Humphries SE - Search Results

1

The isolation, characterisation, and chromosomal assignment of the gene for human 3-hydroxy-3-methylglutaryl coenzyme A reductase, (HMG-CoA reductase).

Humphries SE, Tata F, Henry I, Barichard F, Holm M, Junien C, Williamson R. Humphries SE, et al. Hum Genet. 1985;71(3):254-8. doi: 10.1007/BF00284585. Hum Genet. 1985. PMID: 2998972

2

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

Tata F, Henry I, Markham AF, Wallis SC, Weil D, Grzeschik KH, Junien C, Williamson R, Humphries SE. Tata F, et al. Among authors: humphries se. Hum Genet. 1985;69(4):345-9. doi: 10.1007/BF00291654. Hum Genet. 1985. PMID: 2985493

3

The structural gene for lecithin:cholesterol acyl transferase (LCAT) maps to 16q22.

Azoulay M, Henry I, Tata F, Weil D, Grzeschik KH, Chaves ME, McIntyre N, Williamson R, Humphries SE, Junien C. Azoulay M, et al. Among authors: humphries se. Ann Hum Genet. 1987 May;51(2):129-36. doi: 10.1111/j.1469-1809.1987.tb01054.x. Ann Hum Genet. 1987. PMID: 3674753

4

Identification of a deletion in the low density lipoprotein (LDL) receptor gene in a patient with familial hypercholesterolaemia.

Horsthemke B, Kessling AM, Seed M, Wynn V, Williamson R, Humphries SE. Horsthemke B, et al. Among authors: humphries se. Hum Genet. 1985;71(1):75-8. doi: 10.1007/BF00295672. Hum Genet. 1985. PMID: 2993159

5

The isolation of a genomic clone containing the apolipoprotein CII gene and the detection of linkage disequilibrium between two common DNA polymorphisms around the gene.

Wallis SC, Donald JA, Forrest LA, Williamson R, Humphries SE. Wallis SC, et al. Among authors: humphries se. Hum Genet. 1984;68(4):286-9. doi: 10.1007/BF00292585. Hum Genet. 1984. PMID: 6096256

6

The identification of a DNA polymorphism of the alpha fibrinogen gene, and the regional assignment of the human fibrinogen genes to 4q26-qter.

Humphries SE, Imam AM, Robbins TP, Cook M, Carritt B, Ingle C, Williamson R. Humphries SE, et al. Hum Genet. 1984;68(2):148-53. doi: 10.1007/BF00279305. Hum Genet. 1984. PMID: 6500566

7

Gene for apolipoprotein CII is on human chromosome 19.

Jeanpierre M, Weil D, Hors-Cayla MC, Williamson R, Junien C, Humphries SE. Jeanpierre M, et al. Among authors: humphries se. Somat Cell Mol Genet. 1984 Nov;10(6):645-9. doi: 10.1007/BF01535231. Somat Cell Mol Genet. 1984. PMID: 6594769

8

The isolation and characterisation of cDNA and genomic clones for human lecithin: cholesterol acyltransferase.

Tata F, Chaves ME, Markham AF, Scrace GD, Waterfield MD, McIntyre N, Williamson R, Humphries SE. Tata F, et al. Among authors: humphries se. Biochim Biophys Acta. 1987 Nov 20;910(2):142-8. doi: 10.1016/0167-4781(87)90066-2. Biochim Biophys Acta. 1987. PMID: 2823898

9

The gene for apolipoprotein C-II is closely linked to the gene for apolipo-protein E on chromosome 19.

Humphries SE, Berg K, Gill L, Cumming AM, Robertson FW, Stalenhoef AF, Williamson R, Børresen AL. Humphries SE, et al. Clin Genet. 1984 Nov;26(5):389-96. Clin Genet. 1984. PMID: 6094053

10

There are approximately 20 actin gene in the human genome.

Humphries SE, Whittall R, Minty A, Buckingham M, Williamson R. Humphries SE, et al. Nucleic Acids Res. 1981 Oct 10;9(19):4895-908. doi: 10.1093/nar/9.19.4895. Nucleic Acids Res. 1981. PMID: 6273789 Free PMC article.

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