86 related articles for article (PubMed ID: 17460354)
1. Functional polymorphisms of the Lss and Fdft1 genes in laboratory rats.
Mori M; Sawashita J; Higuchi K
Exp Anim; 2007 Apr; 56(2):93-101. PubMed ID: 17460354
[TBL] [Abstract][Full Text] [Related]
2. Lanosterol synthase mutations cause cholesterol deficiency-associated cataracts in the Shumiya cataract rat.
Mori M; Li G; Abe I; Nakayama J; Guo Z; Sawashita J; Ugawa T; Nishizono S; Serikawa T; Higuchi K; Shumiya S
J Clin Invest; 2006 Feb; 116(2):395-404. PubMed ID: 16440058
[TBL] [Abstract][Full Text] [Related]
3. Role of squalene synthase in prostate cancer risk and the biological aggressiveness of human prostate cancer.
Fukuma Y; Matsui H; Koike H; Sekine Y; Shechter I; Ohtake N; Nakata S; Ito K; Suzuki K
Prostate Cancer Prostatic Dis; 2012 Dec; 15(4):339-45. PubMed ID: 22546838
[TBL] [Abstract][Full Text] [Related]
4. Roles of Farnesyl-Diphosphate Farnesyltransferase 1 in Tumour and Tumour Microenvironments.
Ha NT; Lee CH
Cells; 2020 Oct; 9(11):. PubMed ID: 33113804
[TBL] [Abstract][Full Text] [Related]
5. Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex.
Romano MT; Tafazzoli A; Mattern M; Sivalingam S; Wolf S; Rupp A; Thiele H; Altmüller J; Nürnberg P; Ellwanger J; Gambon R; Baumer A; Kohlschmidt N; Metze D; Holdenrieder S; Paus R; Lütjohann D; Frank J; Geyer M; Bertolini M; Kokordelis P; Betz RC
Am J Hum Genet; 2018 Nov; 103(5):777-785. PubMed ID: 30401459
[TBL] [Abstract][Full Text] [Related]
6. Role of FDFT1 polymorphism for fibrosis progression in patients with chronic hepatitis C.
Stättermayer AF; Rutter K; Beinhardt S; Wrba F; Scherzer TM; Strasser M; Hofer H; Steindl-Munda P; Trauner M; Ferenci P
Liver Int; 2014 Mar; 34(3):388-95. PubMed ID: 23870067
[TBL] [Abstract][Full Text] [Related]
7. Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice.
Wada Y; Kikuchi A; Kaga A; Shimizu N; Ito J; Onuma R; Fujishima F; Totsune E; Sato R; Niihori T; Shirota M; Funayama R; Sato K; Nakazawa T; Nakayama K; Aoki Y; Aiba S; Nakagawa K; Kure S
PLoS Genet; 2020 Feb; 16(2):e1008628. PubMed ID: 32101538
[TBL] [Abstract][Full Text] [Related]
8. Characterization of farnesyl diphosphate farnesyl transferase 1 (FDFT1) expression in cancer.
Tüzmen Ş; Hostetter G; Watanabe A; Ekmekçi C; Carrigan PE; Shechter I; Kallioniemi O; Miller LJ; Mousses S
Per Med; 2019 Jan; 16(1):51-65. PubMed ID: 30468409
[TBL] [Abstract][Full Text] [Related]
9. The Polymorphism rs2968 of
Zou X; Wang H; Zhou D; Liu Z; Wang Y; Deng G; Guan H
DNA Cell Biol; 2020 Nov; 39(11):1970-1975. PubMed ID: 32877255
[TBL] [Abstract][Full Text] [Related]
10. Exclusion of CTSB and FDFT1 as positional and functional candidate genes for keratolytic winter erythema (KWE).
Hobbs A; Aron S; Hartshorne S; Hull PR; Ramsay M
J Dermatol Sci; 2012 Jan; 65(1):58-62. PubMed ID: 21945151
[TBL] [Abstract][Full Text] [Related]
11. Functional polymorphisms in inbred rat strains and their allele frequencies in commercially available outbred stocks.
Kuramoto T; Nakanishi S; Serikawa T
Physiol Genomics; 2008 Apr; 33(2):205-11. PubMed ID: 18212005
[TBL] [Abstract][Full Text] [Related]
12. The mechanism and clinical application of farnesyl diphosphate farnesyltransferase 1 in cancer metabolism.
Li N; Wang G; Guo M; Zhu N; Yu W
Biochem Biophys Res Commun; 2024 Jul; 719():150046. PubMed ID: 38749088
[TBL] [Abstract][Full Text] [Related]
13. Mapping of the GATA4, NEIL2, FDFT1 genes and CTSB-associated microsatellites to the centromeric region of BTA8.
Plis-Finarov A; Hudson H; Roe B; Ron M; Seroussi E
Anim Genet; 2004 Apr; 35(2):154-5. PubMed ID: 15025586
[No Abstract] [Full Text] [Related]
14. Potential role of nonstatin cholesterol lowering agents.
Trapani L; Segatto M; Ascenzi P; Pallottini V
IUBMB Life; 2011 Nov; 63(11):964-71. PubMed ID: 21990243
[TBL] [Abstract][Full Text] [Related]
15. Protective mechanism of fdft1 in steroid hormone synthesis pathway in SD rats with acute hypoxic injury.
Lin X; Wang H; Pu X
Genes Genomics; 2020 Nov; 42(11):1319-1326. PubMed ID: 32980992
[TBL] [Abstract][Full Text] [Related]
16. Studies of CTNNBL1 and FDFT1 variants and measures of obesity: analyses of quantitative traits and case-control studies in 18,014 Danes.
Andreasen CH; Mogensen MS; Borch-Johnsen K; Sandbaek A; Lauritzen T; Almind K; Hansen L; Jørgensen T; Pedersen O; Hansen T
BMC Med Genet; 2009 Feb; 10():17. PubMed ID: 19245693
[TBL] [Abstract][Full Text] [Related]
17. K45R variant of squalene synthase increases total cholesterol levels in two study samples from a French Canadian population.
Do R; Paré G; Montpetit A; Hudson TJ; Gaudet D; Engert JC
Hum Mutat; 2008 May; 29(5):689-94. PubMed ID: 18350552
[TBL] [Abstract][Full Text] [Related]
18. Squalene Synthase Deficiency: Clinical, Biochemical, and Molecular Characterization of a Defect in Cholesterol Biosynthesis.
Coman D; Vissers LELM; Riley LG; Kwint MP; Hauck R; Koster J; Geuer S; Hopkins S; Hallinan B; Sweetman L; Engelke UFH; Burrow TA; Cardinal J; McGill J; Inwood A; Gurnsey C; Waterham HR; Christodoulou J; Wevers RA; Pitt J
Am J Hum Genet; 2018 Jul; 103(1):125-130. PubMed ID: 29909962
[TBL] [Abstract][Full Text] [Related]
19. Isolation of a Genomic Region Affecting Most Components of Metabolic Syndrome in a Chromosome-16 Congenic Rat Model.
Šedová L; Pravenec M; Křenová D; Kazdová L; Zídek V; Krupková M; Liška F; Křen V; Šeda O
PLoS One; 2016; 11(3):e0152708. PubMed ID: 27031336
[TBL] [Abstract][Full Text] [Related]
20. [Analyze on the expression differences of key genes in saponins biosynthesize in Eleutherococcus senticosus and its callus].
Xing ZB; Wu P; Long YH; He S; Liang NS
Zhong Yao Cai; 2012 Aug; 35(8):1210-3. PubMed ID: 23320349
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
