391 related articles for article (PubMed ID: 15579186)
1. Genomic structure of the human gene for protein kinase A regulatory subunit R1-beta (PRKAR1B) on 7p22: no evidence for mutations in familial hyperaldosteronism type II in a large affected kindred.
Elphinstone MS; Gordon RD; So A; Jeske YW; Stratakis CA; Stowasser M
Clin Endocrinol (Oxf); 2004 Dec; 61(6):716-23. PubMed ID: 15579186
[TBL] [Abstract][Full Text] [Related]
2. Further evidence for linkage of familial hyperaldosteronism type II at chromosome 7p22 in Italian as well as Australian and South American families.
Sukor N; Mulatero P; Gordon RD; So A; Duffy D; Bertello C; Kelemen L; Jeske Y; Veglio F; Stowasser M
J Hypertens; 2008 Aug; 26(8):1577-82. PubMed ID: 18622235
[TBL] [Abstract][Full Text] [Related]
3. The human Nramp2 gene: characterization of the gene structure, alternative splicing, promoter region and polymorphisms.
Lee PL; Gelbart T; West C; Halloran C; Beutler E
Blood Cells Mol Dis; 1998 Jun; 24(2):199-215. PubMed ID: 9642100
[TBL] [Abstract][Full Text] [Related]
4. Familial hyperaldosteronism type II is linked to the chromosome 7p22 region but also shows predicted heterogeneity.
So A; Duffy DL; Gordon RD; Jeske YW; Lin-Su K; New MI; Stowasser M
J Hypertens; 2005 Aug; 23(8):1477-84. PubMed ID: 16003173
[TBL] [Abstract][Full Text] [Related]
5. Further study of chromosome 7p22 to identify the molecular basis of familial hyperaldosteronism type II.
Carss KJ; Stowasser M; Gordon RD; O'Shaughnessy KM
J Hum Hypertens; 2011 Sep; 25(9):560-4. PubMed ID: 20927129
[TBL] [Abstract][Full Text] [Related]
6. Mutation analysis of CYP11B1 and CYP11B2 in patients with increased 18-hydroxycortisol production.
Nicod J; Dick B; Frey FJ; Ferrari P
Mol Cell Endocrinol; 2004 Feb; 214(1-2):167-74. PubMed ID: 15062555
[TBL] [Abstract][Full Text] [Related]
7. Examination of chromosome 7p22 candidate genes RBaK, PMS2 and GNA12 in familial hyperaldosteronism type II.
Jeske YW; So A; Kelemen L; Sukor N; Willys C; Bulmer B; Gordon RD; Duffy D; Stowasser M
Clin Exp Pharmacol Physiol; 2008 Apr; 35(4):380-5. PubMed ID: 18307725
[TBL] [Abstract][Full Text] [Related]
8. Alport syndrome. Molecular genetic aspects.
Hertz JM
Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
[TBL] [Abstract][Full Text] [Related]
9. Genomic structure of the human mitochondrial chaperonin genes: HSP60 and HSP10 are localised head to head on chromosome 2 separated by a bidirectional promoter.
Hansen JJ; Bross P; Westergaard M; Nielsen MN; Eiberg H; Børglum AD; Mogensen J; Kristiansen K; Bolund L; Gregersen N
Hum Genet; 2003 Jan; 112(1):71-7. PubMed ID: 12483302
[TBL] [Abstract][Full Text] [Related]
10. Human calcium/calmodulin-dependent protein kinase II gamma gene (CAMK2G): cloning, genomic structure and detection of variants in subjects with type II diabetes.
Gloyn AL; Desai M; Clark A; Levy JC; Holman RR; Frayling TM; Hattersley AT; Ashcroft SJ
Diabetologia; 2002 Apr; 45(4):580-3. PubMed ID: 12032636
[TBL] [Abstract][Full Text] [Related]
11. Exon/intron boundaries, novel polymorphisms, and association analysis with schizophrenia of the human synaptic vesicle monoamine transporter (SVMT) gene.
