Pascal and Francis Bibliographic Databases

Help

Search results

Your search

au.\*:("COETZEE, G. A")

Publication Year[py]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Discipline (document) [di]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Author Country

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Results 1 to 25 of 52

  • Page / 3
Export

Selection :

  • and

Degradation of receptors and their ligandsVAN DER WESTHUYZEN, D. R; COETZEE, G. A.Research monographs in cell and tissue physiology. 1985, Vol 11, pp 91-111, issn 0378-6129Article

Polymorphic exonic CAG micro satellites in the gene amplified in breast cancer (AIB1 gene)SHIRAZI, S. K; BOBER, M. A; COETZEE, G. A et al.Clinical genetics. 1998, Vol 54, Num 1, pp 102-103, issn 0009-9163Article

Androgen metabolism and prostate cancer : Establishing a model of genetic susceptibilityROSS, R. K; PIKE, M. C; COETZEE, G. A et al.Cancer research (Baltimore). 1998, Vol 58, Num 20, pp 4497-4504, issn 0008-5472Article

A polymorphism in intron 6 of the CYP17 geneCROCITTO, L. E; FEIGELSON, H. S; YU, M. C et al.Clinical genetics. 1997, Vol 52, Num 1, pp 68-69, issn 0009-9163Article

The apolipoprotein E2 (Arg145Cys) mutation causes autosomal dominant type III hyperlipoproteinemia with incomplete penetranceDE VILLIERS, W. J. S; VAN DER WESTHUYZEN, D. R; COETZEE, G. A et al.Arteriosclerosis, thrombosis, and vascular biology. 1997, Vol 17, Num 5, pp 865-872, issn 1079-5642Article

The CAG and GGC microsatellites of the androgen receptor gene are in linkage disequilibrium in men with prostate cancerIRVINE, R. A; YU, M. C; ROSS, R. K et al.Cancer research (Baltimore). 1995, Vol 55, Num 9, pp 1937-1940, issn 0008-5472Article

Cytochrome P450C17α gene (CYP17) polymorphism is associated with serum estrogen and progesterone concentrationsFEIGELSON, H. S; SHAMES, L. S; PIKE, M. C et al.Cancer research (Baltimore). 1998, Vol 58, Num 4, pp 585-587, issn 0008-5472Article

A missense mutation in the low density lipoprotein receptor gene causes familial hypercholesterolemia in Sephardic JewsLEITERSDORF, E; RESHEF, A; MEINER, V et al.Human genetics. 1993, Vol 91, Num 2, pp 141-147, issn 0340-6717Article

Identification of two new LDL-receptor mutations causing homozygous familial hypercholesterolemia in a South African of Indian originRUBINSZTEIN, D. C; ISHWARLAL JIALAL; LEITERSDORF, E et al.Biochimica et biophysica acta. Molecular basis of disease. 1993, Vol 1182, Num 1, pp 75-82, issn 0925-4439Article

Low density lipoprotein receptor founder mutations in Afrikaner familial hypercholesterolaemic patients : a comparison of two geographical areasVAN ROGGEN, F. G; VAN DER WESTHUYZEN, D. R; MARAIS, A. D et al.Human genetics. 1991, Vol 88, Num 2, pp 204-208, issn 0340-6717Article

Sex steroid hormones and genetic susceptibility to breast and prostate cancerFEIGELSON, H. S; ROSS, R. K; YU, M. C et al.Drug metabolism reviews (Softcover ed.). 1998, Vol 30, Num 2, pp 421-434, issn 0360-2532Conference Paper

Familial defective apolipoprotein-B is rare in hypercholesterolaemic South African Afrikaners, coloureds and IndiansRUBINSZTEIN, D. C; COETZEE, G. A; VAN DER WESTHUYZEN, D. R et al.SAMJ. South African medical journal. 1995, Vol 85, Num 5, pp 355-357, issn 0256-9574Article

