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Loss of heterozygosity of chromosome 3p markers in small-cell lung cancer

Nature (London), 1987-10, Vol.329 (6138), p.451-454

1987

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Myotonic Dystrophy Type 2 Caused by a CCTG Expansion in Intron 1 of ZNF9

Science (American Association for the Advancement of Science), 2001-08, Vol.293 (5531), p.864-867

2001

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Promise and challenge: Markers of prostate cancer detection, diagnosis and prognosis

Disease markers, 2004, Vol.20 (2), p.117-128

2004

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Structure and variability of human chromosome ends

Molecular and Cellular Biology, 1990-02, Vol.10 (2), p.518-527

1990

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A homozygous deletion on chromosome 3 in a small cell lung cancer cell line correlates with a region of tumor suppressor activity

Oncogene, 1993-07, Vol.8 (7), p.1721-1729

1993

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Localization of a novel tumor suppressor locus on human chromosome 3q important in osteosarcoma tumorigenesis

Cancer research (Chicago, Ill.), 1997, Vol.57 (1), p.106-109

1997

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Physical and functional mapping of a tumor suppressor locus for renal Cell carcinoma within chromosome 3p12

Cancer research (Chicago, Ill.), 1998-08, Vol.58 (16), p.3533-3537

1998

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Identification of a Putative Regulatory Subunit of a Calcium-Activated Potassium Channel in the dup(3q) Syndrome Region and a Related Sequence on 22q11.2

Genomics (San Diego, Calif.), 1999-11, Vol.62 (1), p.90-94

1999

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Deletions of the Short Arm of Chromosome 3 in Solid Tumors and the Search for Suppressor Genes

Advances in Cancer Research, 1997, Vol.71, p.27-92

1997

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Altered structure and expression of the human retinoblastoma susceptibility gene in small cell lung cancer

Cancer research (Chicago, Ill.), 1990-05, Vol.50 (10), p.3067-3072

1990

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Localization of the Fanconi Anemia Complementation Group D Gene to a 200-kb Region on Chromosome 3p25.3

American journal of human genetics, 2000-05, Vol.66 (5), p.1540-1551

2000

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Human Transferrin: cDNA Characterization and Chromosomal Localization

Proceedings of the National Academy of Sciences - PNAS, 1984-05, Vol.81 (9), p.2752-2756

1984

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Modulation of Disease Severity of Dystrophic Epidermolysis Bullosa By a Splice Site Mutation in Combination with a Missense Mutation in the COL7A1 Gene

Human molecular genetics, 1997-07, Vol.6 (7), p.1125-1135

1997

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Restriction fragment length polymorphism studies show consistent loss of chromosome 3p alleles in small cell lung cancer patients' tumors

The Journal of clinical investigation, 1988-08, Vol.82 (2), p.502-507

1988

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Specific expression of the annexin VIII gene in acute promyelocytic leukemia

Blood, 1992-04, Vol.79 (7), p.1802-1810

1992

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Retention of Chromosome 3 in Extrapulmonary Small Cell Cancer Shown by Molecular and Cytogenetic Studies

JNCI : Journal of the National Cancer Institute, 1989-08, Vol.81 (16), p.1223-1228

1989

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Effect of inter-miniband tunneling on current resonances due to the formation of stochastic conduction networks in superlattices

Physica. E, Low-dimensional systems & nanostructures, 2006-05, Vol.32 (1), p.285-288

2006

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Prostate Cancer and Prostate-Specific Antigen: The More We Know, the Less We Understand

JNCI : Journal of the National Cancer Institute, 2003-07, Vol.95 (14), p.1027-1028

2003

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Localization of human SAA gene(s) to chromosome 11 and detection of DNA polymorphisms

Biochemical and biophysical research communications, 1986-06, Vol.137 (3), p.1196-1204

1986

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The DNF15S2 locus at 3p21 is transcribed in normal lung and small cell lung cancer

Genomics (San Diego, Calif.), 1989-04, Vol.4 (3), p.355-361

1989

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Localization of the human prealbumin gene to chromosome 18

Biochemical and biophysical research communications, 1985-06, Vol.129 (3), p.753-758

1985

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Mapping 638 STSs to regions of human chromosome 3

Cytogenetic and genome research, 1996, Vol.72 (1), p.90-94

1996

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DNA Polymorphic Loci Mapped to Human Chromosomes 3, 5, 9, 11, 17, 18, and 22

Proceedings of the National Academy of Sciences - PNAS, 1984-04, Vol.81 (8), p.2447-2451

1984

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Loss of Heterozygosity in Breast Cancer: Cause or Effect?

JNCI : Journal of the National Cancer Institute, 1989-12, Vol.81 (23), p.1764-1765

1989

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Loss of heterozygosity of chromosome 3p markers in small-cell lung cancer

Myotonic Dystrophy Type 2 Caused by a CCTG Expansion in Intron 1 of ZNF9

Promise and challenge: Markers of prostate cancer detection, diagnosis and prognosis

Structure and variability of human chromosome ends

A homozygous deletion on chromosome 3 in a small cell lung cancer cell line correlates with a region of tumor suppressor activity

Localization of a novel tumor suppressor locus on human chromosome 3q important in osteosarcoma tumorigenesis

Physical and functional mapping of a tumor suppressor locus for renal Cell carcinoma within chromosome 3p12

Identification of a Putative Regulatory Subunit of a Calcium-Activated Potassium Channel in the dup(3q) Syndrome Region and a Related Sequence on 22q11.2

Deletions of the Short Arm of Chromosome 3 in Solid Tumors and the Search for Suppressor Genes

Altered structure and expression of the human retinoblastoma susceptibility gene in small cell lung cancer

Localization of the Fanconi Anemia Complementation Group D Gene to a 200-kb Region on Chromosome 3p25.3

Human Transferrin: cDNA Characterization and Chromosomal Localization

Modulation of Disease Severity of Dystrophic Epidermolysis Bullosa By a Splice Site Mutation in Combination with a Missense Mutation in the COL7A1 Gene

Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer

Restriction fragment length polymorphism studies show consistent loss of chromosome 3p alleles in small cell lung cancer patients' tumors

Specific expression of the annexin VIII gene in acute promyelocytic leukemia

Retention of Chromosome 3 in Extrapulmonary Small Cell Cancer Shown by Molecular and Cytogenetic Studies

Effect of inter-miniband tunneling on current resonances due to the formation of stochastic conduction networks in superlattices

Prostate Cancer and Prostate-Specific Antigen: The More We Know, the Less We Understand

Localization of human SAA gene(s) to chromosome 11 and detection of DNA polymorphisms

The DNF15S2 locus at 3p21 is transcribed in normal lung and small cell lung cancer

Localization of the human prealbumin gene to chromosome 18

Mapping 638 STSs to regions of human chromosome 3

DNA Polymorphic Loci Mapped to Human Chromosomes 3, 5, 9, 11, 17, 18, and 22

Loss of Heterozygosity in Breast Cancer: Cause or Effect?

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