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Items: 1 to 20 of 1888

1.

IVS-II-648/649 (-T) (HBB: c.316-202del) Triggers a Novel β-Thalassemia Phenotype.

Azimi A, Alibakhshi R, Hayati H, Tahmasebi S, Alimoradi S.

Hemoglobin. 2017 Jan;41(1):44-46. doi: 10.1080/03630269.2017.1308376. Epub 2017 May 5.

PMID:
28475449
2.

Presence of the IVS-I-6-Mutated Allele in Beta-Thalassemia Major Patients Correlates with Extramedullary Hematopoiesis Incidence.

Sousos N, Adamidou D, Klonizakis P, Agapidou A, Theodoridou S, Spanos G, Psarras K, Vetsiou E, Vyzantiadis TA, Vlachaki E.

Acta Haematol. 2017;137(3):175-182. doi: 10.1159/000463919. Epub 2017 Apr 12.

PMID:
28399542
3.

Combination of Hb Heze [β144(HC1)Lys→Arg; HBB: c.434A>G] and β0-Thalassemia in a Chinese Patient with β-Thalassemia Intermedia.

Li Y, Yan JM, Zhou JY, Lu YC, Li DZ.

Hemoglobin. 2017 Jan;41(1):47-49. doi: 10.1080/03630269.2017.1290652. Epub 2017 Apr 3.

PMID:
28366026
4.

Interrelationship among Fe-His Bond Strengths, Oxygen Affinities, and Intersubunit Hydrogen Bonding Changes upon Ligand Binding in the β Subunit of Human Hemoglobin: The Alkaline Bohr Effect.

Nagatomo S, Okumura M, Saito K, Ogura T, Kitagawa T, Nagai M.

Biochemistry. 2017 Mar 7;56(9):1261-1273. doi: 10.1021/acs.biochem.6b01118. Epub 2017 Feb 24.

PMID:
28199095
5.

Cross-Sectional Study for the Detection of Mutations in the Beta-Globin Gene Among Patients with Hemoglobinopathies in the Bengali Population.

Panja A, Chowdhury P, Chakraborty S, Ghosh TK, Basu A.

Genet Test Mol Biomarkers. 2017 Jan;21(1):39-45. doi: 10.1089/gtmb.2016.0186. Epub 2016 Nov 9.

PMID:
27828729
6.

The Beta Subunit of Hemoglobin (HBB2/HBB) Suppresses Neuroblastoma Growth and Metastasis.

Maman S, Sagi-Assif O, Yuan W, Ginat R, Meshel T, Zubrilov I, Keisari Y, Lu W, Lu W, Witz IP.

Cancer Res. 2017 Jan 1;77(1):14-26. doi: 10.1158/0008-5472.CAN-15-2929. Epub 2016 Oct 28.

PMID:
27793844
7.

Intracranial Aneurysms in Sickle-Cell Disease Are Associated With the Hemoglobin SS Genotype But Not With Moyamoya Syndrome.

Birkeland P, Gardner K, Kesse-Adu R, Davies J, Lauritsen J, Rom Poulsen F, Tolias CM, Thein SL.

Stroke. 2016 Jul;47(7):1710-3. doi: 10.1161/STROKEAHA.116.012664. Epub 2016 Jun 14.

8.

The molecular characterization of Beta globin gene in thalassemia patients reveals rare and a novel mutations in Pakistani population.

Yasmeen H, Toma S, Killeen N, Hasnain S, Foroni L.

Eur J Med Genet. 2016 Aug;59(8):355-62. doi: 10.1016/j.ejmg.2016.05.016. Epub 2016 Jun 1.

PMID:
27263053
9.

Sickle cell disease in India: A perspective.

Serjeant GR, Ghosh K, Patel J.

Indian J Med Res. 2016 Jan;143(1):21-4. doi: 10.4103/0971-5916.178582. No abstract available.

10.

Detection of β-Thalassemia Mutations Using TaqMan Single Nucleotide Polymorphism Genotyping Assays.

