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Epoxy Nanocomposites Based on the Synthetic α-Zirconium Phosphate Layer Structure

Chemistry of materials, 2004-01, Vol.16 (2), p.242-249

2004

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Relationship between the GSTM1 genetic polymorphism and susceptibility to bladder, breast and colon cancer

Carcinogenesis (New York), 1993-09, Vol.14 (9), p.1821-1824

1993

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Plectin deficiency results in muscular dystrophy with epidermolysis bullosa

Nature genetics, 1996-08, Vol.13 (4), p.450-457

1996

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Multifactorial Analysis of Differences Between Sporadic Breast Cancers and Cancers Involving BRCA1 and BRCA2 Mutations

JNCI : Journal of the National Cancer Institute, 1998-08, Vol.90 (15), p.1138-1145

1998

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Single nucleotide polymorphisms as tools in human genetics

Human molecular genetics, 2000-10, Vol.9 (16), p.2403-2408

2000

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Mutation and expression analysis of the putative prostate tumour-suppressor gene PTEN

British journal of cancer, 1998-11, Vol.78 (10), p.1296-1300

1998

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Pharmacogenetic studies of epilepsy drugs: are we there yet?

Trends in genetics, 2006-05, Vol.22 (5), p.250-252

Spurr, Nigel K.

2006

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A first-generation whole genome-radiation hybrid map spanning the mouse genome

Genome research, 1997-12, Vol.7 (12), p.1153-1161

1997

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Single nucleotide polymorphisms as tools in human genetics

Human molecular genetics, 2000-10, Vol.9 (16), p.2403-2408

2000

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Loss of the chromosomal region 10q23-25 in prostate cancer

Cancer research (Chicago, Ill.), 1995-11, Vol.55 (21), p.4800-4803

1995

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Germline Mutations of the CDKN2 Gene in UK Melanoma Families

Human molecular genetics, 1997-11, Vol.6 (12), p.2061-2067

1997

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A Gilbert's syndrome UGT1A1 variant confers susceptibility to tranilast-induced hyperbilirubinemia

The pharmacogenomics journal, 2004-01, Vol.4 (1), p.49-53

2004

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Genetics of calcium-sensing — regulation of calcium levels in the body

Current opinion in pharmacology, 2003-06, Vol.3 (3), p.291-294

Spurr, Nigel K

2003

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Debrisoquine hydroxylase gene polymorphism and susceptibility to Parkinson's disease

The Lancet (British edition), 1992-06, Vol.339 (8806), p.1375-1377

1992

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Chromosomal localization of human genes for arylamine N-acetyltransferase

Biochemical journal, 1994-02, Vol.297 (3), p.441-445

1994

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Abnormal expression of wild type p53 protein in normal cells of a cancer family patient

The Lancet (British edition), 1992-08, Vol.340 (8814), p.259-263

1992

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Simple repeat sequences on the human Y chromosome are equally polymorphic as their autosomal counterparts

Human genetics, 1992-06, Vol.89 (4), p.389-394

1992

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Identification of the primary gene defect at the cytochrome P450 CYP2D locus

Nature (London), 1990-10, Vol.347 (6295), p.773-776

1990

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A 2.4-Megabase Physical Map Spanning the CYP2C Gene Cluster on Chromosome 10q24

Genomics (San Diego, Calif.), 1995-07, Vol.28 (2), p.328-332

1995

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Localization of the gene for familial adenomatous polyposis on chromosome 5

Nature (London), 1987-08, Vol.328 (6131), p.614-616

1987

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The Lutheran Blood Group Glycoprotein, Another Member of the Immunoglobulin Superfamily, is Widely Expressed in Human Tissues and is Developmentally Regulated in Human Liver

Proceedings of the National Academy of Sciences - PNAS, 1995-06, Vol.92 (12), p.5496-5500

1995

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Identification of two new Pmp22 mouse mutants using large-scale mutagenesis and a novel rapid mapping strategy

Human molecular genetics, 2000-07, Vol.9 (12), p.1865-1871

2000

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An autosomal transcript in skeletal muscle with homology to dystrophin

Nature (London), 1989-05, Vol.339 (6219), p.55-58

1989

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Glutathione S-transferase mu locus: use of genotyping and phenotyping assays to assess association with lung cancer susceptibility

Carcinogenesis (New York), 1991-09, Vol.12 (9), p.1533-1537

1991

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Mutation of Celsr1 Disrupts Planar Polarity of Inner Ear Hair Cells and Causes Severe Neural Tube Defects in the Mouse

Current biology, 2003-07, Vol.13 (13), p.1129-1133

2003

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Epoxy Nanocomposites Based on the Synthetic α-Zirconium Phosphate Layer Structure

Relationship between the GSTM1 genetic polymorphism and susceptibility to bladder, breast and colon cancer

Plectin deficiency results in muscular dystrophy with epidermolysis bullosa

Multifactorial Analysis of Differences Between Sporadic Breast Cancers and Cancers Involving BRCA1 and BRCA2 Mutations

Single nucleotide polymorphisms as tools in human genetics

Mutation and expression analysis of the putative prostate tumour-suppressor gene PTEN

Pharmacogenetic studies of epilepsy drugs: are we there yet?

A first-generation whole genome-radiation hybrid map spanning the mouse genome

Single nucleotide polymorphisms as tools in human genetics

Loss of the chromosomal region 10q23-25 in prostate cancer

Germline Mutations of the CDKN2 Gene in UK Melanoma Families

A Gilbert's syndrome UGT1A1 variant confers susceptibility to tranilast-induced hyperbilirubinemia

Genetics of calcium-sensing — regulation of calcium levels in the body

Debrisoquine hydroxylase gene polymorphism and susceptibility to Parkinson's disease

Chromosomal localization of human genes for arylamine N-acetyltransferase

Abnormal expression of wild type p53 protein in normal cells of a cancer family patient

Simple repeat sequences on the human Y chromosome are equally polymorphic as their autosomal counterparts

Identification of the primary gene defect at the cytochrome P450 CYP2D locus

A 2.4-Megabase Physical Map Spanning the CYP2C Gene Cluster on Chromosome 10q24

Localization of the gene for familial adenomatous polyposis on chromosome 5

The Lutheran Blood Group Glycoprotein, Another Member of the Immunoglobulin Superfamily, is Widely Expressed in Human Tissues and is Developmentally Regulated in Human Liver

Identification of two new Pmp22 mouse mutants using large-scale mutagenesis and a novel rapid mapping strategy

An autosomal transcript in skeletal muscle with homology to dystrophin

Glutathione S-transferase mu locus: use of genotyping and phenotyping assays to assess association with lung cancer susceptibility

Mutation of Celsr1 Disrupts Planar Polarity of Inner Ear Hair Cells and Causes Severe Neural Tube Defects in the Mouse

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