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Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1928 1
1947 1
1953 1
1954 1
1958 1
1960 2
1961 6
1962 3
1964 1
1967 1
1968 3
1969 3
1970 3
1971 4
1972 4
1973 3
1974 1
1975 2
1976 3
1977 3
1978 3
1979 7
1980 1
1981 1
1982 5
1984 2
1986 6
1987 6
1988 10
1989 8
1990 8
1991 9
1992 8
1993 7
1994 12
1995 14
1996 12
1997 17
1998 15
1999 9
2000 10
2001 16
2002 18
2003 15
2004 9
2005 8
2006 10
2007 12
2008 6
2009 7
2010 5
2011 6
2012 4
2013 4
2014 3
2015 3
2016 3
2017 1
2018 2
2020 2
2024 0

Text availability

Article attribute

Article type

Publication date

PubMed (OMIM) for id: 7428

342 results

Results by year

Filters applied: . Clear all
Page 1
Genetic predisposition to neural crest-derived tumors: revisiting the role of KIF1B.
Cardot Bauters C, Leteurtre E, Carnaille B, Do Cao C, Espiard S, Penven M, Destailleur E, Szuster I, Lovecchio T, Leclerc J, Frénois F, Esquivel E, Dahia PLM, Ait-Yahya E, Crépin M, Pigny P. Cardot Bauters C, et al. Endocr Connect. 2020 Oct;9(10):1042-1050. doi: 10.1530/EC-20-0460. Endocr Connect. 2020. PMID: 33112832 Free PMC article.
Effects of Germline VHL Deficiency on Growth, Metabolism, and Mitochondria.
Perrotta S, Roberti D, Bencivenga D, Corsetto P, O'Brien KA, Caiazza M, Stampone E, Allison L, Fleck RA, Scianguetta S, Tartaglione I, Robbins PA, Casale M, West JA, Franzini-Armstrong C, Griffin JL, Rizzo AM, Sinisi AA, Murray AJ, Borriello A, Formenti F, Della Ragione F. Perrotta S, et al. N Engl J Med. 2020 Feb 27;382(9):835-844. doi: 10.1056/NEJMoa1907362. N Engl J Med. 2020. PMID: 32101665
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. Lenglet M, et al. Blood. 2018 Aug 2;132(5):469-483. doi: 10.1182/blood-2018-03-838235. Epub 2018 Jun 11. Blood. 2018. PMID: 29891534 Free article.
Daam2 driven degradation of VHL promotes gliomagenesis.
Zhu W, Krishna S, Garcia C, Lin CJ, Mitchell BD, Scott KL, Mohila CA, Creighton CJ, Yoo SH, Lee HK, Deneen B. Zhu W, et al. Elife. 2017 Oct 20;6:e31926. doi: 10.7554/eLife.31926. Elife. 2017. PMID: 29053101 Free PMC article.
pVHL suppresses kinase activity of Akt in a proline-hydroxylation-dependent manner.
Guo J, Chakraborty AA, Liu P, Gan W, Zheng X, Inuzuka H, Wang B, Zhang J, Zhang L, Yuan M, Novak J, Cheng JQ, Toker A, Signoretti S, Zhang Q, Asara JM, Kaelin WG Jr, Wei W. Guo J, et al. Science. 2016 Aug 26;353(6302):929-32. doi: 10.1126/science.aad5755. Science. 2016. PMID: 27563096 Free PMC article.
A germline mutation in PBRM1 predisposes to renal cell carcinoma.
Benusiglio PR, Couvé S, Gilbert-Dussardier B, Deveaux S, Le Jeune H, Da Costa M, Fromont G, Memeteau F, Yacoub M, Coupier I, Leroux D, Méjean A, Escudier B, Giraud S, Gimenez-Roqueplo AP, Blondel C, Frouin E, Teh BT, Ferlicot S, Bressac-de Paillerets B, Richard S, Gad S. Benusiglio PR, et al. J Med Genet. 2015 Jun;52(6):426-30. doi: 10.1136/jmedgenet-2014-102912. Epub 2015 Apr 24. J Med Genet. 2015. PMID: 25911086
342 results