Disruption of the HIF-1 pathway in individuals with Ollier disease and Maffucci syndrome.
Saved in:
| Title: | Disruption of the HIF-1 pathway in individuals with Ollier disease and Maffucci syndrome. |
|---|---|
| Authors: | Poll SR; McKusick-Nathans Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America., Martin R; McKusick-Nathans Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America., Wohler E; McKusick-Nathans Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America., Partan ES; McKusick-Nathans Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America., Walek E; McKusick-Nathans Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America., Salman S; McKusick-Nathans Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America., Groepper D; Department of Pediatrics, Southern Illinois University School of Medicine, Springfield, Illinois, United States of America., Kratz L; McKusick-Nathans Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America., Cernach M; Universidade Metropolitana de Santos, Santos, São Paulo, Brazil., Jesus-Garcia R; Department of Orthopedics-Oncology, Universidade Federal de São Paulo, São Paulo, Brazil., Haldeman-Englert C; Mission Fullerton Genetics Center, Asheville, North Carolina, United States of America., Choi YJ; Department of Neurology, University of California, Irvine, California, United States of America., Morris CD; Department of Orthopedic Surgery, Johns Hopkins School of Medicine, Baltimore, Maryland, United States of America.; Department of Oncology, Johns Hopkins School of Medicine, Baltimore, Maryland, United States of America., Cohen B; Department of Dermatology, Johns Hopkins School of Medicine, Baltimore, Maryland, Untied States of America., Hoover-Fong J; McKusick-Nathans Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America., Valle D; McKusick-Nathans Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America., Semenza GL; McKusick-Nathans Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America., Sobreira NLM; McKusick-Nathans Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America. |
| Source: | PLoS genetics [PLoS Genet] 2022 Dec 08; Vol. 18 (12), pp. e1010504. Date of Electronic Publication: 2022 Dec 08 (Print Publication: 2022). |
| Publication Type: | Journal Article; Research Support, N.I.H., Extramural |
| Journal Info: | Publisher: Public Library of Science Country of Publication: United States NLM ID: 101239074 Publication Model: eCollection Cited Medium: Internet ISSN: 1553-7404 (Electronic) Linking ISSN: 15537390 NLM ISO Abbreviation: PLoS Genet Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
|
Full text is not displayed to guests.
Login for full access.
|
|
| ISSN: | 1553-7404 |
|---|---|
| DOI: | 10.1371/journal.pgen.1010504 |