Germline sequence variants of the LZTS1 gene are associated with prostate cancer risk (Q34154269)

31 July 2017

title

Germline sequence variants of the LZTS1 gene are associated with prostate cancer risk (English)

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31 July 2017

11

Eugene R Bleecker

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31 July 2017

15

Jianfeng Xu

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31 July 2017

14

William B Isaacs

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31 July 2017

2

Josyf C Mychaleckyj

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7

Kathleen E Wiley

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31 July 2017

1

Gregory A Hawkins

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4

Dennis A Faith

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31 July 2017

10

Piroska Bujnovszky

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31 July 2017

Siqun L Zheng

3

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31 July 2017

Brian Kelly

5

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31 July 2017

S D Isaacs

6

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31 July 2017

Bao-Li Chang

8

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31 July 2017

Charles M Ewing

9

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P C Walsh

12

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31 July 2017

Deborah A Meyers

13

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31 July 2017

publication date

1 August 2002

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Cancer Genetics and Cytogenetics

31 July 2017

published in

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31 July 2017

volume

137

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31 July 2017

issue

1

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31 July 2017

page(s)

1-7

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Physical mapping of chromosome 8p22 markers and their homozygous deletion in a metastatic prostate cancer.

31 July 2017

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Linkage and association studies of prostate cancer susceptibility: evidence for linkage at 8p22-23

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Evidence for a rare prostate cancer-susceptibility locus at chromosome 1p36.

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Model-free linkage analysis with covariates confirms linkage of prostate cancer to chromosomes 1 and 4.

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Structure and methylation-associated silencing of a gene within a homozygously deleted region of human chromosome band 8p22.

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7 January 2021

Tumour-suppressor genes in prostatic oncogenesis: a positional approach

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7 January 2021

The FEZ1 gene at chromosome 8p22 encodes a leucine-zipper protein, and its expression is altered in multiple human tumors

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7 January 2021

Functional identification of LZTS1 as a candidate prostate tumor suppressor gene on human chromosome 8p22.

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FEZ1/LZTS1 gene at 8p22 suppresses cancer cell growth and regulates mitosis

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7 January 2021

Exact tests for association between alleles at arbitrary numbers of loci

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Biased distribution of inverted and direct Alus in the human genome: implications for insertion, exclusion, and genome stability.

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Primary chromosomal rearrangements of leukemia are frequently accompanied by extensive submicroscopic deletions and may lead to altered prognosis

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An Alu-mediated 7.1 kb deletion of BRCA1 exons 8 and 9 in breast and ovarian cancer families that results in alternative splicing of exon 10

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An Alu cassette in the cytoplasmic domain of an interferon receptor subunit

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7 January 2021

Identification of a 14 kb deletion involving the promoter region of BRCA1 in a breast cancer family

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7 January 2021

Olfactory receptor-gene clusters, genomic-inversion polymorphisms, and common chromosome rearrangements

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7 January 2021

10.1016/S0165-4608(02)00549-6

Identifiers

DOI

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31 July 2017

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