Alwazani WA, Zahid R, Elaimi A, Bajouh O, Hindawi S, Arab B, Damanhouri G, Saka MY, Turki R, Khan JA, Dallol A, Abuzenadah AM.

Genet Test Mol Biomarkers. 2016 Mar;20(3):154-7. doi: 10.1089/gtmb.2015.0222. Epub 2016 Feb 18.

PMID:
26890443
11.

The Codon 35 (A > G) (HBB: c.107A > G) at the α-β Chain Interface of the β-Globin Gene: A Silent Mutation?

Wu MY, Li DZ.

Hemoglobin. 2016;40(1):56-8. doi: 10.3109/03630269.2015.1099547. Epub 2015 Nov 2.

PMID:
26754300
12.

First Detection of the -27 (A > G) (HBB: c.-77A > G) Mutation of the β-Globin Gene in a Chinese Family.

Wu MY, Li DZ.

Hemoglobin. 2016;40(1):59-60. doi: 10.3109/03630269.2015.1100118. Epub 2015 Nov 10.

PMID:
26554738
13.

Characterization of the HBB: c.*233G > C Variant: No Evidence of a β-Thalassemic Phenotype.

Smith DL, Mitui M, Park JY, Luu HS, Timmons CF.

Hemoglobin. 2016;40(1):25-8. doi: 10.3109/03630269.2015.1101002. Epub 2015 Nov 2.

PMID:
26524961
14.

Quantitative trait locus analysis of parasite density reveals that HbS gene carriage protects severe malaria patients against Plasmodium falciparum hyperparasitaemia.

do Sambo MR, Penha-Gonçalves C, Trovoada MJ, Costa J, Lardoeyt R, Coutinho A.

Malar J. 2015 Oct 7;14:393. doi: 10.1186/s12936-015-0920-z.

15.

The Spectrum of β-Thalassemia Mutations in a Population from the Brazilian Amazon.

Silva AN, Cardoso GL, Cunha DA, Diniz IG, Santos SE, Andrade GB, Trindade SM, Cardoso Mdo S, Francês LT, Guerreiro JF.

Hemoglobin. 2016;40(1):20-4. doi: 10.3109/03630269.2015.1083443. Epub 2015 Sep 15.

PMID:
26372288
16.

Prevalence of hemoglobin E in Yunnan Province of Southwest China.

He J, Zeng X, Zhang Y, Su J, Ding X, Li S, Xu Y, Pu J, Jin C, Zhu B.

Hematology. 2016 Jan;21(1):54-9. doi: 10.1179/1607845415Y.0000000044. Epub 2015 Aug 20.

PMID:
26292035
18.

XmnI POLYMORPHISM AND DISEASE SEVERITY IN PATIENTS WITH BETA THALASSEMIA FROM NORTHERN PAKISTAN.

Hanif TB, Ahmed S, Anwar J, Kazmi SK.

J Ayub Med Coll Abbottabad. 2015 Jan-Mar;27(1):13-6.

PMID:
26182728
19.

Generation and Characterization of a Transgenic Mouse Carrying a Functional Human β -Globin Gene with the IVSI-6 Thalassemia Mutation.

Breveglieri G, Mancini I, Bianchi N, Lampronti I, Salvatori F, Fabbri E, Zuccato C, Cosenza LC, Montagner G, Borgatti M, Altruda F, Fagoonee S, Carandina G, Rubini M, Aiello V, Breda L, Rivella S, Gambari R, Finotti A.

Biomed Res Int. 2015;2015:687635. doi: 10.1155/2015/687635. Epub 2015 May 4.

20.

Why the DNA self-depurination mechanism operates in HB-β but not in β-globin paralogs HB-δ, HB-ɛ1, HB-γ1 and HB-γ2.

Amosova O, Alvarez-Dominguez JR, Fresco JR.

Mutat Res. 2015 Aug;778:11-7. doi: 10.1016/j.mrfmmm.2015.05.001. Epub 2015 May 19.

PMID:
26042536

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