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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9697681
retrieved
5 February 2018
reference URL
http://europepmc.org/abstract/MED/9697681
title
LISsen up!
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9697681
retrieved
5 February 2018
reference URL
http://europepmc.org/abstract/MED/9697681
author name string
Walsh CA
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9697681
retrieved
5 February 2018
reference URL
http://europepmc.org/abstract/MED/9697681
language of work or name
English
0 references
publication date
1 August 1998
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9697681
retrieved
5 February 2018
reference URL
http://europepmc.org/abstract/MED/9697681
published in
Nature Genetics
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9697681
retrieved
5 February 2018
reference URL
http://europepmc.org/abstract/MED/9697681
volume
19
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9697681
retrieved
5 February 2018
reference URL
http://europepmc.org/abstract/MED/9697681
issue
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9697681
retrieved
5 February 2018
reference URL
http://europepmc.org/abstract/MED/9697681
page(s)
307-308
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9697681
retrieved
5 February 2018
reference URL
http://europepmc.org/abstract/MED/9697681
cites work
Graded reduction of Pafah1b1 (Lis1) activity results in neuronal migration defects and early embryonic lethality
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F1186
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Lissencephaly. A human brain malformation associated with deletion of the LIS1 gene located at chromosome 17p13.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F1186
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Lissencephaly and other malformations of cortical development: 1995 update
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F1186
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/10.1038%2F1186
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
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F1186
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Isolation of a Miller-Dieker lissencephaly gene containing G protein beta-subunit-like repeats
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F1186
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Miller-Dieker lissencephaly gene encodes a subunit of brain platelet-activating factor acetylhydrolase [corrected]
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F1186
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Reduction of microtubule catastrophe events by LIS1, platelet-activating factor acetylhydrolase subunit.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F1186
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
NudF, a nuclear migration gene in Aspergillus nidulans, is similar to the human LIS-1 gene required for neuronal migration
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F1186
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Scrambler, a new neurological mutation of the mouse with abnormalities of neuronal migration
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F1186
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Birthdate and cell marker analysis of scrambler: a novel mutation affecting cortical development with a reeler-like phenotype.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F1186
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The reeler gene encodes a protein with an EGF–like motif expressed by pioneer neurons
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F1186
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A protein related to extracellular matrix proteins deleted in the mouse mutant reeler
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F1186
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Aberrant splicing of a mouse disabled homolog, mdab1, in the scrambler mouse
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F1186
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Neuronal position in the developing brain is regulated by mouse disabled-1
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F1186
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Targeted disruption of the cyclin-dependent kinase 5 gene results in abnormal corticogenesis, neuronal pathology and perinatal death
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F1186
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mice lacking p35, a neuronal specific activator of Cdk5, display cortical lamination defects, seizures, and adult lethality
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F1186
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/1186
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9697681
retrieved
5 February 2018
reference URL
http://europepmc.org/abstract/MED/9697681
Dimensions Publication ID
1052397323
0 references
PubMed publication ID
9697681
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9697681
retrieved
5 February 2018
reference URL
http://europepmc.org/abstract/MED/9697681
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