(Q28258611)

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Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinase

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scholarly article

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Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinase (English)

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Peutz-Jeghers syndrome

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author name string

D E Jenne

1

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H Reimann

2

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J Nezu

3

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W Friedel

4

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S Loff

5

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R Jeschke

6

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O Müller

7

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W Back

8

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M Zimmer

9

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language of work or name

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publication date

January 1998

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Nature Genetics

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18

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1

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38-43

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Increased risk of cancer in the Peutz-Jeghers syndrome

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https://api.crossref.org/works/10.1038%2FNG0198-38

7 January 2021

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Cancer and the Peutz-Jeghers syndrome

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https://api.crossref.org/works/10.1038%2FNG0198-38

7 January 2021

based on heuristic

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Localization of a susceptibility locus for Peutz-Jeghers syndrome to 19p using comparative genomic hybridization and targeted linkage analysis

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https://api.crossref.org/works/10.1038%2FNG0198-38

7 January 2021

based on heuristic

inferred from DOI database lookup

An integrated metric physical map of human chromosome 19.

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https://api.crossref.org/works/10.1038%2FNG0198-38

7 January 2021

based on heuristic

inferred from DOI database lookup

A Gene Map of the Human Genome

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https://api.crossref.org/works/10.1038%2FNG0198-38

7 January 2021

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Conserved sequences in a class of rare eukaryotic nuclear introns with non-consensus splice sites

1 reference

https://api.crossref.org/works/10.1038%2FNG0198-38

7 January 2021

based on heuristic

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Cloning and characterization of a novel serine/threonine protein kinase expressed in early Xenopus embryos

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https://api.crossref.org/works/10.1038%2FNG0198-38

7 January 2021

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The eukaryotic protein kinase superfamily: kinase (catalytic) domain structure and classification 1

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https://api.crossref.org/works/10.1038%2FNG0198-38

7 January 2021

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Identification of a candidate tumour suppressor gene, MMAC1, at chromosome 10q23.3 that is mutated in multiple advanced cancers

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https://api.crossref.org/works/10.1038%2FNG0198-38

7 January 2021

based on heuristic

inferred from DOI database lookup

Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome

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https://api.crossref.org/works/10.1038%2FNG0198-38

7 January 2021

based on heuristic

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Mutations of chromosome 5q21 genes in FAP and colorectal cancer patients

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https://api.crossref.org/works/10.1038%2FNG0198-38

7 January 2021

based on heuristic

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Identification of deletion mutations and three new genes at the familial polyposis locus

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https://api.crossref.org/works/10.1038%2FNG0198-38

7 January 2021

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PTEN, a putative protein tyrosine phosphatase gene mutated in human brain, breast, and prostate cancer

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https://api.crossref.org/works/10.1038%2FNG0198-38

7 January 2021

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Identification of a Gene Located at Chromosome 5q21 that Is Mutated in Colorectal Cancers

1 reference

https://api.crossref.org/works/10.1038%2FNG0198-38

7 January 2021

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Three human elastase-like genes coordinately expressed in the myelomonocyte lineage are organized as a single genetic locus on 19pter

1 reference

https://api.crossref.org/works/10.1038%2FNG0198-38

7 January 2021

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The human Met-ase gene (GZMM): structure, sequence, and close physical linkage to the serine protease gene cluster on 19p13.3

1 reference

https://api.crossref.org/works/10.1038%2FNG0198-38

7 January 2021

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Analysis of cosmids using linearization by phage lambda terminase

1 reference

https://api.crossref.org/works/10.1038%2FNG0198-38

7 January 2021

based on heuristic

inferred from DOI database lookup

[Peutz-Jeghers syndrome. Cases at the Mannheim clinic over 25 years]

1 reference

https://api.crossref.org/works/10.1038%2FNG0198-38

7 January 2021

based on heuristic

inferred from DOI database lookup

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