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 *

117 related articles for article (PubMed ID: 8690922)

  • 61. Characterization of complement C6 deficiency in a PVG/c rat strain.
    van Dixhoorn MG; Timmerman JJ; Van Gijlswijk-Janssen DJ; Muizert Y; Verweij C; Discipio RG; Daha MR
    Clin Exp Immunol; 1997 Aug; 109(2):387-96. PubMed ID: 9276537
    [TBL] [Abstract][Full Text] [Related]  

  • 62. Mutations in exon 3 of the glycogen debranching enzyme gene are associated with glycogen storage disease type III that is differentially expressed in liver and muscle.
    Shen J; Bao Y; Liu HM; Lee P; Leonard JV; Chen YT
    J Clin Invest; 1996 Jul; 98(2):352-7. PubMed ID: 8755644
    [TBL] [Abstract][Full Text] [Related]  

  • 63. Simultaneous occurrence of hereditary C6 and C2 deficiency in a French-Canadian family.
    Delâge JM; Lehner-Netsch G; Lafleur R; Simard J; Brun G; Prochazka E
    Immunology; 1979 Jun; 37(2):419-28. PubMed ID: 468307
    [TBL] [Abstract][Full Text] [Related]  

  • 64. Six missense mutations associated with type I and type II protein C deficiency and implications obtained from molecular modelling.
    Zheng YZ; Sakata T; Matsusue T; Umeyama H; Kato H; Miyata T
    Blood Coagul Fibrinolysis; 1994 Oct; 5(5):687-96. PubMed ID: 7865674
    [TBL] [Abstract][Full Text] [Related]  

  • 65. Moyamoya Disease Associated with a Deficiency of Complement Component 6.
    Kato M; Kudo Y; Hatase M; Tsuchida N; Takeyama S; Sugiyama T; Fujimura M; Yabe I; Tsujimoto H; Fukumori Y; Inoue N; Atsumi T
    J Stroke Cerebrovasc Dis; 2022 Aug; 31(8):106601. PubMed ID: 35717718
    [TBL] [Abstract][Full Text] [Related]  

  • 66. Complement component C5 and C6 mutation screening indicated in meningococcal disease in South Africa.
    Owen EP; Leisegang F; Whitelaw A; Simpson J; Baker S; Würzner R; Potter P; Orren A
    S Afr Med J; 2012 May; 102(6):525-7. PubMed ID: 22668955
    [TBL] [Abstract][Full Text] [Related]  

  • 67. High frequencies in African and non-African populations of independent mutations in the mannose binding protein gene.
    Lipscombe RJ; Sumiya M; Hill AV; Lau YL; Levinsky RJ; Summerfield JA; Turner MW
    Hum Mol Genet; 1992 Dec; 1(9):709-15. PubMed ID: 1304173
    [TBL] [Abstract][Full Text] [Related]  

  • 68. Familial hypercholesterolemia. Acceptor splice site (G-->C) mutation in intron 7 of the LDL-R gene: alternate RNA editing causes exon 8 skipping or a premature stop codon in exon 8. LDL-R(Honduras-1) [LDL-R1061(-1) G-->C].
    Yu L; Heere-Ress E; Boucher B; Defesche JC; Kastelein J; Lavoie MA; Genest J
    Atherosclerosis; 1999 Sep; 146(1):125-31. PubMed ID: 10487495
    [TBL] [Abstract][Full Text] [Related]  

  • 69. Genetic analysis of the HPRT mutation of Lesch-Nyhan syndrome in a Chinese family.
    Lee WJ; Lee HM; Chi CS; Yang MT; Lin HY; Lin WH
    Zhonghua Yi Xue Za Zhi (Taipei); 1995 Dec; 56(6):359-66. PubMed ID: 8851475
    [TBL] [Abstract][Full Text] [Related]  

  • 70. Hereditary protein C deficiency associated with mutations in exon IX of the protein C gene.
    Doig RG; Begley CG; McGrath KM
    Thromb Haemost; 1994 Aug; 72(2):203-8. PubMed ID: 7831652
    [TBL] [Abstract][Full Text] [Related]  

