[人类血红蛋白研究对解决遗传学一些基本问题的贡献] - Suppr

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

作者信息

VOGEL F

出版信息

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

DOI:10.1007/BF01631299

PMID:13997622

Abstract

摘要

相似文献

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

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

A SURVEY OF CORD BLOODS FOR ABNORMAL HEMOGLOBIN, WITH FURTHER OBSERVATIONS ON HEMOGLOBIN. I. BURLINGTON.

Am J Obstet Gynecol. 1964 Mar 15;88:816-22. doi: 10.1016/0002-9378(64)90617-9.

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

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

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.

[A CASE OF MICRODREPANOCYTIC DISEASE DUE TO S HEMOGLOBIN AND A VARIETY OF MICROCYTHEMIA WITH NORMAL QUOTA OF A2 HEMOGLOBIN AND ELEVATED QUOTA OF F HEMOGLOBIN (THIRD VARIETY OF MICRODREPANOCYTIC DISEASE)].

Prog Med (Napoli). 1964 Aug 15;20:509-13.

HUMAN HAEMOGLOBINS.

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

[STUDY OF 3 FAMILIES WITH HEMOGLOBIN D DISEASE].

Haematologica. 1963;48:873-84.

The clinical implications of hemoglobin structure.

Pediatrics. 1963 May;31:780-5.

本文引用的文献

An unstable intermediate carrying information from genes to ribosomes for protein synthesis.

Nature. 1961 May 13;190:576-581. doi: 10.1038/190576a0.

THE BAR "GENE" A DUPLICATION.

Science. 1936 Feb 28;83(2148):210-1. doi: 10.1126/science.83.2148.210.

AN RNA-PROTEIN CODE BASED ON REPLACEMENT DATA.

Proc Natl Acad Sci U S A. 1962 Mar;48(3):461-71. doi: 10.1073/pnas.48.3.461.

GENETIC CONTROL OF THE alpha- AND beta-CHAINS OF HEMOGLOBIN.

Proc Natl Acad Sci U S A. 1960 Nov;46(11):1492-501. doi: 10.1073/pnas.46.11.1492.

A COMPARISON OF ANIMAL HEMOGLOBINS BY TRYPTIC PEPTIDE PATTERN ANALYSIS.

Proc Natl Acad Sci U S A. 1960 Oct;46(10):1349-60. doi: 10.1073/pnas.46.10.1349.

ON THE IMPOSSIBILITY OF ALL OVERLAPPING TRIPLET CODES IN INFORMATION TRANSFER FROM NUCLEIC ACID TO PROTEINS.

Proc Natl Acad Sci U S A. 1957 Aug 15;43(8):687-94. doi: 10.1073/pnas.43.8.687.

Close Linkage between Mutations with Similar Effects.

Proc Natl Acad Sci U S A. 1942 May;28(5):205-10. doi: 10.1073/pnas.28.5.205.

Sickle cell anemia a molecular disease.

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

Pseudoallelism and gene evolution.

Cold Spring Harb Symp Quant Biol. 1951;16:159-74. doi: 10.1101/sqb.1951.016.01.014.

Genetic aspects of sickle cell anemia and microdrepanocytic disease.

Blood. 1952 Apr;7(4):429-35.

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

作者信息

VOGEL F

出版信息

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

DOI:10.1007/BF01631299

PMID:13997622

Abstract

摘要

相似文献

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

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

A SURVEY OF CORD BLOODS FOR ABNORMAL HEMOGLOBIN, WITH FURTHER OBSERVATIONS ON HEMOGLOBIN. I. BURLINGTON.

Am J Obstet Gynecol. 1964 Mar 15;88:816-22. doi: 10.1016/0002-9378(64)90617-9.

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

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

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.

Prog Med (Napoli). 1964 Aug 15;20:509-13.

HUMAN HAEMOGLOBINS.

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

[STUDY OF 3 FAMILIES WITH HEMOGLOBIN D DISEASE].

Haematologica. 1963;48:873-84.

The clinical implications of hemoglobin structure.

Pediatrics. 1963 May;31:780-5.

本文引用的文献

An unstable intermediate carrying information from genes to ribosomes for protein synthesis.

Nature. 1961 May 13;190:576-581. doi: 10.1038/190576a0.

THE BAR "GENE" A DUPLICATION.

Science. 1936 Feb 28;83(2148):210-1. doi: 10.1126/science.83.2148.210.

AN RNA-PROTEIN CODE BASED ON REPLACEMENT DATA.

Proc Natl Acad Sci U S A. 1962 Mar;48(3):461-71. doi: 10.1073/pnas.48.3.461.

GENETIC CONTROL OF THE alpha- AND beta-CHAINS OF HEMOGLOBIN.

Proc Natl Acad Sci U S A. 1960 Nov;46(11):1492-501. doi: 10.1073/pnas.46.11.1492.

A COMPARISON OF ANIMAL HEMOGLOBINS BY TRYPTIC PEPTIDE PATTERN ANALYSIS.

Proc Natl Acad Sci U S A. 1960 Oct;46(10):1349-60. doi: 10.1073/pnas.46.10.1349.

ON THE IMPOSSIBILITY OF ALL OVERLAPPING TRIPLET CODES IN INFORMATION TRANSFER FROM NUCLEIC ACID TO PROTEINS.

Proc Natl Acad Sci U S A. 1957 Aug 15;43(8):687-94. doi: 10.1073/pnas.43.8.687.

Close Linkage between Mutations with Similar Effects.

Proc Natl Acad Sci U S A. 1942 May;28(5):205-10. doi: 10.1073/pnas.28.5.205.

Sickle cell anemia a molecular disease.

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

Pseudoallelism and gene evolution.

Cold Spring Harb Symp Quant Biol. 1951;16:159-74. doi: 10.1101/sqb.1951.016.01.014.

Genetic aspects of sickle cell anemia and microdrepanocytic disease.

Blood. 1952 Apr;7(4):429-35.