Characterization of six patients who are double heterozygotes for familial hypercholesterolemia and familial defective apo B-100RUBINSZTEIN, D. C; RAAL, F. J; SEFTEL, H. C et al.Arteriosclerosis and thrombosis. 1993, Vol 13, Num 7, pp 1076-1081, issn 1049-8834Article

A common lithuanian mutation causing familial hypercholesterolemia in Ashkenazi jewsMEINER, V; LANDSBERGER, D; BERKMAN, N et al.American journal of human genetics. 1991, Vol 49, Num 2, pp 443-449, issn 0002-9297Article

Human serum amyloid A protein: the assignment of the six major isoforms to three published gene sequences and evidence for two genetic lociSTRACHAN, A. F; BRANDT, W. F; WOO, P et al.The Journal of biological chemistry (Print). 1989, Vol 264, Num 31, pp 18368-18373, issn 0021-9258Article

Deletion in the first cysteine-rich repeat of low density lipoprotein receptor impairs its transport but not lipoprotein binding in fibroblasts from a subject with familial hypercholesterolemiaLEITERSDORF, E; HOBBS, H. H; FOURIE, A. M et al.Proceedings of the National Academy of Sciences of the United States of America. 1988, Vol 85, Num 21, pp 7912-7916, issn 0027-8424Article

Two mutant low-density-lipoprotein receptors in Afrikaners slowly processed to surface forms exhibiting rapid degradation of functional heterogeneityFOURIE, A. M; COETZEE, G. A; GEVERS, W et al.Biochemical journal (London. 1906). 1988, Vol 255, Num 2, pp 411-415, issn 0006-2936Article

Low-density lipoprotein receptor deficiency resulting in familial hypercholesterolaemia in a black manCOETZEE, G. A; VAN WINGERDEN, J. J; VAN DER WESTHUYZEN, D. R et al.SAMJ. South African medical journal. 1985, Vol 67, Num 7, pp 259-261, issn 0256-9574Article

Inhibition of p160-mediated coactivation with increasing androgen receptor polyglutamine lengthIRVINE, R. A; HAN MA; YU, M. C et al.Human molecular genetics (Print). 2000, Vol 9, Num 2, pp 267-274, issn 0964-6906Article

Isothiocyanates, glutathione S-transferase M1 and T1 polymorphisms, and lung-cancer risk : a prospective study of men in Shanghai, ChinaLONDON, S. J; YUAN, J.-M; CHUNG, F.-L et al.Lancet (British edition). 2000, Vol 356, Num 9231, pp 724-729, issn 0140-6736Article

Cytochrome P450C17α gene (CYP17) polymorphism predicts use of hormone replacement therapyFEIGELSON, H. S; MCKEAN-COWDIN, R; PIKE, M. C et al.Cancer research (Baltimore). 1999, Vol 59, Num 16, pp 3908-3910, issn 0008-5472Article

A polymorphism in the CYP17 gene increases the risk of breast cancerFEIGELSON, H. S; COETZEE, G. A; KOLONEL, L. N et al.Cancer research (Baltimore). 1997, Vol 57, Num 6, pp 1063-1065, issn 0008-5472Article

FH Afrikaner-3 LDL receptor mutation results in defective LDL receptors and causes a mild form of familial hypercholesterolemiaGRAADT VAN ROGGEN, J. F; VAN DER WESTHUYZEN, D. R; COETZEE, G. A et al.Arteriosclerosis, thrombosis, and vascular biology. 1995, Vol 15, Num 6, pp 765-772, issn 1079-5642Article

Does the racial-ethnic variation in prostate cancer risk have a hormonal basis ?ROSS, R. K; COETZEE, G. A; REICHARDT, J et al.Cancer. 1995, Vol 75, Num 7, pp 1778-1782, issn 0008-543X, SUPConference Paper

Identification and properties of the proline664-leucine mutant LDL receptor in South Africans of Indian originRUBINSZTEIN, D. C; COETZEE, G. A; MARAIS, A. D et al.Journal of lipid research. 1992, Vol 33, Num 11, pp 1647-1655, issn 0022-2275Article

  • Page / 3