98 related articles for article (PubMed ID: 12696072)
21. Mutations in the SDHB gene are associated with extra-adrenal and/or malignant phaeochromocytomas.
Gimenez-Roqueplo AP; Favier J; Rustin P; Rieubland C; Crespin M; Nau V; Khau Van Kien P; Corvol P; Plouin PF; Jeunemaitre X;
Cancer Res; 2003 Sep; 63(17):5615-21. PubMed ID: 14500403
[TBL] [Abstract][Full Text] [Related]
22. A novel mannose-binding lectin-associated serine protease 1/3 gene variant.
Weiss G; Madsen HO; Garred P
Scand J Immunol; 2007 May; 65(5):430-4. PubMed ID: 17444953
[TBL] [Abstract][Full Text] [Related]
23. A novel polymorphism in exon 10 of the factor V gene inducing an amino acid replacement of arginine to lysine at codon 485.
Ozawa T; Niiya K; Ejiri N; Sakuragawa N
Thromb Haemost; 1997 Nov; 78(5):1419-20. PubMed ID: 9408032
[No Abstract] [Full Text] [Related]
24. Identification of 6 new polymorphisms, g.11177G>A, g.14622C>T (R49C), g.17540T>C, g.17639T>C, g.30929T>C, g.31074G>A (R454Q), in the human microsomal epoxide hydrolase gene (EPHX1) in a French population.
Belmahdi F; Chevalier D; Lo-Guidice JM; Allorge D; Cauffiez C; Lafitte JJ; Broly F
Hum Mutat; 2000 Nov; 16(5):450. PubMed ID: 11058921
[No Abstract] [Full Text] [Related]
25. Hypertrophic cardiomyopathy with mitochondrial myopathy. A new phenotype of complex II defect.
Angelini C; Melacini P; Valente ML; Reichmann H; Carrozzo R; Fanin M; Vergani L; Boffa GM; Martinuzzi A; Fasoli G
Jpn Heart J; 1993 Jan; 34(1):63-77. PubMed ID: 8515573
[TBL] [Abstract][Full Text] [Related]
26. Identification of a polymorphism (G83S) in the TWIST gene in Taiwanese.
Yang CF; Wu JY; Tsai FJ; Lee CC; Lin WD
Hum Mutat; 2000 Nov; 16(5):448. PubMed ID: 11058914
[No Abstract] [Full Text] [Related]
27. A polymorphism of the beta1-adrenergic receptor is associated with low extraversion.
Stein MB; Schork NJ; Gelernter J
Biol Psychiatry; 2004 Aug; 56(4):217-24. PubMed ID: 15312808
[TBL] [Abstract][Full Text] [Related]
28. Common polymorphism in p53 intron 2, IVS2+38G>C.
Verselis SJ; Li FP
Hum Mutat; 2000 Aug; 16(2):181. PubMed ID: 10923052
[No Abstract] [Full Text] [Related]
29. Further evidence supporting the association between the dopamine receptor D2 Ser/Cys311 variant and disorganized symptomatology of schizophrenia.
Serretti A; Lilli R; Lorenzi C; Smeraldi E
Schizophr Res; 2000 Jun; 43(2-3):161-2. PubMed ID: 11001590
[No Abstract] [Full Text] [Related]
30. Two new mutations (H106P and L178V) in the protoporphyrinogen oxidase gene in Argentinean patients with variegate porphyria.
De Siervi A; Parera VE; del C Batlle AM; Rossetti MV
Hum Mutat; 2000 Dec; 16(6):532. PubMed ID: 11102990
[No Abstract] [Full Text] [Related]
31. Identification of single-nucleotide polymorphisms of the human neurokinin 1 receptor gene and pharmacological characterization of a Y192H variant.
Randolph GP; Simon JS; Arreaza MG; Qiu P; Lachowicz JE; Duffy RA
Pharmacogenomics J; 2004; 4(6):394-402. PubMed ID: 15452552
[TBL] [Abstract][Full Text] [Related]
32. SDHB, SDHC, and SDHD mutation screen in sporadic and familial head and neck paragangliomas.
Mhatre AN; Li Y; Feng L; Gasperin A; Lalwani AK
Clin Genet; 2004 Nov; 66(5):461-6. PubMed ID: 15479192
[TBL] [Abstract][Full Text] [Related]
33. Single nucleotide polymorphisms in succinate dehydrogenase subunits and citrate synthase genes: association results for impaired spermatogenesis.
Bonache S; Martínez J; Fernández M; Bassas L; Larriba S
Int J Androl; 2007 Jun; 30(3):144-52. PubMed ID: 17298551
[TBL] [Abstract][Full Text] [Related]
34. [Mitochondrial cytopathies: identification of responsible nuclear genes].
Paquis V
Arch Pediatr; 1996 Sep; 3(9):915-6. PubMed ID: 8949357
[No Abstract] [Full Text] [Related]
35. Cloning, mapping and association study with carcass traits of the porcine SDHD gene.
Zhu ZM; Zhang JB; Li K; Zhao SH
Anim Genet; 2005 Jun; 36(3):191-5. PubMed ID: 15932396
[TBL] [Abstract][Full Text] [Related]
36. SDH mutations in patients affected by paraganglioma syndromes: a personal experience.
Mannelli M; Simi L; Ercolino T; Gaglianò MS; Becherini L; Vinci S; Sestini R; Gensini F; Pinzani P; Mascalchi M; Guerrini L; Pratesi C; Nesi G; Torti F; Cipollini F; Bernini GP; Genuardi M
Ann N Y Acad Sci; 2006 Aug; 1073():183-9. PubMed ID: 17102085
[TBL] [Abstract][Full Text] [Related]
37. SDHD mutations in head and neck paragangliomas result in destabilization of complex II in the mitochondrial respiratory chain with loss of enzymatic activity and abnormal mitochondrial morphology.
Douwes Dekker PB; Hogendoorn PC; Kuipers-Dijkshoorn N; Prins FA; van Duinen SG; Taschner PE; van der Mey AG; Cornelisse CJ
J Pathol; 2003 Nov; 201(3):480-6. PubMed ID: 14595761
[TBL] [Abstract][Full Text] [Related]
38. TLR2 Arg753Gly, TLR4 Asp299Gly and Thr399Ile gene polymorphisms are not associated with chronic periodontitis in a Turkish population.
Berdeli A; Emingil G; Han Saygan B; Gürkan A; Atilla G; Köse T; Baylas H
J Clin Periodontol; 2007 Jul; 34(7):551-7. PubMed ID: 17555409
[TBL] [Abstract][Full Text] [Related]
39. Functional characterization of a nucleoside-derived drug transporter variant (hCNT3C602R) showing altered sodium-binding capacity.
Errasti-Murugarren E; Cano-Soldado P; Pastor-Anglada M; Casado FJ
Mol Pharmacol; 2008 Feb; 73(2):379-86. PubMed ID: 17993510
[TBL] [Abstract][Full Text] [Related]
40. Chromosome 11 monosomy in conjunction with a mutated SDHD initiation codon in nonfamilial paraganglioma cases.
Riemann K; Sotlar K; Kupka S; Braun S; Zenner HP; Preyer S; Pfister M; Pusch CM; Blin N
Cancer Genet Cytogenet; 2004 Apr; 150(2):128-35. PubMed ID: 15066320
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
