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 *

54 related articles for article (PubMed ID: 7689618)

  • 21. A compound heterozygous protein C deficiency with a single nucleotide G deletion encoding Gly-381 and an amino acid substitution of Lys for Gla-26.
    Ido M; Ohiwa M; Hayashi T; Nishioka J; Hatada T; Watanabe Y; Wada H; Shirakawa S; Suzuki K
    Thromb Haemost; 1993 Oct; 70(4):636-41. PubMed ID: 8115990
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Antigenic alteration of an anomalous human luteinizing hormone caused by two chorionic gonadotropin-type amino-acid substitutions.
    Okuda K; Yamada T; Imoto H; Komatsubara H; Sugimoto O
    Biochem Biophys Res Commun; 1994 Apr; 200(1):584-90. PubMed ID: 8166733
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Conformational changes of gp120 in epitopes near the CCR5 binding site are induced by CD4 and a CD4 miniprotein mimetic.
    Zhang W; Canziani G; Plugariu C; Wyatt R; Sodroski J; Sweet R; Kwong P; Hendrickson W; Chaiken I
    Biochemistry; 1999 Jul; 38(29):9405-16. PubMed ID: 10413516
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Passage of HIV-1 molecular clones into different cell lines confers differential sensitivity to neutralization.
    Zhang YJ; Fredriksson R; McKeating JA; Fenyö EM
    Virology; 1997 Nov; 238(2):254-64. PubMed ID: 9400598
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Molecular genetics of hereditary prothrombin deficiency in Indian patients: identification of a novel Ala362 --> Thr (Prothrombin Vellore 1) mutation.
    Jayandharan G; Viswabandya A; Baidya S; Nair SC; Shaji RV; Chandy M; Srivastava A
    J Thromb Haemost; 2005 Jul; 3(7):1446-53. PubMed ID: 15892853
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Detection of T cell CD4 epitopes in HIV-infected individuals.
    Kunkl A; Valle MT; Fenoglio D; Dodi F; Morandi N; Rizzo F; Manca F
    Eur J Histochem; 1994; 38 Suppl 1():41-6. PubMed ID: 8547709
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. Recognition of T cell epitopes unique to Cha o 2, the major allergen in Japanese cypress pollen, in allergic patients cross-reactive to Japanese cedar and Japanese cypress pollen.
    Sone T; Dairiki K; Morikubo K; Shimizu K; Tsunoo H; Mori T; Kino K
    Allergol Int; 2009 Jun; 58(2):237-45. PubMed ID: 19307778
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Inherited OKT4 epitope deficiency in a Chinese rhesus macaque.
    Liu BB; Zhao ML; Wang Y; Hu ZF; Zheng YT; Tian RR
    J Med Primatol; 2021 Jun; 50(3):185-188. PubMed ID: 33893743
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Alpha (1,3/1,4)fucosyltransferase (FucT-III) gene is inactivated by a single amino acid substitution in Lewis histo-blood type negative individuals.
    Nishihara S; Yazawa S; Iwasaki H; Nakazato M; Kudo T; Ando T; Narimatsu H
    Biochem Biophys Res Commun; 1993 Oct; 196(2):624-31. PubMed ID: 8240337
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Molecular basis of intermittent maple syrup urine disease: novel mutations in the E2 gene of the branched-chain alpha-keto acid dehydrogenase complex.
    Tsuruta M; Mitsubuchi H; Mardy S; Miura Y; Hayashida Y; Kinugasa A; Ishitsu T; Matsuda I; Indo Y
    J Hum Genet; 1998; 43(2):91-100. PubMed ID: 9621512
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Biological activities on T lymphocytes of a baculovirus-expressed chimeric recombinant IgG1 antibody with specificity for the CDR3-like loop on the D1 domain of the CD4 molecule.
    Troadec S; Bès C; Chentouf M; Nguyen B; Briant L; Jacquet C; Chebli K; Pugnière M; Roquet F; Cerutti M; Chardès T
    Clin Immunol; 2006 Apr; 119(1):38-50. PubMed ID: 16426893
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A single amino acid substitution in a common African allele of the CD4 molecule ablates binding of the monoclonal antibody, OKT4.
    Lederman S; DeMartino JA; Daugherty BL; Foeldvari I; Yellin MJ; Cleary AM; Berkowitz N; Lowy I; Braunstein NS; Mark GE
    Mol Immunol; 1991 Nov; 28(11):1171-81. PubMed ID: 1961196
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Novel double heterozygous mutations on Met306Val and Thr181Asn related to a hereditary coagulation factor VII deficiency].
    Tu CQ; Deng CY; Wu JZ; Pan CY; Xie CY
    Zhonghua Yi Xue Za Zhi; 2006 Jan; 86(2):124-7. PubMed ID: 16620721
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Heterogeneity of epitopes of the CD4 molecule in a female patient with idiopathic pulmonary fibrosis].
    Famularo G; Giacomelli R; Tonietti G
    Medicina (Firenze); 1989; 9(3):279-80. PubMed ID: 2482402
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Flow cytometry analysis of OKT4 epitope deficiency in South African black children.
    Hughes EJ; Goddard EA; Bouic P; Beatty DW
    Clin Exp Immunol; 1994 Dec; 98(3):526-31. PubMed ID: 7527746
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Single amino acid substitution in the V3 domain of CD4 is responsible for OKT4 epitope deficiency.
    Tokito S; Kishi S; Yamamoto R; Takenaka T; Nakauchi H
    Immunogenetics; 1991; 34(3):208-10. PubMed ID: 1716607
    [No Abstract]   [Full Text] [Related]  

  • 38. Human monocyte antigens in a random sample from Japan.
    Nagai T; Sugita Y; Kurihara M; Ikeda T; Rose M
    Exp Clin Immunogenet; 1991; 8(2):115-8. PubMed ID: 1789991
    [TBL] [Abstract][Full Text] [Related]  

  • 39. OKT4 epitope deficiency and symptomatic immune impairment.
    Van de Perre P; Lepage P
    AIDS; 1989 Jul; 3(7):461. PubMed ID: 2475146
    [No Abstract]   [Full Text] [Related]  

  • 40. Familial OKT4+ lymphocyte deficiency.
    Amino N; Aozasa M; Iwatani Y; Tamaki H; Miyai K; Sato H; Gunji T
    Lancet; 1984 Jul; 2(8394):94-5. PubMed ID: 6204180
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 3.