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Incidence of Hereditary Nonpolyposis Colorectal Cancer and the Feasibility of Molecular Screening for the Disease

The New England journal of medicine, 1998-05, Vol.338 (21), p.1481-1487

1998

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Microarray analysis of gene expression during the inflammation and endochondral bone formation stages of rat femur fracture repair

Bone (New York, N.Y.), 2006-04, Vol.38 (4), p.521-529

2006

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Single-Nucleotide Polymorphisms (SNPs) in Human β-Defensin 1: High-Throughput SNP Assays and Association with Candida Carriage in Type I Diabetics and Nondiabetic Controls

Journal of Clinical Microbiology, 2003-01, Vol.41 (1), p.90-96

2003

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Loss of Imprinting of the Insulin-Like Growth Factor II Gene Occurs by Biallelic Methylation in a Core Region of H19-Associated CTCF-binding Sites in Colorectal Cancer

Proceedings of the National Academy of Sciences - PNAS, 2001-01, Vol.98 (2), p.591-596

2001

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Global gene expression analysis in the bones reveals involvement of several novel genes and pathways in mediating an anabolic response of mechanical loading in mice

Journal of cellular biochemistry, 2005-12, Vol.96 (5), p.1049-1060

2005

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Tumor formation and inactivation of RIZ1, an Rb-binding member of a nuclear protein-methyltransferase superfamily

Genes & development, 2001-09, Vol.15 (17), p.2250-2262

2001

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Conversion of diploidy to haploidy: Individuals susceptible to multigene disorders may now be spotted more easily

Nature (London), 2000-02, Vol.403 (6771), p.723-724

2000

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Candidate Tumor Suppressor RIZ Is Frequently Involved in Colorectal Carcinogenesis

Proceedings of the National Academy of Sciences - PNAS, 2000-03, Vol.97 (6), p.2662-2667

2000

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Spontaneous Fractures in the Mouse Mutant sfx Are Caused by Deletion of the Gulonolactone Oxidase Gene, Causing Vitamin C Deficiency

Journal of bone and mineral research, 2005-09, Vol.20 (9), p.1597-1610

2005

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Semiautomated assessment of loss of heterozygosity and replication error in tumors

Cancer research (Chicago, Ill.), 1996-07, Vol.56 (14), p.3331-3337

1996

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EGFR and EGFRvIII expression in primary breast cancer and cell lines

Breast cancer research and treatment, 2004-09, Vol.87 (1), p.87-95

2004

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Mutations in CUBN , encoding the intrinsic factor-vitamin B 12 receptor, cubilin, cause hereditary megaloblastic anaemia 1

Nature genetics, 1999-03, Vol.21 (3), p.309-313

1999

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A Polymorphism in the CYP17 Gene and Risk of Prostate Cancer

Cancer epidemiology, biomarkers & prevention, 2002-03, Vol.11 (3), p.243-247

2002

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Synergistic activation of the insulin gene by a LIM-homeo domain protein and a basic helix-loop-helix protein : building a functional insulin minienhancer complex

Genes & development, 1992-11, Vol.6 (11), p.2165-2176

1992

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Polymorphic Variation at the BAT-25 and BAT-26 Loci in Individuals of African Origin : Implications for Microsatellite Instability Testing

The American journal of pathology, 1999-08, Vol.155 (2), p.349-353

1999

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Recurrent germline mutation in MSH2 arises frequently de novo

Journal of medical genetics, 2000-09, Vol.37 (9), p.646-652

2000

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MSH6 and MSH3 are rarely involved in genetic predisposition to nonpolypotic colon cancer

Cancer research (Chicago, Ill.), 2001-02, Vol.61 (4), p.1619-1623

2001

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Hereditary and somatic DNA mismatch repair gene mutations in sporadic endometrial carcinoma

Journal of medical genetics, 2001-07, Vol.38 (7), p.461-466

2001

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The I1307K polymorphism of the APC gene in colorectal cancer

Gastroenterology (New York, N.Y. 1943), 1999, Vol.116 (1), p.58-63

1999

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Hybrids monosomal for human chromosome 5 reveal the presence of a spinal muscular atrophy (SMA) carrier with two SMN1 copies on one chromosome

Human genetics, 2001-02, Vol.108 (2), p.109-115

2001

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Heterozygote and mutation detection by direct automated fluorescent DNA sequencing using a mutant Taq DNA polymerase

BioTechniques, 1996-04, Vol.20 (4), p.676-683

1996

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Data processing algorithms used by NOAA's wind profiler demonstration network

Annales geophysicae (1988), 1994-05, Vol.12 (6), p.518-528

1994

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Efficient, automatic detection of heterozygous bases during large-scale DNA sequence screening

BioTechniques, 1995-12, Vol.19 (6), p.984

1995

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Aqueous Chemistry of Element 105

Radiochimica acta, 1988-04, Vol.43 (4), p.223-232

1988

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Direct proof of electron-capture-delayed-fission process

Physical review letters, 1989-12, Vol.63 (23), p.2548-2550

1989

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Incidence of Hereditary Nonpolyposis Colorectal Cancer and the Feasibility of Molecular Screening for the Disease

Microarray analysis of gene expression during the inflammation and endochondral bone formation stages of rat femur fracture repair

Single-Nucleotide Polymorphisms (SNPs) in Human β-Defensin 1: High-Throughput SNP Assays and Association with Candida Carriage in Type I Diabetics and Nondiabetic Controls

Loss of Imprinting of the Insulin-Like Growth Factor II Gene Occurs by Biallelic Methylation in a Core Region of H19-Associated CTCF-binding Sites in Colorectal Cancer

Global gene expression analysis in the bones reveals involvement of several novel genes and pathways in mediating an anabolic response of mechanical loading in mice

Tumor formation and inactivation of RIZ1, an Rb-binding member of a nuclear protein-methyltransferase superfamily

Conversion of diploidy to haploidy: Individuals susceptible to multigene disorders may now be spotted more easily

Candidate Tumor Suppressor RIZ Is Frequently Involved in Colorectal Carcinogenesis

Spontaneous Fractures in the Mouse Mutant sfx Are Caused by Deletion of the Gulonolactone Oxidase Gene, Causing Vitamin C Deficiency

Semiautomated assessment of loss of heterozygosity and replication error in tumors

EGFR and EGFRvIII expression in primary breast cancer and cell lines

Mutations in CUBN , encoding the intrinsic factor-vitamin B 12 receptor, cubilin, cause hereditary megaloblastic anaemia 1

A Polymorphism in the CYP17 Gene and Risk of Prostate Cancer

Synergistic activation of the insulin gene by a LIM-homeo domain protein and a basic helix-loop-helix protein : building a functional insulin minienhancer complex

Polymorphic Variation at the BAT-25 and BAT-26 Loci in Individuals of African Origin : Implications for Microsatellite Instability Testing

Recurrent germline mutation in MSH2 arises frequently de novo

MSH6 and MSH3 are rarely involved in genetic predisposition to nonpolypotic colon cancer

Hereditary and somatic DNA mismatch repair gene mutations in sporadic endometrial carcinoma

The I1307K polymorphism of the APC gene in colorectal cancer

Hybrids monosomal for human chromosome 5 reveal the presence of a spinal muscular atrophy (SMA) carrier with two SMN1 copies on one chromosome

Heterozygote and mutation detection by direct automated fluorescent DNA sequencing using a mutant Taq DNA polymerase

Data processing algorithms used by NOAA's wind profiler demonstration network

Efficient, automatic detection of heterozygous bases during large-scale DNA sequence screening

Aqueous Chemistry of Element 105

Direct proof of electron-capture-delayed-fission process

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