(Q22008668)

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Characterization of a novel gene, PNUTL2, on human chromosome 17q22-q23 and its exclusion as the Meckel syndrome gene

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Characterization of a novel gene, PNUTL2, on human chromosome 17q22-q23 and its exclusion as the Meckel syndrome gene (English)

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main subject

Septin 4

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stated in

GOA release 2020-03-11

structural molecule activity

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GOA release 2020-03-11

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P Paavola

1

P

Paavola

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PubMed

PubMed publication ID

9889007

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7 February 2023

N Horelli-Kuitunen

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2

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Horelli-Kuitunen

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PubMed

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9889007

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7 February 2023

A Palotie

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3

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A

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Palotie

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PubMed

PubMed publication ID

9889007

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7 February 2023

L Peltonen

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L

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Peltonen

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PubMed publication ID

9889007

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language of work or name

English

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publication date

1 January 1999

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published in

Genomics

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volume

55

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issue

1

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page(s)

122-5

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cites work

Genetic control of the cell division cycle in yeast *1IV. Genes controlling bud emergence and cytokinesis

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https://api.crossref.org/works/10.1006%2FGENO.1998.5612

retrieved

7 January 2021

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Fiber-FISH: experiences and a refined protocol

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reference URL

https://api.crossref.org/works/10.1006%2FGENO.1998.5612

retrieved

7 January 2021

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The locus for Meckel syndrome with multiple congenital anomalies maps to chromosome 17q21-q24.

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reference URL

https://api.crossref.org/works/10.1006%2FGENO.1998.5612

retrieved

7 January 2021

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Localization and possible functions of Drosophila septins.

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reference URL

https://api.crossref.org/works/10.1006%2FGENO.1998.5612

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Ultra-sensitive FISH using peroxidase-mediated deposition of biotin- or fluorochrome tyramides.

1 reference

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https://api.crossref.org/works/10.1006%2FGENO.1998.5612

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7 January 2021

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A Collection of cDNA Clones with Specific Expression Patterns in Mouse Brain

1 reference

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reference URL

https://api.crossref.org/works/10.1006%2FGENO.1998.5612

retrieved

7 January 2021

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Alternative expression of platelet glycoprotein Ib(beta) mRNA from an adjacent 5' gene with an imperfect polyadenylation signal sequence

1 reference

stated in

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reference URL

https://api.crossref.org/works/10.1006%2FGENO.1998.5612

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

DOI

10.1006/GENO.1998.5612

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PubMed publication ID

9889007

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(Q22008668)

Characterization of a novel gene, PNUTL2, on human chromosome 17q22-q23 and its exclusion as the Meckel syndrome gene

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