人类血红蛋白 - Suppr

Suppr

超能文献

HUMAN HAEMOGLOBINS.

作者信息

HUEHNS E R, SHOOTER E M

出版信息

J Med Genet. 1965 Mar;2(1):48-90. doi: 10.1136/jmg.2.1.48.

DOI:10.1136/jmg.2.1.48

PMID:14296925

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1012805/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db44/1012805/b652361645db/jmedgene00330-0053-a.jpg

相似文献

HUMAN HAEMOGLOBINS.

J Med Genet. 1965 Mar;2(1):48-90. doi: 10.1136/jmg.2.1.48.

Segregation-ratio advantage of abnormal haemoglobins.

Nature. 1961 Oct 28;192:382-3. doi: 10.1038/192382a0.

HAEMOGLOBINS N AND P IN ITALIAN FAMILIES.

Nature. 1963 Nov 16;200:658-9. doi: 10.1038/200658a0.

SIMULTANEOUS OCCURRENCE OF HAEMOGLOBINS C AND LEPORE IN AN AFRO-AMERICAN.

Nature. 1964 Oct 10;204:163-6. doi: 10.1038/204163a0.

HEMOGLOBIN: A REVIEW.

J Miss State Med Assoc. 1964 Nov;5:430-3.

[Genetic factors responsible for hemoglobin synthesis in the human species].

Concours Med. 1963 Mar 9;85:1613-8.

[Contribution of studies on human hemoglobin to the solution of some basic problems of genetics].

Blut. 1962;8:449-63. doi: 10.1007/BF01631299.

COMPENSATORY EFFECTS IN THE SYNTHESIS OF HEMOGLOBIN POLYPEPTIDE CHAINS.

Cold Spring Harb Symp Quant Biol. 1964;29:357-74. doi: 10.1101/sqb.1964.029.01.038.

[THE HEMOGLOBIN M-RADOM CLINICAL SYNDROME].

Pediatr Pol. 1963 Dec;38:1043-50.

[A NEW KIND OF DREPANOCYTIC ANEMIA: HEMOGLOBIN A-HEMOGLOBIN LEPORE DISEASE].

Prog Med (Napoli). 1963 Sep 30;19:545-8.

引用本文的文献

Single-cell RNA sequencing identifies the expression of hemoglobin in chondrocyte cell subpopulations in osteoarthritis.

BMC Mol Cell Biol. 2024 Dec 30;25(1):28. doi: 10.1186/s12860-024-00519-3.

Prognostic nomogram based on the gamma-glutamyl transpeptidase-to-platelet ratio for patients with compensated cirrhotic hepatocellular carcinoma after local ablation.

Front Oncol. 2024 Jul 11;14:1406764. doi: 10.3389/fonc.2024.1406764. eCollection 2024.

In vitro blood sample assessment: investigating correlation of laboratory hemoglobin and spectral properties of dual-energy CT measurements (ρ/Z).

Eur Radiol. 2024 Dec;34(12):7934-7943. doi: 10.1007/s00330-024-10820-6. Epub 2024 Jun 10.

A systems pharmacology model for gene therapy in sickle cell disease.

CPT Pharmacometrics Syst Pharmacol. 2021 Jul;10(7):696-708. doi: 10.1002/psp4.12638. Epub 2021 Jun 17.

Expressed sequence tags for bovine muscle satellite cells, myotube formed-cells and adipocyte-like cells.

PLoS One. 2013 Nov 5;8(11):e79780. doi: 10.1371/journal.pone.0079780. eCollection 2013.

Intrinsic regulation of hemoglobin expression by variable subunit interface strengths.

FEBS J. 2012 Feb;279(3):361-9. doi: 10.1111/j.1742-4658.2011.08437.x. Epub 2011 Dec 22.

Developmental expression of human hemoglobins mediated by maturation of their subunit interfaces.

Protein Sci. 2010 Aug;19(8):1595-9. doi: 10.1002/pro.441.

Energetic differences at the subunit interfaces of normal human hemoglobins correlate with their developmental profile.

Biochemistry. 2009 Aug 18;48(32):7568-74. doi: 10.1021/bi900857r.

Human embryonic, fetal, and adult hemoglobins have different subunit interface strengths. Correlation with lifespan in the red cell.

Protein Sci. 2007 Aug;16(8):1641-58. doi: 10.1110/ps.072891007.

Genetic variation in red-cell adenosine deaminase and glucosephosphate isomerase in a laboratory colony of the marsupial Sminthopsis crassicaudata (Gould).

Biochem Genet. 1984 Apr;22(3-4):221-9. doi: 10.1007/BF00484226.

本文引用的文献

Increase in Haemoglobin A(2) Appearing After Homograft of Foetal Haemopoietic Tissue.

Br Med J. 1961 May 13;1(5236):1349-52. doi: 10.1136/bmj.1.5236.1349.

The Inheritance of Sickle Cell Anemia.

Science. 1949 Jul 15;110(2846):64-6. doi: 10.1126/science.110.2846.64.

FORMATION OF THE PEPTIDE CHAIN OF HEMOGLOBIN.

Proc Natl Acad Sci U S A. 1960 Aug;46(8):1030-8. doi: 10.1073/pnas.46.8.1030.

ON DISSOCIATION AND RECOMBINATION OF HUMAN ADULT HEMOGLOBINS A, S, AND C.

Proc Natl Acad Sci U S A. 1958 Jun;44(6):522-9. doi: 10.1073/pnas.44.6.522.

Sickle cell anemia a molecular disease.

Science. 1949 Nov 25;110(2865):543-8. doi: 10.1126/science.110.2865.543.

Effect of oxygen tension and of pH on the sickling and mechanical fragility of erythrocytes from patients with sickle cell anemia and the sickle cell trait.

J Lab Clin Med. 1951 May;37(5):789-802.

Studies on abnormal hemoglobins. I. Their demonstration in sickle cell anemia and other hematologic disorders by means of alkali denaturation.

Blood. 1951 May;6(5):413-28.

A human hemoglobin with lowered oxygen affinity and impaired heme-heme interactions.

J Clin Invest. 1961 Oct;40(10):1826-33. doi: 10.1172/JCI104406.

An abnormal human foetal haemoglobin with an abnormal alpha-polypeptide chain.

Nature. 1962 May 26;194:743-5. doi: 10.1038/194743a0.

Controller genes in synthesis of human haemoglobin.

Nature. 1962 May 12;194:607-9. doi: 10.1038/194607b0.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验