BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

93 related articles for article (PubMed ID: 9449702)

  • 21. 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]  

  • 22. Articular, monoclonal gamma3 heavy-chain deposition disease: characterization of a partially deleted heavy-chain gene and its protein product synthesized in vivo and in vitro.
    Thompson KM; Sletten K; Brandtzaeg P; Källberg E; Wien TN; Husby G
    Arthritis Rheum; 2003 Nov; 48(11):3266-71. PubMed ID: 14613292
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Analysis, identification and correction of some errors of model refseqs appeared in NCBI Human Gene Database by in silico cloning and experimental verification of novel human genes].
    Zhang DL; Ji L; Li YD
    Yi Chuan Xue Bao; 2004 May; 31(5):431-43. PubMed ID: 15478601
    [TBL] [Abstract][Full Text] [Related]  

  • 24. An SP-B gene mutation responsible for SP-B deficiency in fatal congenital alveolar proteinosis: evidence for a mutation hotspot in exon 4.
    Lin Z; deMello DE; Wallot M; Floros J
    Mol Genet Metab; 1998 May; 64(1):25-35. PubMed ID: 9682215
    [TBL] [Abstract][Full Text] [Related]  

  • 25. The human antibody response to porcine xenoantigens is encoded by IGHV3-11 and IGHV3-74 IgVH germline progenitors.
    Kearns-Jonker M; Swensson J; Ghiuzeli C; Chu W; Osame Y; Starnes V; Cramer DV
    J Immunol; 1999 Oct; 163(8):4399-412. PubMed ID: 10510381
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Analysis of Ig subclass deficiency: First reported case of IgG2, IgG4, and IgA deficiency caused by deletion of C alpha 1, psi C gamma, C gamma 2, C gamma 4, and C epsilon in a Mongoloid patient.
    Terada T; Kaneko H; Li AL; Kasahara K; Ibe M; Yokota S; Kondo N
    J Allergy Clin Immunol; 2001 Oct; 108(4):602-6. PubMed ID: 11590388
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Gene deletion as a cause of associated deficiency of IgA1, IgG2, IgG4 and IgE.
    Plebani A; Carbonara AO; Bottaro A; Gallina R; Boccazzi C; Crispino P; Ruggeri L; Salvioni F; Duina M; Negrini A
    Immunodeficiency; 1993; 4(1-4):245-8. PubMed ID: 8167710
    [No Abstract]   [Full Text] [Related]  

  • 28. Growth hormone insensitivity and severe short stature in siblings: a novel mutation at the exon 13-intron 13 junction of the STAT5b gene.
    Hwa V; Camacho-Hübner C; Little BM; David A; Metherell LA; El-Khatib N; Savage MO; Rosenfeld RG
    Horm Res; 2007; 68(5):218-24. PubMed ID: 17389811
    [TBL] [Abstract][Full Text] [Related]  

  • 29. One novel and one recurrent mutation in the PROS1 gene cause type I protein S deficiency in patients with pulmonary embolism associated with deep vein thrombosis.
    Mizukami K; Nakabayashi T; Naitoh S; Takeda M; Tarumi T; Mizoguchi I; Ieko M; Koike T
    Am J Hematol; 2006 Oct; 81(10):787-97. PubMed ID: 16868938
    [TBL] [Abstract][Full Text] [Related]  

  • 30. NF-kappaB elements associated with the Stat6 site in the germline gamma1 immunoglobulin promoter are not necessary for the transcriptional response to CD40 ligand.
    Berton MT; Linehan LA; Wick KR; Dunnick WA
    Int Immunol; 2004 Dec; 16(12):1741-9. PubMed ID: 15504762
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Transcript mapping of the human chromosome 11q12-q13.1 gene-rich region identifies several newly described conserved genes.
    Cooper PR; Nowak NJ; Higgins MJ; Church DM; Shows TB
    Genomics; 1998 May; 49(3):419-29. PubMed ID: 9615227
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Serum levels of IgG subclasses and vitamin A in children with recurrent respiratory tract infection].
    Qian L; Lu JR
    Zhongguo Dang Dai Er Ke Za Zhi; 2007 Dec; 9(6):557-8. PubMed ID: 18082039
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Gene segments encoding membrane domains of the human immunoglobulin gamma 3 and alpha chains.
    Bensmana M; Lefranc MP
    Immunogenetics; 1990; 32(5):321-30. PubMed ID: 1979064
    [TBL] [Abstract][Full Text] [Related]  

  • 34. IgG2 deficiency and intractable epilepsy of childhood.
    Duse M; Tiberti S; Plebani A; Avanzini MA; Gardenghi M; Menegati E; Monafo V; Ugazio AG
    Monogr Allergy; 1986; 20():128-34. PubMed ID: 3773903
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A novel monospecific IgG2/lambda-autoantibody with specificity for a mitochondrial antigen: evidence for an antigen-driven pathogenetic B-cell response in rheumatoid synovial tissue, induced by tissue alteration.
    Krenn V; Molitoris R; Berek C; Sack U; König A; Müller-Deubert S; Kempf V; Mosgoeller W; Kerkau T; Vollmers HP; Müller-Hermelink HK
    Lab Invest; 1998 Apr; 78(4):485-96. PubMed ID: 9564893
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Immunological evaluation of allergic respiratory children with recurrent sinusitis.
    Costa Carvalho BT; Nagao AT; Arslanian C; Carneiro Sampaio MM; Naspitz CK; Sorensen RU; Leiva L; Solé D
    Pediatr Allergy Immunol; 2005 Sep; 16(6):534-8. PubMed ID: 16176402
    [TBL] [Abstract][Full Text] [Related]  

  • 37. IgG2 deficiency associated with defects in production of interferon-gamma; comparison with common variable immunodeficiency.
    Inoue R; Kondo N; Kobayashi Y; Fukutomi O; Orii T
    Scand J Immunol; 1995 Feb; 41(2):130-4. PubMed ID: 7863259
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Molecular and functional analysis of SLC25A20 mutations causing carnitine-acylcarnitine translocase deficiency.
    Iacobazzi V; Invernizzi F; Baratta S; Pons R; Chung W; Garavaglia B; Dionisi-Vici C; Ribes A; Parini R; Huertas MD; Roldan S; Lauria G; Palmieri F; Taroni F
    Hum Mutat; 2004 Oct; 24(4):312-20. PubMed ID: 15365988
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [IgG2 deficiency associated with recurrent pneumonia and asthma (review of an IgG subclass)].
    de José Gomez MI; González de Dios J; Hernando de Larramendi C; Jiménez García A; Vidal López ML; García Hortelano J
    An Esp Pediatr; 1990 Sep; 33(3):258-64. PubMed ID: 2285191
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Reduced expression of the interferon-gamma messenger RNA in IgG2 deficiency.
    Kondo N; Inoue R; Kasahara K; Fukao T; Kaneko H; Tashita H; Teramoto T
    Scand J Immunol; 1997 Feb; 45(2):227-30. PubMed ID: 9042436
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.