DCAMKL1, a brain-specific transmembrane protein on 13q12.3 that is similar to doublecortin (DCX) (Q22008801)

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English	DCAMKL1, a brain-specific transmembrane protein on 13q12.3 that is similar to doublecortin (DCX)	scientific article

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instance of

scholarly article

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title

DCAMKL1, a brain-specific transmembrane protein on 13q12.3 that is similar to doublecortin (DCX) (English)

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main subject

brain

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transmembrane protein

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Doublecortin like kinase 1

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stated in

GOA release 2020-03-11

nervous system development

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stated in

GOA release 2020-03-11

author name string

K Sossey-Alaoui

series ordinal

1

author given names

K

author last names

Sossey-Alaoui

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stated in

PubMed

PubMed publication ID

10036192

retrieved

7 February 2023

A K Srivastava

series ordinal

2

author given names

A K

author last names

Srivastava

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stated in

PubMed

PubMed publication ID

10036192

retrieved

7 February 2023

language of work or name

English

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publication date

15 February 1999

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published in

Genomics

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volume

56

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issue

1

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page(s)

121-6

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cites work

Previously apparently undescribed syndrome: shallow orbits, ptosis, coloboma, trigonocephaly, gyral malformations, and mental and growth retardation

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1006%2FGENO.1998.5718

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

High-resolution YAC-cosmid-STS map of human chromosome 13.

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1006%2FGENO.1998.5718

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1006%2FGENO.1998.5718

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1006%2FGENO.1998.5718

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

A classification scheme for malformations of cortical development

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1006%2FGENO.1998.5718

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Prediction of the coding sequences of unidentified human genes. VII. The complete sequences of 100 new cDNA clones from brain which can code for large proteins in vitro

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1006%2FGENO.1998.5718

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Point mutations and an intragenic deletion in LIS1, the lissencephaly causative gene in isolated lissencephaly sequence and Miller-Dieker syndrome

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1006%2FGENO.1998.5718

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Human doublecortin (DCX) and the homologous gene in mouse encode a putative Ca2+-dependent signaling protein which is mutated in human X-linked neuronal migration defects

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1006%2FGENO.1998.5718

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

BCM Search Launcher--an integrated interface to molecular biology data base search and analysis services available on the World Wide Web.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1006%2FGENO.1998.5718

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

X-linked malformations of neuronal migration

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1006%2FGENO.1998.5718

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

DOI

10.1006/GENO.1998.5718

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PubMed publication ID

10036192

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