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 *

188 related articles for article (PubMed ID: 7663000)

  • 1. C to T transition at the first nucleotide of codon 63 of the beta-globin gene corresponding to hemoglobin M-Saskatoon in an Indonesian boy.
    Suryantoro P; Takeshima Y; Haryanto A; Matsuo M
    Jpn J Hum Genet; 1995 Jun; 40(2):195-201. PubMed ID: 7663000
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Dominantly Inherited beta-Thalassemia.
    Efremov GD
    Hemoglobin; 2007; 31(2):193-207. PubMed ID: 17486503
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Two missense mutations in the beta-globin gene can cause severe beta thalassemia. Hemoglobin Medicine Lake (beta 32[B14]leucine-->glutamine; 98 [FG5] valine-->methionine).
    Coleman MB; Lu ZH; Smith CM; Adams JG; Harrell A; Plonczynski M; Steinberg MH
    J Clin Invest; 1995 Feb; 95(2):503-9. PubMed ID: 7860732
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Distinct phenotypic expression associated with a new hyperunstable alpha globin variant (Hb heraklion, alpha1cd37(C2)Pro>0): comparison to other alpha-thalassemic hemoglobinopathies.
    Traeger-Synodinos J; Papassotiriou I; Metaxotou-Mavrommati A; Vrettou C; Stamoulakatou A; Kanavakis E
    Blood Cells Mol Dis; 2000 Aug; 26(4):276-84. PubMed ID: 11042028
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A novel beta-globin structural mutant, Hb Brescia (beta 114 Leu-Pro), causing a severe beta-thalassemia intermedia phenotype.
    Murru S; Poddie D; Sciarratta GV; Agosti S; Baffico M; Melevendi C; Pirastu M; Cao A
    Hum Mutat; 1992; 1(2):124-8. PubMed ID: 1301199
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hb Bleuland [alpha108(G15)Thr-->Asn, ACC-->AAC (alpha2)]: a new abnormal hemoglobin associated with a mild alpha-thalassemia phenotype.
    Harteveld CL; Versteegh FG; Kok PJ; van Rooijen-Nijdam IH; van Delft P; Giordano PC
    Hemoglobin; 2006; 30(3):349-54. PubMed ID: 16840225
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Two different mutations in codon 97 of the beta-globin gene cause Hb Malmö in Sweden.
    Landin B; Berglund S; Wallman K
    Am J Hematol; 1996 Jan; 51(1):32-6. PubMed ID: 8571935
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Hb Niigata [beta1(NA1)Val-->Leu] in a Romanian individual resulting from another nucleotide substitution than that found in the Japanese.
    Moradkhani K; Henthorn J; Riou J; Phelan L; Préhu C; Wajcman H
    Hemoglobin; 2007; 31(4):477-82. PubMed ID: 17994382
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mutational spectrum of delta-globin gene in the Portuguese population.
    Morgado A; Picanço I; Gomes S; Miranda A; Coucelo M; Seuanes F; Seixas MT; Romão L; Faustino P
    Eur J Haematol; 2007 Nov; 79(5):422-8. PubMed ID: 17916081
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Co-inheritance of Hb Pak Num Po, a novel alpha1 gene mutation, and alpha0 thalassemia associated with transfusion-dependent Hb H disease.
    Viprakasit V; Tanphaichitr VS; Veerakul G; Chinchang W; Petrarat S; Pung-Amritt P; Higgs DR
    Am J Hematol; 2004 Mar; 75(3):157-63. PubMed ID: 14978697
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Hb L'Aquila [beta106(G8)Leu-->Val, CTG-->GTG]: a novel thalassemic hemoglobin variant.
    Amato A; Cappabianca MP; Ponzini D; Rinaldi S; Biagio PD; Foglietta E; Grisanti P; Mastropietro F
    Hemoglobin; 2007; 31(3):375-8. PubMed ID: 17654075
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A novel mutation of -73(A-->T) in the CCAAT box of the beta-globin gene identified in a patient with the mild beta-thalassemia intermedia.
    Chen XW; Mo QH; Li Q; Zeng R; Xu XM
    Ann Hematol; 2007 Sep; 86(9):653-7. PubMed ID: 17516066
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Hemoglobin S/hemoglobin Osler: a case with 3 beta globin chains. DNA sequence (AAT) proves that Hb Osler is beta 145 Tyr-->Asn.
    Hutt PJ; Donaldson MH; Khatri J; Fairbanks VF; Hoyer JD; Thibodeau SN; Moxness MS; McMorrow LE; Green MM; Jones RT
    Am J Hematol; 1996 Aug; 52(4):305-9. PubMed ID: 8701949
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Spontaneous mutation of the hemoglobin Leiden (beta 6 or 7 Glu-->0) in a Thai girl.
    Sanguansermsri P; Shimbhu D; Wongvilairat R; Pimsorn C; Sanguansermsri T
    Haematologica; 2003 Dec; 88(12):ECR35. PubMed ID: 14688008
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Molecular analysis of Hb Q-H disease and Hb Q-Hb E in a Singaporean family.
    Tan J; Tay JS; Wong YC; Kham SK; Bte Abd Aziz N; Teo SH; Wong HB
    Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():252-6. PubMed ID: 8629117
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Molecular basis of beta-thalassemia minor in Taiwan.
    Chang JG; Lin CP; Liu TC; Chiou SS; Chen PH; Lee LS; Chen TP
    Int J Hematol; 1994 Jun; 59(4):267-72. PubMed ID: 8086620
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Hb Florida: a novel elongated C-terminal beta-globin variant causing dominant beta-thalassemia phenotype.
    Weinstein BI; Erramouspe B; Albuquerque DM; Oliveira DM; Kimura EM; Costa FF; Sonati MF
    Am J Hematol; 2006 May; 81(5):358-60. PubMed ID: 16628732
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Spectrum of beta-globin gene mutations among thalassemia patients in the West Bank region of Palestine.
    Darwish HM; El-Khatib FF; Ayesh S
    Hemoglobin; 2005; 29(2):119-32. PubMed ID: 15921164
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Hb A2-Pasteur-Tunis [delta59(E3)Lys-->Asn, AAG-->AAC]: a new delta chain variant detected by DNA sequencing in a Tunisian carrier of the codon 39 (C-->T) beta0-Thalassemia mutation.
    Moumni I; Zorai A; Daoued BB; Mosbahi I; Omar S; Kaabachi N; Dellagi K; Abbes S
    Hemoglobin; 2007; 31(1):23-9. PubMed ID: 17365002
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Congenital methemoglobinemia caused by Hb-MRatnagiri (beta-63CAT-->TAT, His-->Tyr) in an Indian family.
    Kedar PS; Nadkarni AH; Phanasgoankar S; Madkaikar M; Ghosh K; Gorakshakar AC; Colah RB; Mohanty D
    Am J Hematol; 2005 Jun; 79(2):168-70. PubMed ID: 15929117
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.