Kunugi H; Ishida S; Akahane A; Nanko S
Mol Psychiatry; 2001 Jul; 6(4):456-60. PubMed ID: 11443533
[TBL] [Abstract][Full Text] [Related]
12. Mutation analysis and characterization of ATR sequence variants in breast cancer cases from high-risk French Canadian breast/ovarian cancer families.
Durocher F; Labrie Y; Soucy P; Sinilnikova O; Labuda D; Bessette P; Chiquette J; Laframboise R; Lépine J; Lespérance B; Ouellette G; Pichette R; Plante M; Tavtigian SV; Simard J
BMC Cancer; 2006 Sep; 6():230. PubMed ID: 17010193
[TBL] [Abstract][Full Text] [Related]
13. Intronic mutations outside of Alu-repeat-rich domains of the LDL receptor gene are a cause of familial hypercholesterolemia.
Amsellem S; Briffaut D; Carrié A; Rabès JP; Girardet JP; Fredenrich A; Moulin P; Krempf M; Reznik Y; Vialettes B; de Gennes JL; Brukert E; Benlian P
Hum Genet; 2002 Dec; 111(6):501-10. PubMed ID: 12436241
[TBL] [Abstract][Full Text] [Related]
14. 5'-UTR structural organization, transcript expression, and mutational analysis of the human Rab geranylgeranyl transferase alpha-subunit (RABGGTA) gene.
Li W; Detter JC; Weiss HJ; Cramer EM; Zhang Q; Novak EK; Favier R; Kingsmore SF; Swank RT
Mol Genet Metab; 2000 Dec; 71(4):599-608. PubMed ID: 11136552
[TBL] [Abstract][Full Text] [Related]
15. The angiotensin II receptor (Agtr1a): functional regulatory polymorphisms in a locus genetically linked to blood pressure variation in the mouse.
Wong C; Mahapatra NR; Chitbangonsyn S; Mahboubi P; Mahata M; Mahata SK; O'Connor DT
Physiol Genomics; 2003 Jun; 14(1):83-93. PubMed ID: 12697907
[TBL] [Abstract][Full Text] [Related]
16. Organization and alternative splicing of the Caenorhabditis elegans cAMP-dependent protein kinase catalytic-subunit gene (kin-1).
Tabish M; Clegg RA; Rees HH; Fisher MJ
Biochem J; 1999 Apr; 339 ( Pt 1)(Pt 1):209-16. PubMed ID: 10085246
[TBL] [Abstract][Full Text] [Related]
17. Genomic organization and chromosomal assignment of the human voltage-gated Na+ channel beta 1 subunit gene (SCN1B).
Makita N; Sloan-Brown K; Weghuis DO; Ropers HH; George AL
Genomics; 1994 Oct; 23(3):628-34. PubMed ID: 7851891
[TBL] [Abstract][Full Text] [Related]
18. [Identification of a novel splice mutation of low density lipoprotein receptor gene in a Chinese family with familial hypercholesterolemia].
Lin J; Wang LY; Liu S; Pan XD; Du LP; Shi FR; Qin YW; Zhao Q; Guo HY
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Feb; 21(1):14-8. PubMed ID: 14767901
[TBL] [Abstract][Full Text] [Related]
19. The gene for human protein Z is localized to chromosome 13 at band q34 and is coded by eight regular exons and one alternative exon.
Fujimaki K; Yamazaki T; Taniwaki M; Ichinose A
Biochemistry; 1998 May; 37(19):6838-46. PubMed ID: 9578570
[TBL] [Abstract][Full Text] [Related]
20. Mutation analysis of coding sequences of the entire transforming growth factor beta type II receptor gene in sporadic human colon cancer using genomic DNA and intron primers.
Takenoshita S; Tani M; Nagashima M; Hagiwara K; Bennett WP; Yokota J; Harris CC
Oncogene; 1997 Mar; 14(10):1255-8. PubMed ID: 9121777
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
