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.
97 related articles for article (PubMed ID: 10569724)
1. Hb Bologna-St. Orsola [beta146(HC3)His-->Tyr]: a new high oxygen affinity variant with halved Bohr effect and highly reduced reactivity towards 2,3-diphosphoglycerate. Ivaldi G; David O; Paradossi V; Baffico M; Scimè Degani V; Leone D; Baldi M; Parodi MI; Bernardi P; Ricco G Hemoglobin; 1999 Nov; 23(4):353-9. PubMed ID: 10569724 [No Abstract] [Full Text] [Related]
2. A second case of Hb Bologna-St. Orsola [beta146(HC3)His-->Tyr] in an unrelated family of Anglo-Celtic origin. Gilbert AT; Fleming PJ; Hertzberg MS Hemoglobin; 2000 May; 24(2):139-42. PubMed ID: 10870885 [No Abstract] [Full Text] [Related]
6. A case of hemoglobin Hiroshima (β146 histidine to aspartic acid) with compensatory erythremia and undetectable HbA₁c. Nishimori H; Harano K; Wada H; Takano S; Fukuda S; Takehara Y; Matsumoto H; Kumagai I; Tanimoto M; Takeda S Int J Hematol; 2012 Jun; 95(6):697-701. PubMed ID: 22484594 [TBL] [Abstract][Full Text] [Related]
7. Hb Fukuoka [beta 2(NA2)His----Tyr]: a new mutation at the 2,3-diphosphoglycerate binding site. Harano T; Harano K; Ueda S; Imai K; Ohkuma A; Koya Y; Takahashi H Hemoglobin; 1990; 14(2):199-205. PubMed ID: 2272842 [No Abstract] [Full Text] [Related]
8. Effects of substitutions of lysine and aspartic acid for asparagine at beta 108 and of tryptophan for valine at alpha 96 on the structural and functional properties of human normal adult hemoglobin: roles of alpha 1 beta 1 and alpha 1 beta 2 subunit interfaces in the cooperative oxygenation process. Tsai CH; Shen TJ; Ho NT; Ho C Biochemistry; 1999 Jul; 38(27):8751-61. PubMed ID: 10393550 [TBL] [Abstract][Full Text] [Related]
9. Assessment of roles of surface histidyl residues in the molecular basis of the Bohr effect and of beta 143 histidine in the binding of 2,3-bisphosphoglycerate in human normal adult hemoglobin. Fang TY; Zou M; Simplaceanu V; Ho NT; Ho C Biochemistry; 1999 Oct; 38(40):13423-32. PubMed ID: 10529219 [TBL] [Abstract][Full Text] [Related]
10. Hb Toulon [alpha77(EF6)Pro-->His]: a new variant due to a mutation in the alpha2 gene found during measurement of glycated hemoglobin. Badens C; Léna-Russo D; Lacan P; Francina A; Promé D; Riou J; Geoffroy M; Ayavou T; Kister J; Galactéros F; Wajcman H Hemoglobin; 1999 Nov; 23(4):367-71. PubMed ID: 10569726 [No Abstract] [Full Text] [Related]
11. Hemoglobinopathy York [beta146 (HC3) His==>Pro]: first report of a family history. Misgeld E; Gattermann N; Wehmeier A; Weiland C; Peters U; Kohne E Ann Hematol; 2001 Jun; 80(6):365-7. PubMed ID: 11475152 [TBL] [Abstract][Full Text] [Related]
12. Two new alpha chain variants: Hb Boghé [alpha58(E7)His-->Gln, alpha2], a variant on the distal histidine, and Hb CHarolles [alpha103(G10)His-Tyr, alpha1]. Lacan P; Francina A; Souillet G; Aubry M; Couprie N; Dementhon L; Becchi M Hemoglobin; 1999 Nov; 23(4):345-52. PubMed ID: 10569723 [TBL] [Abstract][Full Text] [Related]
13. A new beta chain variant, Hb Vienna or beta77(EF1)His-->Gln. Hopmeier P; Plaseska-Karanfilska D; Efremov GD Hemoglobin; 1998 Jul; 22(4):391-5. PubMed ID: 9730371 [No Abstract] [Full Text] [Related]
14. Haemoglobin Hallamshire (beta146 HIS --> TYR): a new high oxygen affinity haemoglobin responsible for familial erythrocytosis. Leach M; Greaves M; Porter N; Williamson D; Brown K Clin Lab Haematol; 1996 Dec; 18(4):237-9. PubMed ID: 9054694 [TBL] [Abstract][Full Text] [Related]
15. Hemoglobin Rouen (alpha-140 (HC2) Tyr-->His): alteration of the alpha-chain C-terminal region and moderate increase in oxygen affinity. Wajcman H; Kister J; Marden M; Lahary A; Monconduit M; Galacteros F Biochim Biophys Acta; 1992 Oct; 1180(1):53-7. PubMed ID: 1390944 [TBL] [Abstract][Full Text] [Related]
16. A mutagenic study of the allosteric linkage of His(HC3)146 beta in haemoglobin. Shih DT; Luisi BF; Miyazaki G; Perutz MF; Nagai K J Mol Biol; 1993 Apr; 230(4):1291-6. PubMed ID: 8487305 [TBL] [Abstract][Full Text] [Related]
17. Hemoglobin Okayama [beta 2 (NA 2) His replaced by Gln]: a new 'silent' hemoglobin variant with substituted amino acid residue at the 2,3-diphosphoglycerate binding site. Harano T; Harano K; Shibata S; Ueda S; Mori H; Arimasa N FEBS Lett; 1983 May; 156(1):20-2. PubMed ID: 6852251 [TBL] [Abstract][Full Text] [Related]