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 *

119 related articles for article (PubMed ID: 7474437)

  • 21. Plasminogen with type-I mutation is polymorphic in the Japanese population.
    Kikuchi S; Yamanouchi Y; Li L; Kobayashi K; Ijima H; Miyazaki R; Tsuchiya S; Hamaguchi H
    Hum Genet; 1992; 90(1-2):7-11. PubMed ID: 1427790
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Detection of the plasma cholinesterase K variant by PCR using an amplification-created restriction site.
    Jensen FS; Nielsen LR; Schwartz M
    Hum Hered; 1996; 46(1):26-31. PubMed ID: 8825459
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Two mutations in exon XII of the protein S alpha gene in four thrombophilic families resulting in premature stop codons and depressed levels of mutated mRNA.
    Andersen BD; Lind B; Philips M; Hansen AB; Ingerslev J; Thorsen S
    Thromb Haemost; 1996 Aug; 76(2):143-50. PubMed ID: 8865520
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Missense mutations of the butyrylcholinesterase gene in six Japanese patients with low cholinesterasemia: genetic analysis using sera stored in a freezer].
    Hidaka K; Watanabe Y; Ueda N; Tomita M; Higashi M; Abe K; Minatogawa Y; Iuchi I
    Rinsho Byori; 1999 Oct; 47(10):980-2. PubMed ID: 10590675
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [4 families with silent cholinesterase variant].
    Moreno Monedero MJ; Acevedo León D; Caballero Ramón S; Vidal Martínez J; Moral Baltuille A; Perales Tortosa G; Casas Terrón E; Gil Minguillón C
    Rev Esp Anestesiol Reanim; 1990; 37(3):164-7. PubMed ID: 2389078
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Seven novel mutations in the long isoform of the USH2A gene in Chinese families with nonsyndromic retinitis pigmentosa and Usher syndrome Type II.
    Xu W; Dai H; Lu T; Zhang X; Dong B; Li Y
    Mol Vis; 2011; 17():1537-52. PubMed ID: 21686329
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Genetic epidemiology of hereditary hemorrhagic telangiectasia in a local community in the northern part of Japan.
    Dakeishi M; Shioya T; Wada Y; Shindo T; Otaka K; Manabe M; Nozaki J; Inoue S; Koizumi A
    Hum Mutat; 2002 Feb; 19(2):140-8. PubMed ID: 11793473
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Mutation analysis of keratin 9 gene in a pedigree with epidermolytic palmoplantar keratoderma].
    Zhang BR; Yin XZ; Xia K; Ding MP; Hu ZM; Zheng M; Liu ZR; Xia JH
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Dec; 21(6):570-3. PubMed ID: 15583984
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Detection of ciprofloxacin resistance mutations in Campylobacter jejuni gyrA by nonradioisotopic single-strand conformation polymorphism and direct DNA sequencing.
    Charvalos E; Peteinaki E; Spyridaki I; Manetas S; Tselentis Y
    J Clin Lab Anal; 1996; 10(3):129-33. PubMed ID: 8731499
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Four novel gene mutations in five Japanese male patients with neonatal or late onset OTC deficiency: application of PCR-single-strand conformation polymorphisms for all exons and adjacent introns [corrected].
    Matsuura T; Hoshide R; Setoyama C; Shimada K; Hase Y; Yanagawa T; Kajita M; Matsuda I
    Hum Genet; 1993 Aug; 92(1):49-56. PubMed ID: 8365726
    [TBL] [Abstract][Full Text] [Related]  

  • 31. The COL4A5 gene in Japanese Alport syndrome patients: spectrum of mutations of all exons. The Japanese Alport Network.
    Kawai S; Nomura S; Harano T; Harano K; Fukushima T; Osawa G
    Kidney Int; 1996 Mar; 49(3):814-22. PubMed ID: 8648925
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A variant serum cholinesterase and a confirmed point mutation at Gly-365 to Arg found in a patient with liver cirrhosis.
    Hada T; Muratani K; Ohue T; Imanishi H; Moriwaki Y; Itoh M; Amuro Y; Higashino K
    Intern Med; 1992 Mar; 31(3):357-62. PubMed ID: 1611188
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Silent cholinesterase gene: three homozygotes in a small Caucasian population.
    Santoro P; Lucci A; Tardi C
    Boll Soc Ital Biol Sper; 1992 Mar; 68(3):187-94. PubMed ID: 1389075
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [A family of pseudocholinesterase deficiency (silent type II)].
    Yokota H; Toyota S; Ohkubo S; Kamei S; Uchimura H; Okubo A; Houzumi M; Sudo K; Sakamoto Y
    Rinsho Byori; 1989 Oct; 37(10):1177-80. PubMed ID: 2601076
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Immunological studies of families segregating the silent gene for plasma cholinesterase.
    Whittaker M; Jones JW; Braven J
    Hum Hered; 1991; 41(2):77-83. PubMed ID: 1855785
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Molecular characterization of beta-thalassemia in Czechoslovakia.
    Indrak K; Brabec V; Indrakova J; Chrobak L; Sakalova A; Jarosova M; Cermak J; Fei YJ; Kutlar F; Gu YC
    Hum Genet; 1992 Feb; 88(4):399-404. PubMed ID: 1740317
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Genetic diagnosis of phenylketonuria: identification of the mutations of phenylalanine hydroxylase gene by PCR direct sequencing].
    Yamashita K; Takarada Y; Otsuka N; Kagawa S; Matsuoka A; Kalanin J
    Rinsho Byori; 1992 Oct; 40(10):1060-6. PubMed ID: 1307609
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Identification of a novel mutation of GALNS gene from a Chinese pedigree with mucopolysaccharidosis type IV A].
    Zhao Y; Meng YX; Guo YB; Du ML; Ai Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Jun; 28(3):241-6. PubMed ID: 21644215
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Identification of novel mutations in WISP3 gene in two unrelated Chinese families with progressive pseudorheumatoid dysplasia.
    Yue H; Zhang ZL; He JW
    Bone; 2009 Apr; 44(4):547-54. PubMed ID: 19064006
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Splicing defect of the glycoasparaginase gene in two Japanese siblings with apartylglucosaminuria.
    Yoshida K; Yanagisawa N; Oshima A; Sakuraba H; Iida Y; Suzuki Y
    Hum Genet; 1992; 90(1-2):179-80. PubMed ID: 1427775
    [TBL] [Abstract][Full Text] [Related]  

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