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326 related items for PubMed ID: 20197624
21. Increased size of solid organs in patients with Chuvash polycythemia and in mice with altered expression of HIF-1alpha and HIF-2alpha. Yoon D, Okhotin DV, Kim B, Okhotina Y, Okhotin DJ, Miasnikova GY, Sergueeva AI, Polyakova LA, Maslow A, Lee Y, Semenza GL, Prchal JT, Gordeuk VR. J Mol Med (Berl); 2010 May; 88(5):523-30. PubMed ID: 20140661 [Abstract] [Full Text] [Related]
23. Identification of a new VHL exon and complex splicing alterations in familial erythrocytosis or von Hippel-Lindau disease. Lenglet M, Robriquet F, Schwarz K, Camps C, Couturier A, Hoogewijs D, Buffet A, Knight SJL, Gad S, Couvé S, Chesnel F, Pacault M, Lindenbaum P, Job S, Dumont S, Besnard T, Cornec M, Dreau H, Pentony M, Kvikstad E, Deveaux S, Burnichon N, Ferlicot S, Vilaine M, Mazzella JM, Airaud F, Garrec C, Heidet L, Irtan S, Mantadakis E, Bouchireb K, Debatin KM, Redon R, Bezieau S, Bressac-de Paillerets B, Teh BT, Girodon F, Randi ML, Putti MC, Bours V, Van Wijk R, Göthert JR, Kattamis A, Janin N, Bento C, Taylor JC, Arlot-Bonnemains Y, Richard S, Gimenez-Roqueplo AP, Cario H, Gardie B. Blood; 2018 Aug 02; 132(5):469-483. PubMed ID: 29891534 [Abstract] [Full Text] [Related]
29. Suppression of von Hippel-Lindau Protein in Fibroblasts Protects against Bleomycin-Induced Pulmonary Fibrosis. Zhou Q, Chen T, Zhang W, Bozkanat M, Li Y, Xiao L, van Breemen RB, Christman JW, Sznajder JI, Zhou G. Am J Respir Cell Mol Biol; 2016 May 02; 54(5):728-39. PubMed ID: 26488390 [Abstract] [Full Text] [Related]
30. HIF-2α-pVHL complex reveals broad genotype-phenotype correlations in HIF-2α-driven disease. Tarade D, Robinson CM, Lee JE, Ohh M. Nat Commun; 2018 Aug 22; 9(1):3359. PubMed ID: 30135421 [Abstract] [Full Text] [Related]
32. Increased transferrin protects from thrombosis in Chuvash erythrocytosis. Shah BN, Zhang X, Sergueeva AI, Miasnikova GY, Ganz T, Prchal JT, Gordeuk VR. Am J Hematol; 2023 Oct 22; 98(10):1532-1539. PubMed ID: 37435906 [Abstract] [Full Text] [Related]
33. Genotype-phenotype analysis of von Hippel-Lindau syndrome in Korean families: HIF-α binding site missense mutations elevate age-specific risk for CNS hemangioblastoma. Lee JS, Lee JH, Lee KE, Kim JH, Hong JM, Ra EK, Seo SH, Lee SJ, Kim MJ, Park SS, Seong MW. BMC Med Genet; 2016 Jul 20; 17(1):48. PubMed ID: 27439424 [Abstract] [Full Text] [Related]
36. VHL gene methylation contributes to excessive erythrocytosis in chronic mountain sickness rat model by upregulating the HIF-2α/EPO pathway. Yang M, Zhu M, Song K, Wuren T, Yan J, Ge RL, Ji L, Cui S. Life Sci; 2021 Feb 01; 266():118873. PubMed ID: 33309718 [Abstract] [Full Text] [Related]
38. Pancreatic endocrine microadenomatosis in patients with von Hippel-Lindau disease: characterization by VHL/HIF pathway proteins expression. Périgny M, Hammel P, Corcos O, Larochelle O, Giraud S, Richard S, Sauvanet A, Belghiti J, Ruszniewski P, Bedossa P, Couvelard A. Am J Surg Pathol; 2009 May 01; 33(5):739-48. PubMed ID: 19238077 [Abstract] [Full Text] [Related]