Extracellular Hsp90 mediates an NF-κB dependent inflammatory stromal program: Implications for the prostate tumor microenvironment.

Autor: Bohonowych, JE, Hance, MW, Nolan, KD, Defee, M, Parsons, CH, Isaacs, JS

Publikováno v: Prostate; Feb2014, Vol. 74 Issue 4, p395-407, 13p

Comparative analysis of novel and conventional Hsp90 inhibitors on HIF activity and angiogenic potential in clear cell renal cell carcinoma: implications for clinical evaluation

Autor: Bohonowych Jessica ES, Peng Shuping, Gopal Udhayakumar, Hance Michael W, Wing Shane B, Argraves Kelley M, Lundgren Karen, Isaacs Jennifer S

Publikováno v: BMC Cancer, Vol 11, Iss 1, p 520 (2011)

Abstract Background Perturbing Hsp90 chaperone function targets hypoxia inducible factor (HIF) function in a von Hippel-Lindau (VHL) independent manner, and represents an approach to combat the contribution of HIF to cell renal carcinoma (CCRCC) prog

Externí odkaz: https://doaj.org/article/4b2af3da60ea4b0a9236ca75acc539e8

Feeding tube use and complications in Prader-Willi syndrome: Data from the Global Prader-Willi Syndrome Registry.

Autor: Roy SM; Cook Children's Medical Center, Fort Worth, Texas, USA., Rafferty D; Cook Children's Medical Center, Fort Worth, Texas, USA., Trejo A; Cook Children's Medical Center, Fort Worth, Texas, USA., Hamilton L; Cook Children's Medical Center, Fort Worth, Texas, USA., Bohonowych JE; Foundation for Prader-Willi Research, California, USA., Strong TV; Foundation for Prader-Willi Research, California, USA., Ambartsumyan L; Seattle Children's Hospital, Washington, USA., Cantu S; Cook Children's Medical Center, Fort Worth, Texas, USA., Scheimann A; The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.; Texas Children's Hospital, Houston, Texas, USA., Duis J; Children's Hospital Colorado, Aurora, Colorado, USA.; SequenceMD, Denver, Colorado, USA.

Publikováno v: American journal of medical genetics. Part A [Am J Med Genet A] 2024 Jun; Vol. 194 (6), pp. e63546. Date of Electronic Publication: 2024 Feb 01.

Age of diagnosis for children with chromosome 15q syndromes.

Autor: Wheeler AC; Genomics, Ethics, and Translational Research Program, RTI International, 3040 W. Cornwallis Rd, Research Triangle Park, NC, 27709, USA. acwheeler@rti.org., Gantz MG; Genomics, Ethics, and Translational Research Program, RTI International, 3040 W. Cornwallis Rd, Research Triangle Park, NC, 27709, USA., Cope H; Genomics, Ethics, and Translational Research Program, RTI International, 3040 W. Cornwallis Rd, Research Triangle Park, NC, 27709, USA., Strong TV; Foundation for Prader Willi Research, Covina, CA, USA., Bohonowych JE; Foundation for Prader Willi Research, Covina, CA, USA., Moore A; Angelman Syndrome Foundation, Aurora, IL, USA., Vogel-Farley V; Dup15q Alliance, Matthews, NC, USA.

Publikováno v: Journal of neurodevelopmental disorders [J Neurodev Disord] 2023 Nov 07; Vol. 15 (1), pp. 37. Date of Electronic Publication: 2023 Nov 07.

Incidence of strabismus, strabismus surgeries, and other vision conditions in Prader-Willi syndrome: data from the Global Prader-Willi Syndrome Registry.

Autor: Bohonowych JE; Foundation for Prader-Willi Research, Walnut, CA, USA., Vrana-Diaz CJ; Foundation for Prader-Willi Research, Walnut, CA, USA., Miller JL; University of Florida, Gainesville, FL, USA., McCandless SE; University of Colorado Anschutz Medical Campus, Aurora, CO, USA., Strong TV; Foundation for Prader-Willi Research, Walnut, CA, USA. theresa.strong@fpwr.org.

Publikováno v: BMC ophthalmology [BMC Ophthalmol] 2021 Aug 12; Vol. 21 (1), pp. 296. Date of Electronic Publication: 2021 Aug 12.