(Q34929905)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23938146%20AND%20SRC:MED&resulttype=core&format=json

7 March 2020

title

Hereditary lissencephaly and cerebellar hypoplasia in Churra lambs (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23938146%20AND%20SRC:MED&resulttype=core&format=json

7 March 2020

main subject

lissencephaly

0 references

cerebellar hypoplasia

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23938146%20AND%20SRC:MED&resulttype=core&format=json

7 March 2020

Aroa Suárez-Vega

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23938146%20AND%20SRC:MED&resulttype=core&format=json

7 March 2020

Miguel Fuertes

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23938146%20AND%20SRC:MED&resulttype=core&format=json

7 March 2020

Julio Benavides

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23938146%20AND%20SRC:MED&resulttype=core&format=json

María Del Carmen Ferreras Estrada

7 March 2020

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23938146%20AND%20SRC:MED&resulttype=core&format=json

7 March 2020

Juan J Arranz

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23938146%20AND%20SRC:MED&resulttype=core&format=json

7 March 2020

author name string

Laetitia Delgado

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23938146%20AND%20SRC:MED&resulttype=core&format=json

7 March 2020

publication date

9 August 2013

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23938146%20AND%20SRC:MED&resulttype=core&format=json

7 March 2020

published in

BMC Veterinary Research

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23938146%20AND%20SRC:MED&resulttype=core&format=json

7 March 2020

volume

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23938146%20AND%20SRC:MED&resulttype=core&format=json

7 March 2020

page(s)

156

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23938146%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1186/1746-6148-9-156

7 March 2020

exact match

0 references

cites work

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Role of cytoskeletal abnormalities in the neuropathology and pathophysiology of type I lissencephaly

8 July 2018

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TUBA1A mutations cause wide spectrum lissencephaly (smooth brain) and suggest that multiple neuronal migration pathways converge on alpha tubulins.

8 July 2018

1 reference

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8 July 2018

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Neuronal migration disorders

8 July 2018

1 reference

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Standardized human pedigree nomenclature: update and assessment of the recommendations of the National Society of Genetic Counselors

8 July 2018

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8 July 2018

1 reference

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Lissencephaly with agenesis of corpus callosum and rudimentary dysplastic cerebellum: a subtype of lissencephaly with cerebellar hypoplasia

8 July 2018

1 reference

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8 July 2018

1 reference

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Neuronal migration, cerebral cortical development, and cerebral cortical anomalies

8 July 2018

1 reference

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Lissencephaly with cerebellar hypoplasia (LCH): a heterogeneous group of cortical malformations

8 July 2018

1 reference

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Human brain malformations and their lessons for neuronal migration

8 July 2018

1 reference

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Role of the reelin signaling pathway in central nervous system development

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3750509

Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3750509

Neuronal migration disorders: from genetic diseases to developmental mechanisms

8 July 2018

1 reference

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Genetic malformations of the human cerebral cortex

8 July 2018

1 reference

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Reeler/Disabled-like disruption of neuronal migration in knockout mice lacking the VLDL receptor and ApoE receptor 2

8 July 2018

1 reference

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

8 July 2018

1 reference

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Birthdate and cell marker analysis of scrambler: a novel mutation affecting cortical development with a reeler-like phenotype.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3750509

Neuronal position in the developing brain is regulated by mouse disabled-1

8 July 2018

1 reference

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Lissencephaly with extreme cerebral and cerebellar hypoplasia. A magnetic resonance imaging study

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3750509

Syndromes with lissencephaly

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3750509

Neuropathology of lissencephalies

8 July 2018

1 reference

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Lissencephaly gene (LIS1) expression in the CNS suggests a role in neuronal migration

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3750509

8 July 2018

1 reference

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Pathology in the ovine foetus caused by an ovine pestivirus

8 July 2018

1 reference

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A simple salting out procedure for extracting DNA from human nucleated cells

8 July 2018

1 reference

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Ovine arthrogryposis and central nervous system malformations associated with in utero Cache Valley virus infection: spontaneous disease

8 July 2018

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Lissencephaly in Lhasa Apso dogs

8 July 2018

1 reference

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Lissencephaly in two Lhasa Apso dogs

8 July 2018

1 reference

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Neuropathological phenotype of a distinct form of lissencephaly associated with mutations in TUBA1A.

8 July 2018

1 reference

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Salient lesions in domestic ruminants infected with the emerging so-called Schmallenberg virus in Germany

21 January 2018

1 reference

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Human lissencephaly with cerebellar hypoplasia due to mutations in TUBA1A: expansion of the foetal neuropathological phenotype

21 January 2018

1 reference

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Cost-effective parentage verification with 17-plex PCR for goats and 19-plex PCR for sheep.

21 January 2018

1 reference

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Lissencephaly and microencephaly combined with hypoplasia of corpus callosum and cerebellum in a domestic cat.

21 January 2018

1 reference

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Familial lissencephaly with cleft palate and severe cerebellar hypoplasia

26 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23938146

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1746-6148-9-156

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23938146%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

7 March 2020

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23938146%20AND%20SRC:MED&resulttype=core&format=json

7 March 2020

PubMed publication ID

23938146

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23938146%20AND%20SRC:MED&resulttype=core&format=json