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Literature DB >> 6360557

Report of the Committee on the Genetic Constitution of Chromosomes 18, 19, 20, 21, and 22.

A Westerveld, S Naylor.

Abstract

Mesh：

Year: 1984 PMID： 6360557 DOI： 10.1159/000132008

Source DB: PubMed Journal: Cytogenet Cell Genet ISSN： 0301-0171

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11 in total

1. Four restriction fragment length polymorphisms revealed by probes from a single cosmid map to chromosome 19.

Authors: L Bufton; G A Bruns; R E Magenis; D Tomar; D Shaw; D Brook; M Litt
Journal: Am J Hum Genet Date: 1986-04 Impact factor: 11.025

2. Abnormal blood rheology and chronic low grade inflammation: possible risk factors for accelerated atherosclerosis and coronary artery disease in Lewis negative subjects.

Authors: Tamas Alexy; Eszter Pais; Rosalinda B Wenby; Wendy J Mack; Howard N Hodis; Naoko Kono; Jun Wang; Oguz K Baskurt; Timothy C Fisher; Herbert J Meiselman
Journal: Atherosclerosis Date: 2015-01-21 Impact factor: 5.162

3. Molecular cloning of a novel splice variant of human type IVA (PDE-IVA) cyclic AMP phosphodiesterase and localization of the gene to the p13.2-q12 region of human chromosome 19 [corrected].

Authors: Y M Horton; M Sullivan; M D Houslay
Journal: Biochem J Date: 1995-06-01 Impact factor: 3.857

4. Localisation of genetic markers and orientation of the linkage group on chromosome 19.

Authors: J D Brook; D J Shaw; L Meredith; G A Bruns; P S Harper
Journal: Hum Genet Date: 1984 Impact factor: 4.132

5. Isolation and characterisation of a cDNA clone for human apolipoprotein CI and assignment of the gene to chromosome 19.

Authors: F Tata; I Henry; A F Markham; S C Wallis; D Weil; K H Grzeschik; C Junien; R Williamson; S E Humphries
Journal: Hum Genet Date: 1985 Impact factor: 4.132

6. Isolation and sequence of a human apolipoprotein CII cDNA clone and its use to isolate and map to human chromosome 19 the gene for apolipoprotein CII.

Authors: C L Jackson; G A Bruns; J L Breslow
Journal: Proc Natl Acad Sci U S A Date: 1984-05 Impact factor: 11.205

Report of the Committee on the Genetic Constitution of Chromosomes 18, 19, 20, 21, and 22.

1. Four restriction fragment length polymorphisms revealed by probes from a single cosmid map to chromosome 19.

2. Abnormal blood rheology and chronic low grade inflammation: possible risk factors for accelerated atherosclerosis and coronary artery disease in Lewis negative subjects.

3. Molecular cloning of a novel splice variant of human type IVA (PDE-IVA) cyclic AMP phosphodiesterase and localization of the gene to the p13.2-q12 region of human chromosome 19 [corrected].

4. Localisation of genetic markers and orientation of the linkage group on chromosome 19.

5. Isolation and characterisation of a cDNA clone for human apolipoprotein CI and assignment of the gene to chromosome 19.

6. Isolation and sequence of a human apolipoprotein CII cDNA clone and its use to isolate and map to human chromosome 19 the gene for apolipoprotein CII.

7. The human myoglobin gene: a third dispersed globin locus in the human genome.

8. Linkage relationships of the gene for apolipoprotein CII with loci on chromosome 19.

9. The locus for apolipoprotein E (apoE) is close to the Lutheran (Lu) blood group locus on chromosome 19.

10. The apolipoprotein CII gene: subchromosomal localisation and linkage to the myotonic dystrophy locus.