(Q28587017)

English

Genetic background changes the pattern of forebrain commissure defects in transgenic mice underexpressing the beta-amyloid-precursor protein

scientific journal article

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scholarly article

1 reference

PubMed publication ID

31 January 2017

Genetic background changes the pattern of forebrain commissure defects in transgenic mice underexpressing the beta-amyloid-precursor protein (English)

1 reference

PubMed publication ID

31 January 2017

0 references

Amyloid beta (A4) precursor protein

1 reference

GOA release 2020-03-11

author name string

F. Magara

1

1 reference

PubMed publication ID

31 January 2017

U. Müller

2

1 reference

PubMed publication ID

31 January 2017

Z. W. Li

3

1 reference

PubMed publication ID

31 January 2017

H. P. Lipp

4

1 reference

PubMed publication ID

31 January 2017

C. Weissmann

5

1 reference

PubMed publication ID

31 January 2017

M. Stagljar

6

1 reference

PubMed publication ID

31 January 2017

D. P. Wolfer

7

1 reference

PubMed publication ID

31 January 2017

language of work or name

0 references

publication date

13 April 1999

1 reference

PubMed publication ID

31 January 2017

Proceedings of the National Academy of Sciences of the United States of America

1 reference

PubMed publication ID

31 January 2017

96

1 reference

PubMed publication ID

31 January 2017

8

1 reference

PubMed publication ID

31 January 2017

4656–4661

1 reference

PubMed publication ID

31 January 2017

Neurobehavioral development, adult openfield exploration and swimming navigation learning in mice with a modified beta-amyloid precursor protein gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16388

17 March 2017

Phenotype of mice lacking functional Deleted in colorectal cancer (Dcc) gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16388

17 March 2017

Sek4 and Nuk receptors cooperate in guidance of commissural axons and in palate formation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16388

17 March 2017

Behavioral and anatomical deficits in mice homozygous for a modified beta-amyloid precursor protein gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16388

17 March 2017

beta-Amyloid precursor protein-deficient mice show reactive gliosis and decreased locomotor activity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16388

17 March 2017

Netrin-1 is required for commissural axon guidance in the developing vertebrate nervous system

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16388

7 April 2017

Impaired fetal T cell development and perinatal lethality in mice lacking the cAMP response element binding protein

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16388

29 September 2017

Genetic variation among 129 substrains and its importance for targeted mutagenesis in mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16388

29 September 2017

Gene-targeting studies of mammalian behavior: is it the mutation or the background genotype?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16388

29 September 2017

Neural tube defects and abnormal brain development in F52-deficient mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16388

29 September 2017

Generation of mice with a 200-kb amyloid precursor protein gene deletion by Cre recombinase-mediated site-specific recombination in embryonic stem cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16388

29 September 2017

MARCKS deficiency in mice leads to abnormal brain development and perinatal death

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16388

29 September 2017

Targeting learning

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16388

29 September 2017

Genetic and developmental defects of the mouse corpus callosum

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16388

29 September 2017

Tests of genetic allelism between four inbred mouse strains with absent corpus callosum

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16388

29 September 2017

A rapid, sensitive histochemical stain for myelin in frozen brain sections

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16388

29 September 2017

Retarded formation of the hippocampal commissure in embryos from mouse strains lacking a corpus callosum.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16388

3 June 2018

Immunocytochemical demonstration of early appearing astroglial structures that form boundaries and pathways along axon tracts in the fetal brain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16388

3 June 2018

Mice in utero while their mother is lactating suffer higher frequency of deficient corpus callosum.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16388

3 June 2018

Heritable aspects of anomalous myelinated fibre tracts in the forebrain of the laboratory mouse

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16388

3 June 2018

The efficiency of systematic sampling in stereology and its prediction.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16388

3 June 2018

Deficiency of the corpus callosum: incomplete penetrance and substrain differentiation in BALB/c mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16388

3 June 2018

Deficient corpus callosum in hybrids between ddN and three other abnormal mouse strains.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16388

3 June 2018

Prenatal formation of the normal mouse corpus callosum: a quantitative study with carbocyanine dyes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16388

3 June 2018

The fibers which course within the Probst's longitudinal bundle seen in the brain of a congenitally acallosal mouse: a study with the horseradish peroxidase technique

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.96.8.4656

21 January 2018

Deficiency of corpus callosum varies with strain and supplier of the mice.

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.96.8.4656

21 January 2018

Genetically modified mice and cognition

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.96.8.4656

21 January 2018

Hypersensitivity to seizures in beta-amyloid precursor protein deficient mice

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.96.8.4656

21 January 2018

Axonal guidance during development of the great cerebral commissures: descriptive and experimental studies, in vivo, on the role of preformed glial pathways.

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.96.8.4656

21 January 2018

Mutation of the Emx-1 homeobox gene disrupts the corpus callosum

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.96.8.4656

21 January 2018

Mutant Mice and Neuroscience: Recommendations Concerning Genetic Background

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.96.8.4656

21 January 2018

Sex and species differences in mouse and rat forebrain commissures depend on the method of adjusting for brain size

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16388

27 November 2018

Inheritance of retarded forebrain commissure development in fetal mice: results from classical crosses and recombinant inbred strains

1 reference

https://pubmed.ncbi.nlm.nih.gov/10200318

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cortical axon trajectories and growth cone morphologies in fetuses of acallosal mouse strains

1 reference

https://pubmed.ncbi.nlm.nih.gov/10200318

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new hybrid mouse model for agenesis of the corpus callosum

1 reference

https://pubmed.ncbi.nlm.nih.gov/10200318

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mode of inheritance of deficient corpus callosum in mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/10200318

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1073/PNAS.96.8.4656

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1999PNAS...96.4656M

0 references

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PMC publication ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PubMed publication ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

ResearchGate publication ID

0 references

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