These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

165 related articles for article (PubMed ID: 10754001)

  • 1. Linkage of familial moyamoya disease (spontaneous occlusion of the circle of Willis) to chromosome 17q25.
    Yamauchi T; Tada M; Houkin K; Tanaka T; Nakamura Y; Kuroda S; Abe H; Inoue T; Ikezaki K; Matsushima T; Fukui M
    Stroke; 2000 Apr; 31(4):930-5. PubMed ID: 10754001
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Sequence analysis and bioinformatics analysis of chromosome 17q25 in familial moyamoya disease.
    Nanba R; Tada M; Kuroda S; Houkin K; Iwasaki Y
    Childs Nerv Syst; 2005 Jan; 21(1):62-8. PubMed ID: 15340753
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Autosomal dominant moyamoya disease maps to chromosome 17q25.3.
    Mineharu Y; Liu W; Inoue K; Matsuura N; Inoue S; Takenaka K; Ikeda H; Houkin K; Takagi Y; Kikuta K; Nozaki K; Hashimoto N; Koizumi A
    Neurology; 2008 Jun; 70(24 Pt 2):2357-63. PubMed ID: 18463369
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A novel susceptibility locus for moyamoya disease on chromosome 8q23.
    Sakurai K; Horiuchi Y; Ikeda H; Ikezaki K; Yoshimoto T; Fukui M; Arinami T
    J Hum Genet; 2004; 49(5):278-81. PubMed ID: 15362573
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Preliminary linkage analysis of a Chinese family with benign familial infantile convulsion].
    Xiong G; Deng FY; Xiao B; Yang XS; Ning JC; Wu ZG; Wang K; Deng HW
    Zhonghua Er Ke Za Zhi; 2004 Jun; 42(6):424-8. PubMed ID: 15265426
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mapping of a familial moyamoya disease gene to chromosome 3p24.2-p26.
    Ikeda H; Sasaki T; Yoshimoto T; Fukui M; Arinami T
    Am J Hum Genet; 1999 Feb; 64(2):533-7. PubMed ID: 9973290
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Linkage analysis of moyamoya disease on chromosome 6.
    Inoue TK; Ikezaki K; Sasazuki T; Matsushima T; Fukui M
    J Child Neurol; 2000 Mar; 15(3):179-82. PubMed ID: 10757474
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Linkage of Gordon's syndrome to the long arm of chromosome 17 in a region recently linked to familial essential hypertension.
    O'Shaughnessy KM; Fu B; Johnson A; Gordon RD
    J Hum Hypertens; 1998 Oct; 12(10):675-8. PubMed ID: 9819014
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A susceptibility locus for epidermodysplasia verruciformis, an abnormal predisposition to infection with the oncogenic human papillomavirus type 5, maps to chromosome 17qter in a region containing a psoriasis locus.
    Ramoz N; Rueda LA; Bouadjar B; Favre M; Orth G
    J Invest Dermatol; 1999 Mar; 112(3):259-63. PubMed ID: 10084299
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Isolated familial somatotropinomas: establishment of linkage to chromosome 11q13.1-11q13.3 and evidence for a potential second locus at chromosome 2p16-12.
    Gadelha MR; Une KN; Rohde K; Vaisman M; Kineman RD; Frohman LA
    J Clin Endocrinol Metab; 2000 Feb; 85(2):707-14. PubMed ID: 10690880
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genetic homogeneity for inherited congenital microcoria loci in an Asian Indian pedigree.
    Ramprasad VL; Sripriya S; Ronnie G; Nancarrow D; Saxena S; Hemamalini A; Kumar D; Vijaya L; Kumaramanickavel G
    Mol Vis; 2005 Nov; 11():934-40. PubMed ID: 16288197
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Age-related maculopathy: an expanded genome-wide scan with evidence of susceptibility loci within the 1q31 and 17q25 regions.
    Weeks DE; Conley YP; Tsai HJ; Mah TS; Rosenfeld PJ; Paul TO; Eller AW; Morse LS; Dailey JP; Ferrell RE; Gorin MB
    Am J Ophthalmol; 2001 Nov; 132(5):682-92. PubMed ID: 11704029
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mapping of the familial infantile myasthenia (congenital myasthenic syndrome type Ia) gene to chromosome 17p with evidence of genetic homogeneity.
    Christodoulou K; Tsingis M; Deymeer F; Serdaroglu P; Ozdemir C; Al-Shehab A; Bairactaris C; Mavromatis I; Mylonas I; Evoli A; Kyriallis K; Middleton LT
    Hum Mol Genet; 1997 Apr; 6(4):635-40. PubMed ID: 9097970
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Evidence for linkage of the gene causing familial Mediterranean fever to chromosome 17q in non-Ashkenazi Jewish families: second locus or type I error?
    Aksentijevich I; Gruberg L; Pras E; Balow JE; Kovo M; Gazit E; Dean M; Pras M; Kastner DL
    Hum Genet; 1993 Jul; 91(6):527-34. PubMed ID: 8340105
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Evidence for a nonallelic heterogeneity of epidermodysplasia verruciformis with two susceptibility loci mapped to chromosome regions 2p21-p24 and 17q25.
    Ramoz N; Taïeb A; Rueda LA; Montoya LS; Bouadjar B; Favre M; Orth G
    J Invest Dermatol; 2000 Jun; 114(6):1148-53. PubMed ID: 10844558
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Assignment of two loci for autosomal dominant adolescent idiopathic scoliosis to chromosomes 9q31.2-q34.2 and 17q25.3-qtel.
    Ocaka L; Zhao C; Reed JA; Ebenezer ND; Brice G; Morley T; Mehta M; O'Dowd J; Weber JL; Hardcastle AJ; Child AH
    J Med Genet; 2008 Feb; 45(2):87-92. PubMed ID: 17932119
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Hereditary neuralgic amyotrophy: evidence for genetic homogeneity and mapping to chromosome 17q25.
    Pellegrino JE; George RA; Biegel J; Farlow MR; Gardner K; Caress J; Brown MJ; Rebbeck TR; Bird TD; Chance PF
    Hum Genet; 1997 Dec; 101(3):277-83. PubMed ID: 9439655
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A novel locus for Leber congenital amaurosis (LCA4) with anterior keratoconus mapping to chromosome 17p13.
    Hameed A; Khaliq S; Ismail M; Anwar K; Ebenezer ND; Jordan T; Mehdi SQ; Payne AM; Bhattacharya SS
    Invest Ophthalmol Vis Sci; 2000 Mar; 41(3):629-33. PubMed ID: 10711674
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Suggestive linkage of familial primary cutaneous amyloidosis to a locus on chromosome 1q23.
    Lin MW; Lee DD; Lin CH; Huang CY; Wong CK; Chang YT; Liu HN; Hsiao KJ; Tsai SF
    Br J Dermatol; 2005 Jan; 152(1):29-36. PubMed ID: 15656797
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Linkage analysis of candidate genes in autoimmune thyroid disease. III. Detailed analysis of chromosome 14 localizes Graves' disease-1 (GD-1) close to multinodular goiter-1 (MNG-1). International Consortium for the Genetics of Autoimmune Thyroid Disease.
    Tomer Y; Barbesino G; Greenberg DA; Concepcion E; Davies TF
    J Clin Endocrinol Metab; 1998 Dec; 83(12):4321-7. PubMed ID: 9851771
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.