53 related articles for article (PubMed ID: 7686693)
1. A novel polymorphism in glycoprotein IV (replacement of proline-90 by serine) predominates in subjects with platelet GPIV deficiency.
Kashiwagi H; Honda S; Tomiyama Y; Mizutani H; Take H; Honda Y; Kosugi S; Kanayama Y; Kurata Y; Matsuzawa Y
Thromb Haemost; 1993 May; 69(5):481-4. PubMed ID: 7686693
[TBL] [Abstract][Full Text] [Related]
2. Molecular basis of CD36 deficiency. Evidence that a 478C-->T substitution (proline90-->serine) in CD36 cDNA accounts for CD36 deficiency.
Kashiwagi H; Tomiyama Y; Honda S; Kosugi S; Shiraga M; Nagao N; Sekiguchi S; Kanayama Y; Kurata Y; Matsuzawa Y
J Clin Invest; 1995 Mar; 95(3):1040-6. PubMed ID: 7533783
[TBL] [Abstract][Full Text] [Related]
3. Presence of the entire coding region of GP IV mRNA in Nak(a)-negative platelets.
Kashiwagi H; Honda S; Take H; Mizutani H; Imai Y; Furubayashi T; Tomiyama Y; Kurata Y; Yonezawa T
Int J Hematol; 1993 Apr; 57(2):153-61. PubMed ID: 7684270
[TBL] [Abstract][Full Text] [Related]
4. Detection of GPIV (CD36) mRNA in Naka- platelets.
Lipsky RH; Sobieski DA; Tandon NN; Herman J; Ikeda H; Jamieson GA
Thromb Haemost; 1991 Apr; 65(4):456-7. PubMed ID: 1711720
[No Abstract] [Full Text] [Related]
5. Cloning of the cDNA encoding human platelet CD36: comparison to PCR amplified fragments of monocyte, endothelial and HEL cells.
Wyler B; Daviet L; Bortkiewicz H; Bordet JC; McGregor JL
Thromb Haemost; 1993 Sep; 70(3):500-5. PubMed ID: 7505064
[TBL] [Abstract][Full Text] [Related]
6. Platelet membrane protein CD36.
Ikeda H
Hokkaido Igaku Zasshi; 1999 Mar; 74(2):99-104. PubMed ID: 10386159
[TBL] [Abstract][Full Text] [Related]
7. Quantitation of platelet glycoprotein IV (CD36) in healthy subjects and in patients with essential thrombocythemia using an immunocapture assay.
Thibert V; Bellucci S; Edelman L; Tandon NN; Legrand C
Thromb Haemost; 1992 Nov; 68(5):600-5. PubMed ID: 1280864
[TBL] [Abstract][Full Text] [Related]
8. Family studies of type II CD36 deficient subjects: linkage of a CD36 allele to a platelet-specific mRNA expression defect(s) causing type II CD36 deficiency.
Kashiwagi H; Tomiyama Y; Kosugi S; Shiraga M; Lipsky RH; Nagao N; Kanakura Y; Kurata Y; Matsuzawa Y
Thromb Haemost; 1995 Aug; 74(2):758-63. PubMed ID: 8585018
[TBL] [Abstract][Full Text] [Related]
9. Platelet glycoprotein IV (CD36) deficiency is associated with the absence (type I) or the presence (type II) of glycoprotein IV on monocytes.
Yamamoto N; Akamatsu N; Sakuraba H; Yamazaki H; Tanoue K
Blood; 1994 Jan; 83(2):392-7. PubMed ID: 7506948
[TBL] [Abstract][Full Text] [Related]
10. Normal aggregations of glycoprotein IV (CD36)-deficient platelets from seven healthy Japanese donors.
Yamamoto N; Akamatsu N; Yamazaki H; Tanoue K
Br J Haematol; 1992 May; 81(1):86-92. PubMed ID: 1381610
[TBL] [Abstract][Full Text] [Related]
11. Three novel mutations in five unrelated subjects with hereditary protein S deficiency type I.
Reitsma PH; Ploos van Amstel HK; Bertina RM
J Clin Invest; 1994 Feb; 93(2):486-92. PubMed ID: 8113388
[TBL] [Abstract][Full Text] [Related]
12. A resolution of reported discrepancies in the characteristics of platelet glycoproteins IV (GPIV) and IIIb (GPIIIb).
Yamamoto N; de Romeuf C; Tandon NN; Jamieson GA
Thromb Haemost; 1990 Feb; 63(1):97-102. PubMed ID: 1692640
[TBL] [Abstract][Full Text] [Related]
13. [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]
14. T cell signaling abnormalities in systemic lupus erythematosus are associated with increased mutations/polymorphisms and splice variants of T cell receptor zeta chain messenger RNA.
Nambiar MP; Enyedy EJ; Warke VG; Krishnan S; Dennis G; Wong HK; Kammer GM; Tsokos GC
Arthritis Rheum; 2001 Jun; 44(6):1336-50. PubMed ID: 11407693
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. A point mutation associated with leukocyte adhesion deficiency type 1 of moderate severity.
Back AL; Kerkering M; Baker D; Bauer TR; Embree LJ; Hickstein DD
Biochem Biophys Res Commun; 1993 Jun; 193(3):912-8. PubMed ID: 7686755
[TBL] [Abstract][Full Text] [Related]
17. Expression of GPIV and N(aka) antigen on monocytes in N(aka)-negative subjects whose platelets lack GPIV.
Take H; Kashiwagi H; Tomiyama Y; Honda S; Honda Y; Mizutani H; Furubayashi T; Karasuno T; Nishiura T; Kanayama Y
Br J Haematol; 1993 Jul; 84(3):387-91. PubMed ID: 7692927
[TBL] [Abstract][Full Text] [Related]
18. A single nucleotide insertion in codon 317 of the CD36 gene leads to CD36 deficiency.
Kashiwagi H; Tomiyama Y; Nozaki S; Honda S; Kosugi S; Shiraga M; Nakagawa T; Nagao N; Kanakura Y; Kurata Y; Matsuzawa Y
Arterioscler Thromb Vasc Biol; 1996 Aug; 16(8):1026-32. PubMed ID: 8696942
[TBL] [Abstract][Full Text] [Related]
19. Dauricine inhibits redistribution of platelet membrane glycoprotein IV and release of intracellular alpha-granule thrombospondin induced by thrombin.
Guo T; Zhang YZ; Liu DX; Zou P; Shen D
Zhongguo Yao Li Xue Bao; 1999 Jun; 20(6):533-6. PubMed ID: 10678148
[TBL] [Abstract][Full Text] [Related]
20. Identification of a homozygous single base pair deletion in the gene coding for the human platelet glycoprotein Ib alpha causing Bernard-Soulier syndrome.
Simsek S; Admiraal LG; Modderman PW; van der Schoot CE; von dem Borne AE
Thromb Haemost; 1994 Sep; 72(3):444-9. PubMed ID: 7855797
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]