  • 71. Detection of heterozygous mutations in the RB1 gene in retinoblastoma patients using single-strand conformation polymorphism analysis and polymerase chain reaction sequencing.
    Hogg A; Onadim Z; Baird PN; Cowell JK
    Oncogene; 1992 Jul; 7(7):1445-51. PubMed ID: 1352398
    [TBL] [Abstract][Full Text] [Related]  

  • 72. NF1 gene mutations in Japanese with neurofibromatosis 1 (NF1).
    Hatta N; Horiuchi T; Watanabe I; Kobayashi Y; Shirakata Y; Ohtsuka H; Minami T; Ueda K; Kokoroishi T; Fujita S
    Biochem Biophys Res Commun; 1995 Jul; 212(2):697-704. PubMed ID: 7542886
    [TBL] [Abstract][Full Text] [Related]  

  • 73. High sensitivity of the single-strand conformation polymorphism method for detecting sequence variations in the low-density lipoprotein receptor gene validated by DNA sequencing.
    Jensen HK; Jensen LG; Hansen PS; Faergeman O; Gregersen N
    Clin Chem; 1996 Aug; 42(8 Pt 1):1140-6. PubMed ID: 8697568
    [TBL] [Abstract][Full Text] [Related]  

  • 74. Molecular cloning of the C6A form cDNA of the mouse sixth complement component: functional integrity despite the absence of factor I modules.
    Yu JX; Bradt BM; Cooper NR
    Immunogenetics; 2000 Aug; 51(10):779-87. PubMed ID: 10970092
    [TBL] [Abstract][Full Text] [Related]  

  • 75. Clinical presentations and molecular basis of complement C1r deficiency in a male African-American patient with systemic lupus erythematosus.
    Wu YL; Brookshire BP; Verani RR; Arnett FC; Yu CY
    Lupus; 2011 Oct; 20(11):1126-34. PubMed ID: 21784777
    [TBL] [Abstract][Full Text] [Related]  

  • 76. A new compound heterozygous mutation (W17X, 436 + 5G --> T) in the cytochrome P450c17 gene causes 17 alpha-hydroxylase/17,20-lyase deficiency.
    Suzuki Y; Nagashima T; Nomura Y; Onigata K; Nagashima K; Morikawa A
    J Clin Endocrinol Metab; 1998 Jan; 83(1):199-202. PubMed ID: 9435441
    [TBL] [Abstract][Full Text] [Related]  

  • 77. HLA-G exhibits low level of polymorphism in indigenous East Africans.
    Matte C; Lacaille J; Zijenah L; Ward B; Roger M;
    Hum Immunol; 2002 Jun; 63(6):495-501. PubMed ID: 12039526
    [TBL] [Abstract][Full Text] [Related]  

  • 78. Structure of the human C7 gene and comparison with the C6, C8A, C8B, and C9 genes.
    Hobart MJ; Fernie BA; DiScipio RG
    J Immunol; 1995 May; 154(10):5188-94. PubMed ID: 7730625
    [TBL] [Abstract][Full Text] [Related]  

  • 79. DNA polymorphisms of the complement C6 and C7 genes.
    Fernie BA; Würzner R; Unsworth DJ; Tuxworth RI; Hobart MJ
    Ann Hum Genet; 1995 Apr; 59(2):163-81. PubMed ID: 7625764
    [TBL] [Abstract][Full Text] [Related]  

  • 80. Two novel partial deletions of LDL-receptor gene in Italian patients with familial hypercholesterolemia (FH Siracusa and FH Reggio Emilia).
    Garuti R; Lelli N; Barozzini M; Tiozzo R; Ghisellini M; Simone ML; Li Volti S; Garozzo R; Mollica F; Vergoni W; Bertolini S; Calandra S
    Atherosclerosis; 1996 Mar; 121(1):105-17. PubMed ID: 8678915
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.