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Molecular and Cellular Biology|September 7, 2002
Control of the hypoxic response in Drosophila melanogaster by the basic helix-loop-helix PAS protein similarSofía Lavista-Llanos, Lázaro Centanin, Maximiliano Irisarri, et al.The Journal of Biological Chemistry|August 23, 2015
Striking Oxygen Sensitivity of the Peptidylglycine α-Amidating Monooxygenase (PAM) in Neuroendocrine CellsPeter D Simpson, Betty A Eipper, Maximiliano J Katz, et al.Cardiovascular Research|March 30, 2002
Genotype at a promoter polymorphism of the interleukin-6 gene is associated with baseline levels of plasma C-reactive proteinMark A Vickers, Fiona R Green, Catherine Terry, et al.Human Molecular Genetics|October 22, 2009
PHF8, a gene associated with cleft lip/palate and mental retardation, encodes for an Nepsilon-dimethyl lysine demethylaseChristoph Loenarz, Wei Ge, Mathew L Coleman, et al.Nature Genetics|March 13, 2012
Common genetic variants at the 11q13.3 renal cancer susceptibility locus influence binding of HIF to an enhancer of cyclin D1 expressionJohannes Schödel, Chiara Bardella, Lina K Sciesielski, et al.Science (New York, N.Y.)|July 6, 2019
Conserved N-terminal cysteine dioxygenases transduce responses to hypoxia in animals and plantsNorma Masson, Thomas P Keeley, Beatrice Giuntoli, et al.JAMA|October 8, 2009
Effects of iron supplementation and depletion on hypoxic pulmonary hypertension: two randomized controlled trialsThomas G Smith, Nick P Talbot, Catherine Privat, et al.Journal of the American Society of Nephrology : JASN|June 29, 2002
Expression of hypoxia-inducible factor-1alpha and -2alpha in hypoxic and ischemic rat kidneysChristian Rosenberger, Stefano Mandriota, Jan Steffen Jürgensen, et al.Proceedings of the National Academy of Sciences of the United States of America|August 5, 2022
Widespread hydroxylation of unstructured lysine-rich protein domains by JMJD6Matthew E Cockman, Yoichiro Sugimoto, Hamish B Pegg, et al.Haematologica|September 22, 2016
Gene panel sequencing improves the diagnostic work-up of patients with idiopathic erythrocytosis and identifies new mutationsCarme Camps, Nayia Petousi, Celeste Bento, et al.Pageof 19