BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

276 related articles for article (PubMed ID: 2139713)

  • 1. [Testing of G----A mutation in position 110 of a minor intron of beta-globin genes in patients with thalassemia in Azerbaijan].
    Fedorov AN; Rasulov EM; Oretskaia TS; Lebedeva IV; Ivanovskaia MG; Shabarova ZA; Limborskaia SA
    Mol Gen Mikrobiol Virusol; 1990 Jan; (1):18-22. PubMed ID: 2139713
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Molecular causes of thalassemia. IV. Cloning of the beta-globin gene in a patient with beta-thalassemia from Azerbaijan and determination of the point mutation in a minor intron].
    Limborskaia SA; Bukhman VL; Prosniak MI; Fedorov AN; Slominskiĭ PA
    Genetika; 1987 Feb; 23(2):228-38. PubMed ID: 3030889
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A new mutation in the beta-globin gene (IVS II-850 G-C) found in a Yugoslavian beta-thalassemia heterozygote.
    Jankovic L; Dimovski AJ; Sukarova E; Juricic D; Efremov GD
    Haematologica; 1992; 77(2):119-21. PubMed ID: 1398296
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The spectrum of beta-thalassemia mutations in southern Thailand.
    Nopparatana C; Panich V; Saechan V; Sriroongrueng V; Nopparatana C; Rungjeadpha J; Pornpatkul M; Laosombat V; Fukumaki Y
    Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():229-34. PubMed ID: 8629112
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Molecular genetics of the thalassemias in Argentina].
    Varela V; Rossetti LC; Binaghi A; Targovnik HM; Abreu MS
    Sangre (Barc); 1999 Jun; 44(3):210-5. PubMed ID: 10481583
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [A novel Chinese beta-thalassemia mutation--4bp deletion (AAAC) downstream from the cap site].
    Xu Y
    Zhonghua Yi Xue Za Zhi; 1991 Apr; 71(4):205-7, 16. PubMed ID: 1650632
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [New single point mutation at the initiation codon (ATG-AGG) identified in amplified genomic DNA of a Chinese with beta-thalassaemia].
    Xie S
    Zhonghua Yi Xue Za Zhi; 1990 May; 70(5):258-61, 20. PubMed ID: 1975769
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Study of beta-Thalassemia mutations using the polymerase chain reaction-amplification refractory mutation system and direct DNA sequencing techniques in a group of Egyptian Thalassemia patients.
    El-Gawhary S; El-Shafie S; Niazi M; Aziz M; El-Beshlawy A
    Hemoglobin; 2007; 31(1):63-9. PubMed ID: 17365006
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Analysis of RFLP haplotypes in the beta-globin gene cluster and the identification of beta-thalassemia genes in patients from Guangdong Province].
    Li J
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1992 Feb; 14(1):42-5. PubMed ID: 1350518
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Characterization of beta-thalassaemia mutations using direct genomic sequencing of amplified single copy DNA.
    Wong C; Dowling CE; Saiki RK; Higuchi RG; Erlich HA; Kazazian HH
    Nature; 1987 Nov 26-Dec 2; 330(6146):384-6. PubMed ID: 3683554
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Character of two mutations of the beta-globin gene in beta 0-thalassemia in Azerbaijan].
    Gol'tsov AA; Surin VL; Luk'ianenko AV; Alekseev AA; Kaboev OK; Vinogradov SV; Solov'ev GIa; Berlin IuA; Shvarts EI
    Bioorg Khim; 1989 Jul; 15(7):1001-2. PubMed ID: 2530988
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Analysis of beta-thalassemia mutations and beta-locus control region hypersensitive sites 2, 3 and 4 in southern Thailand.
    Sriroongrueng W; Schleiemacher E; Panich V; Nopparatana C; Saechan V; Laosombat V; Pornpatkul M; Fukumaki Y
    Southeast Asian J Trop Med Public Health; 1997; 28 Suppl 3():120-7. PubMed ID: 9640613
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Molecular causes of thalassemia. III. Molecular genetic variants of beta-thalassemia in Azerbaijan].
    Dergunova LV; Slominskiĭ PA; Rustamov RSh; Dadasheva TS; Amzashvili MG
    Genetika; 1982 Jul; 18(7):1045-55. PubMed ID: 6180957
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Molecular pathology and detection of beta-thalassemias.
    Cao A; Murru S
    Prog Clin Biol Res; 1989; 309():3-11. PubMed ID: 2675099
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A simple non radioactive method for detecting beta-thalassemia/hbe disease: application to prenatal diagnosis.
    Fucharoen S; Fucharoen G; Ratanasiri T; Jetsrisuparb A; Fukumaki Y
    Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():278-81. PubMed ID: 8629124
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Molecular diagnosis of A gamma hereditary persistence of fetal hemoglobin using polymerase chain reaction and oligonucleotide analysis.
    Gottardi E; Alfarano A; Serra A; Sciarratta G; Bertero MT; Saglio G; Camaschella C
    Haematologica; 1990; 75(1):17-20. PubMed ID: 1692560
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Most frequent beta-thalassemia mutations in the Argentinian population].
    Varela V; Abreu S; Rossetti LC; Targovnik H
    Sangre (Barc); 1996 Apr; 41(2):137-40. PubMed ID: 9045354
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Heterogeneity of beta-thalassemia in Azerbaidzhan.
    Dergunova LV; Ryskov AP; Slominsky PA; Rustamov RS; Limborska SA
    Haematologia (Budap); 1984; 17(4):473-81. PubMed ID: 6241915
    [TBL] [Abstract][Full Text] [Related]  

  • 19. "Silent" nucleotide substitution in codon 24 of a beta+ thalassemia globin gene activates splice site in coding sequence RNA.
    Humphries RK; Ley T; Goldsmith ME; Kantor JA; Cline AC; Nienhuis AW
    Prog Clin Biol Res; 1983; 134():123-6. PubMed ID: 6664994
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Silent thalassemias: genotypes and phenotypes.
    Bianco I; Cappabianca MP; Foglietta E; Lerone M; Deidda G; Morlupi L; Grisanti P; Ponzini D; Rinaldi S; Graziani B
    Haematologica; 1997; 82(3):269-80. PubMed ID: 9234571
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.