164 related articles for article (PubMed ID: 17292081)
1. Structural analysis on the abnormal elongated hemoglobin "hemoglobin Geneva".
Wiwanitkit V
Nanomedicine; 2005 Sep; 1(3):216-8. PubMed ID: 17292081
[TBL] [Abstract][Full Text] [Related]
2. Secondary and tertiary structure aberration of alpha globin chain in haemoglobin Q-India disorder.
Wiwanitkit V
Indian J Pathol Microbiol; 2006 Oct; 49(4):491-4. PubMed ID: 17183835
[TBL] [Abstract][Full Text] [Related]
3. Modeling for tertiary structure of globin chain in Hemoglobin Suan-Dok disorder.
Wiwanitkit V
Hematology; 2005 Apr; 10(2):163-5. PubMed ID: 16019464
[TBL] [Abstract][Full Text] [Related]
4. Tertiary structural analysis of the elongated part of an abnormal hemoglobin, hemoglobin Pakse.
Wiwanitkit V
Int J Nanomedicine; 2006; 1(1):105-7. PubMed ID: 17722268
[TBL] [Abstract][Full Text] [Related]
5. Comparative analysis of protein structure of common Hb Q variants.
Yadav AK
Indian J Pathol Microbiol; 2010; 53(4):696-8. PubMed ID: 21045395
[TBL] [Abstract][Full Text] [Related]
6. Hb Tak: a beta chain elongation at the end of the beta chain, in a Taiwanese.
Shih MC; Wu KH; Liu SC; Chang JG
Hemoglobin; 2005; 29(1):65-7. PubMed ID: 15768557
[TBL] [Abstract][Full Text] [Related]
7. Dominantly Inherited beta-Thalassemia.
Efremov GD
Hemoglobin; 2007; 31(2):193-207. PubMed ID: 17486503
[TBL] [Abstract][Full Text] [Related]
8. Analysis of functional aberration of some important beta hemoglobinopathies (hemoglobin C, D, E, and S) from nanostructures.
Wiwanitkit V
Nanomedicine; 2005 Sep; 1(3):213-5. PubMed ID: 17292080
[TBL] [Abstract][Full Text] [Related]
9. Hb Montfermeil [beta 130(H8) Tyr-->Cys]: suggests a key role for the interaction between helix A and H in oxygen affinity of the hemoglobin molecule.
Kister J; Baudin-Creuza V; Kiger L; Préhu C; Papassotiriou I; Riou J; Galactéros F; Wajcman H
Blood Cells Mol Dis; 2005; 34(2):166-73. PubMed ID: 15727901
[TBL] [Abstract][Full Text] [Related]
10. Identification of the Hb Lepore phenotype by HPLC.
Ropero P; González FA; Sánchez J; Anguita E; Asenjo S; Del Arco A; Murga MJ; Ramos R; Fernández C; Villegas A
Haematologica; 1999 Dec; 84(12):1081-4. PubMed ID: 10586208
[TBL] [Abstract][Full Text] [Related]
11. Hb Southampton [beta106(G8)Leu-->Pro, CTG-->CCG] in an Argentinean boy.
Eandi Eberle S; Noguera NI; Sciuccati G; Bonduel M; Díaz L; Staciuk R; Feliu-Torres A
Hemoglobin; 2006; 30(3):401-3. PubMed ID: 16840233
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Electrospray mass spectrometric characterization of hemoglobin Q (Hb Q-India) and a double mutant hemoglobin S/D in clinical samples.
Mandal AK; Bisht S; Bhat VS; Krishnaswamy PR; Balaram P
Clin Biochem; 2008 Jan; 41(1-2):75-81. PubMed ID: 17959160
[TBL] [Abstract][Full Text] [Related]
14. Unstable and thalassemic alpha chain hemoglobin variants: a cause of Hb H disease and thalassemia intermedia.
Wajcman H; Traeger-Synodinos J; Papassotiriou I; Giordano PC; Harteveld CL; Baudin-Creuza V; Old J
Hemoglobin; 2008; 32(4):327-49. PubMed ID: 18654884
[TBL] [Abstract][Full Text] [Related]
15. [Estimation of the frequency of amino acid substitutions causing instability of the spatial structure in an overall mutation spectrum of alpha- and beta-subunits of human hemoglobin].
Kolchanov NA; Shindialov IN
Genetika; 1985 Oct; 21(10):1740-8. PubMed ID: 4065561
[TBL] [Abstract][Full Text] [Related]
16. Impaired binding of AHSP to alpha chain variants: Hb Groene Hart illustrates a mechanism leading to unstable hemoglobins with alpha thalassemic like syndrome.
Vasseur-Godbillon C; Marden MC; Giordano P; Wajcman H; Baudin-Creuza V
Blood Cells Mol Dis; 2006; 37(3):173-9. PubMed ID: 17052927
[TBL] [Abstract][Full Text] [Related]
17. 3(10)-Helix adjoining alpha-helix and beta-strand: sequence and structural features and their conservation.
Pal L; Dasgupta B; Chakrabarti P
Biopolymers; 2005 Jun; 78(3):147-62. PubMed ID: 15759287
[TBL] [Abstract][Full Text] [Related]
18. Hb Marineo [beta70(E14)Ala-->Val]: a silent hemoglobin variant with a mutation within the heme pocket.
Giambona A; Vinciguerra M; Cassarà F; Li Muli R; Leto F; Passarello C; Wajcman H; Maggio A
Hemoglobin; 2006; 30(2):139-48. PubMed ID: 16798637
[TBL] [Abstract][Full Text] [Related]
19. Structure of human hemoglobin messenger RNA and its relation to hemoglobinopathies.
Wilson JT; Marotta CA; Forget BG; Weissman SM
Trans Assoc Am Physicians; 1977; 90():117-26. PubMed ID: 205979
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
