Humphries SE - Search Results

1

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

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 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

4

A study of the structure of the gene for lecithin: cholesterol acyltransferase in four unrelated individuals with familial lecithin: cholesterol acyltransferase deficiency.

Humphries SE, Chaves ME, Tata F, Lima VL, Owen JS, Borysiewicz LK, Catapano A, Vergani C, Gjone E, Clemens MR, et al. Humphries SE, et al. Clin Sci (Lond). 1988 Jan;74(1):91-6. doi: 10.1042/cs0740091. Clin Sci (Lond). 1988. PMID: 3338256

5

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

6

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

7

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

8

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

9

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

10

Familial apolipoprotein CII deficiency: a preliminary analysis of the gene defect in two independent families.

Humphries SE, Williams L, Myklebost O, Stalenhoef AF, Demacker PN, Baggio G, Crepaldi G, Galton DJ, Williamson R. Humphries SE, et al. Hum Genet. 1984;67(2):151-5. doi: 10.1007/BF00272990. Hum Genet. 1984. PMID: 6547689

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