Munroe,Catherine Bove,Jonathan L. Haines,Robert L. Martuza,Marcy E. MacDonald,Bernd R. Seizinger,M. Priscilla Short,Alan Buckler,James F. Gusella +20 more
TL;DR: A candidate gene for the NF2 tumor suppressor that has suffered nonoverlapping deletions in DNA from two independent NF2 families and alterations in meningiomas from two unrelated NF2 patients is identified.
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Genetic and environmental risk factors for intracerebral hemorrhage: preliminary results of a population-based study.
Daniel Woo,Laura Sauerbeck,Brett M. Kissela,Jane Khoury,Jerzy P. Szaflarski,James Gebel,Rakesh Shukla,Arthur M. Pancioli,Edward C. Jauch,Anil G. Menon,Ranjan Deka,Janice Carrozzella,Charles J Moomaw,Robert N. Fontaine,Joseph P. Broderick +14 more
TL;DR: In this paper, the authors report a preplanned, midpoint analysis of the first population-based, case-control study that examines both genetic and environmental risk factors of ICH.
Journal ArticleDOI
Chromosome 17p deletions and p53 gene mutations associated with the formation of malignant neurofibrosarcomas in von Recklinghausen neurofibromatosis.
Anil G. Menon,Kevin M. Anderson,V M Riccardi,Richard Y. Chung,Jean M. Whaley,David W. Yandell,G. E. Farmer,Richard N. Freiman,Jeng-Shin Lee,Fugen Li +9 more
TL;DR: The formation of malignant neurofibrosarcomas may result from several independent genetic events including mutation of the NF1 gene, whose mechanism of tumorigenesis remains uncertain, and subsequent loss of a "tumor suppressor" gene on 17p, most likely p53.
Journal Article
Mutations of the PATCHED Gene in Several Types of Sporadic Extracutaneous Tumors
Jingwu Xie,Ronald L. Johnson,Xiaoli Zhang,John W. Bare,Fred Waldman,Philip H. Cogen,Anil G. Menon,Robert S. Warren,Ling Chun Chen,Matthew P. Scott,Ervin H. Epstein +10 more
TL;DR: It is found that 2 of 14 sporadic medulloblastomas bear somatic nonsense mutations in one copy of the gene and also deletion of the other copy, and that missense mutations in PTCH are identified in two of seven breast carcinomas, one of nine meningiomas, and one colon cancer cell line.
Journal ArticleDOI
Salivary acinar cells from aquaporin 5-deficient mice have decreased membrane water permeability and altered cell volume regulation.
Carissa M. Krane,James E. Melvin,Ha Van Nguyen,Linda Richardson,Jennifer E. Towne,Thomas Doetschman,Anil G. Menon +6 more
TL;DR: In this paper, the authors show that the decreased salivary flow rate and increased tonicity of the saliva secreted by Aqp5 −/− mice in response to pilocarpine stimulation are not caused by changes in whole body fluid homeostasis, indicated by similar blood gas and electrolyte concentrations in urine and blood in wild-type and AQP5− mice.