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Human prostate cancer and benign prostatic hyperplasia : Molecular dissection by gene expression profiling

Cancer research (Chicago, Ill.), 2001-06, Vol.61 (12), p.4683-4688

2001

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Detection of gene amplification by genomic hybridization to cDNA microarrays

Cancer research (Chicago, Ill.), 2000-02, Vol.60 (4), p.799-802

2000

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Linkage Analyses at the Chromosome 1 Loci 1q24-25 (HPC1), 1q42.2-43 (PCAP), and 1p36 (CAPB) in Families with Hereditary Prostate Cancer

American journal of human genetics, 2000-02, Vol.66 (2), p.539-546

2000

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The association of chromosome 8p deletion and tumor metastasis in human hepatocellular carcinoma

Cancer research (Chicago, Ill.), 1999-11, Vol.59 (22), p.5662-5665

1999

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Hybrid selection of transcribed sequences from microdissected DNA : Isolation of genes within an amplified region at 20q11-q13.2 in breast cancer

Cancer research (Chicago, Ill.), 1996-08, Vol.56 (15), p.3446-3450

1996

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Linkage of prostate cancer susceptibility loci to chromosome 1

Human genetics, 2001-04, Vol.108 (4), p.335-345

2001

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Gene expression profile in multiple sclerosis patients and healthy controls: identifying pathways relevant to disease

Human molecular genetics, 2003-09, Vol.12 (17), p.2191-2199

2003

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Report of the committee on structural chromosome changes in neoplasia

Cytogenetics and cell genetics, 1989, Vol.51 (1-4), p.533

1989

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Identification of cryptic sites of DNA sequence amplification in human breast cancer by chromosome microdissection

Nature genetics, 1994-10, Vol.8 (2), p.155-161

1994

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Clustering of Non-Major Histocompatibility Complex Susceptibility Candidate Loci in Human Autoimmune Diseases

Proceedings of the National Academy of Sciences - PNAS, 1998-08, Vol.95 (17), p.9979-9984

1998

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Identification by Representational Difference Analysis of a Homozygous Deletion in Pancreatic Carcinoma that Lies within the BRCA2 Region

Proceedings of the National Academy of Sciences - PNAS, 1995-06, Vol.92 (13), p.5950-5954

1995

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Ratio statistics of gene expression levels and applications to microarray data analysis

Bioinformatics (Oxford, England), 2002-09, Vol.18 (9), p.1207-1215

2002

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Stress-specific signatures: expression profiling of p53 wild-type and -null human cells

Oncogene, 2005-06, Vol.24 (28), p.4572-4579

2005

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Early age at diagnosis in families providing evidence of linkage to the hereditary prostate cancer locus (HPC1) on chromosome 1

Cancer research (Chicago, Ill.), 1997-11, Vol.57 (21), p.4707-4709

1997

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Effects of RNase L mutations associated with prostate cancer on apoptosis induced by 2', 5'-oligoadenylates

Cancer research (Chicago, Ill.), 2003-10, Vol.63 (20), p.6795-6801

2003

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Tumorigenicity in Human Melanoma Cell Lines Controlled by Introduction of Human Chromosome 6

Science (American Association for the Advancement of Science), 1990-02, Vol.247 (4942), p.568-571

1990

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cDNA Microarrays Detect Activation of a Myogenic Transcription Program by the PAX3-FKHR Fusion Oncogene

Proceedings of the National Academy of Sciences - PNAS, 1999-11, Vol.96 (23), p.13264-13269

1999

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Gene-expression profiling in human cutaneous melanoma

Oncogene, 2003-05, Vol.22 (20), p.3076-3080

2003

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The Human Gastrin/Cholecystokinin Type B Receptor Gene: Alternative Splice Donor Site in Exon 4 Generates Two Variant mRNAs

Proceedings of the National Academy of Sciences - PNAS, 1993-10, Vol.90 (19), p.9085-9089

1993

Volltextzugriff (PDF)

CACP , encoding a secreted proteoglycan, is mutated in camptodactyly-arthropathy-coxa vara-pericarditis syndrome

Nature genetics, 1999-11, Vol.23 (3), p.319-322

1999

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Identification of an Amplified, Highly Expressed Gene in a Human Glioma

Science (American Association for the Advancement of Science), 1987-04, Vol.236 (4797), p.70-73

1987

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Heterogeneity of genetic alterations in prostate cancer : evidence of the complex nature of the disease

Human molecular genetics, 2001-10, Vol.10 (20), p.2313-2318

2001

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Evidence for a prostate cancer linkage to chromosome 20 in 159 hereditary prostate cancer families

Human genetics, 2001-05, Vol.108 (5), p.430-435

2001

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A common nonsense mutation in EphB2 is associated with prostate cancer risk in African American men with a positive family history

Journal of medical genetics, 2006-06, Vol.43 (6), p.507-511

2006

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Major Susceptibility Locus for Prostate Cancer on Chromosome 1 Suggested by a Genome-Wide Search

Science (American Association for the Advancement of Science), 1996-11, Vol.274 (5291), p.1371-1374

1996

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Human prostate cancer and benign prostatic hyperplasia : Molecular dissection by gene expression profiling

Detection of gene amplification by genomic hybridization to cDNA microarrays

Linkage Analyses at the Chromosome 1 Loci 1q24-25 (HPC1), 1q42.2-43 (PCAP), and 1p36 (CAPB) in Families with Hereditary Prostate Cancer

The association of chromosome 8p deletion and tumor metastasis in human hepatocellular carcinoma

Hybrid selection of transcribed sequences from microdissected DNA : Isolation of genes within an amplified region at 20q11-q13.2 in breast cancer

Linkage of prostate cancer susceptibility loci to chromosome 1

Gene expression profile in multiple sclerosis patients and healthy controls: identifying pathways relevant to disease

Report of the committee on structural chromosome changes in neoplasia

Identification of cryptic sites of DNA sequence amplification in human breast cancer by chromosome microdissection

Clustering of Non-Major Histocompatibility Complex Susceptibility Candidate Loci in Human Autoimmune Diseases

Identification by Representational Difference Analysis of a Homozygous Deletion in Pancreatic Carcinoma that Lies within the BRCA2 Region

Ratio statistics of gene expression levels and applications to microarray data analysis

Stress-specific signatures: expression profiling of p53 wild-type and -null human cells

Early age at diagnosis in families providing evidence of linkage to the hereditary prostate cancer locus (HPC1) on chromosome 1

Effects of RNase L mutations associated with prostate cancer on apoptosis induced by 2', 5'-oligoadenylates

Tumorigenicity in Human Melanoma Cell Lines Controlled by Introduction of Human Chromosome 6

cDNA Microarrays Detect Activation of a Myogenic Transcription Program by the PAX3-FKHR Fusion Oncogene

Gene-expression profiling in human cutaneous melanoma

The Human Gastrin/Cholecystokinin Type B Receptor Gene: Alternative Splice Donor Site in Exon 4 Generates Two Variant mRNAs

CACP , encoding a secreted proteoglycan, is mutated in camptodactyly-arthropathy-coxa vara-pericarditis syndrome

Identification of an Amplified, Highly Expressed Gene in a Human Glioma

Heterogeneity of genetic alterations in prostate cancer : evidence of the complex nature of the disease

Evidence for a prostate cancer linkage to chromosome 20 in 159 hereditary prostate cancer families

A common nonsense mutation in EphB2 is associated with prostate cancer risk in African American men with a positive family history

Major Susceptibility Locus for Prostate Cancer on Chromosome 1 Suggested by a Genome-Wide Search

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