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A. Julian Garvin
Researcher at Wake Forest University
Publications - 14
Citations - 1185
A. Julian Garvin is an academic researcher from Wake Forest University. The author has contributed to research in topics: Wilms' tumor & Sarcoma. The author has an hindex of 11, co-authored 14 publications receiving 1107 citations. Previous affiliations of A. Julian Garvin include Johns Hopkins University School of Medicine.
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Journal ArticleDOI
Primary Renal Neoplasms with the ASPL-TFE3 Gene Fusion of Alveolar Soft Part Sarcoma: A Distinctive Tumor Entity Previously Included among Renal Cell Carcinomas of Children and Adolescents
Pedram Argani,Cristina R. Antonescu,Peter B. Illei,Man Yee Lui,Charles F. Timmons,T. Robert Newbury,Victor E. Reuter,A. Julian Garvin,Antonio R. Perez-Atayde,Jonathan A. Fletcher,J. Bruce Beckwith,Julia A. Bridge,Marc Ladanyi +12 more
TL;DR: A subset of tumors previously considered to be RCC in young people are in fact genetically related to ASPS, although their distinctive morphological and genetic features justify their classification as a distinctive neoplastic entity.
Journal ArticleDOI
Characterization of the chromosomal translocation t(10;17)(q22;p13) in clear cell sarcoma of kidney
Elaine O'Meara,Deirdre Stack,Cheng-Han Lee,A. Julian Garvin,Thomas Morris,Pedram Argani,Jeong S. Han,Jenny Karlsson,David Gisselson,Ivo Leuschner,Manfred Gessler,Norbert Graf,Jonathan A. Fletcher,Maureen J. O'Sullivan,Maureen J. O'Sullivan +14 more
TL;DR: Elucidation of the role of YWHAE‐FAM22 in CCSK will assist development of more efficient and targeted therapies for this childhood cancer, which currently has poor outcomes.
Journal ArticleDOI
Advances in Cytochemical Methods for Detection of Apoptosis
TL;DR: The utility of a prototype of new assays for caspase substrate cleavage products, the detection of cleaved cytokeratin 18, holds the greatest promise for specific detection of apoptosis in cells either in cell culture or in intact tissues.
Journal ArticleDOI
Novel FOXF1 mutations in sporadic and familial cases of alveolar capillary dysplasia with misaligned pulmonary veins imply a role for its DNA binding domain
Partha Sen,Yaping Yang,Colby Navarro,Iris Silva,Przemyslaw Szafranski,Katarzyna E. Kolodziejska,Avinash V. Dharmadhikari,Hasnaa Mostafa,Harry P.W. Kozakewich,Debra L. Kearney,John B. Cahill,Merrissa Whitt,Masha Bilic,Linda R. Margraf,Adrian Charles,Jack Goldblatt,Kathleen Gibson,Patrick E. Lantz,A. Julian Garvin,John K. Petty,Zeina N. Kiblawi,Craig W. Zuppan,Allyn McConkie-Rosell,Marie T. McDonald,Stacey L. Peterson-Carmichael,Jane T. Gaede,Binoy Shivanna,Deborah Schady,Philippe Friedlich,Stephen R. Hays,Irene Valenzuela Palafoll,Ulrike Siebers-Renelt,Axel Bohring,Laura S. Finn,Joseph R. Siebert,Csaba Galambos,Lananh Nguyen,Melissa M. Riley,Nicolas Chassaing,Adeline Vigouroux,Gustavo Rocha,Susana Fernandes,Jane E. Brumbaugh,Kari D Roberts,Luk Ho-ming,Ivan F M Lo,Stephen Lam,Romana Gerychová,Marta Jezova,Iveta Valášková,Florence Fellmann,Katayoun Afshar,Eric Giannoni,Vincent Muhlethaler,Jinlong Liang,Jacques S. Beckmann,Janet Lioy,Hitesh Deshmukh,Lakshmi Srinivasan,Daniel T. Swarr,Melissa Sloman,Charles Shaw-Smith,Rosa L. E. van Loon,Cecilia Hagman,Yves Sznajer,Catherine Barrea,Christine Galant,Thierry Detaille,Jennifer A. Wambach,F. Sessions Cole,Aaron Hamvas,Lawrence S. Prince,Karin E. M. Diderich,Alice S. Brooks,Robert M. Verdijk,Hari Ravindranathan,Ella Sugo,David Mowat,Michael L. Baker,Claire Langston,Stephen E. Welty,Pawel Stankiewicz +81 more
TL;DR: The results corroborate and extend the previous observations and further establish involvement of FOXF1 in ACD/MPV and lung organogenesis.
Journal Article
Gene Expression Profiling of Favorable Histology Wilms Tumors and Its Correlation with Clinical Features
Masayuki Takahashi,Ximing J. Yang,Todd T. Lavery,Kyle A. Furge,Bart O. Williams,Maria Tretiakova,Anthony G. Montag,Nicholas J. Vogelzang,Gian G. Re,A. Julian Garvin,Stefan Söderhäll,Susumu Kagawa,Debra Hazel-Martin,Agneta Nordenskjöld,Bin Tean Teh +14 more
TL;DR: The data suggest that high expression of topoisomerase IIalpha and microtubule-related genes such as tubulin and stathmin 1 may be related to the high chemosensitivity of WT and lead to the discovery of new drugs for WT.