(Q45355314)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10407053%20AND%20SRC:MED&resulttype=core&format=json

10 December 2019

title

Cognitive deficits in a genetic mouse model of the most common biochemical cause of human mental retardation (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10407053%20AND%20SRC:MED&resulttype=core&format=json

10 December 2019

author name string

L Zagreda

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10407053%20AND%20SRC:MED&resulttype=core&format=json

10 December 2019

J Goodman

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10407053%20AND%20SRC:MED&resulttype=core&format=json

10 December 2019

D P Druin

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10407053%20AND%20SRC:MED&resulttype=core&format=json

10 December 2019

D McDonald

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10407053%20AND%20SRC:MED&resulttype=core&format=json

10 December 2019

A Diamond

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10407053%20AND%20SRC:MED&resulttype=core&format=json

10 December 2019

language of work or name

English

0 references

publication date

1 July 1999

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10407053%20AND%20SRC:MED&resulttype=core&format=json

10 December 2019

published in

Journal of Neuroscience

1 reference

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10 December 2019

volume

19

1 reference

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10 December 2019

issue

14

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10407053%20AND%20SRC:MED&resulttype=core&format=json

10 December 2019

page(s)

6175-6182

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10407053%20AND%20SRC:MED&resulttype=core&format=json

Mouse models of human phenylketonuria

10 December 2019

cites work

1 reference

12 December 2020

Cloned human phenylalanine hydroxylase gene allows prenatal diagnosis and carrier detection of classical phenylketonuria

1 reference

12 December 2020

Regional mapping of the phenylalanine hydroxylase gene and the phenylketonuria locus in the human genome

1 reference

12 December 2020

Neonatal monoaminergic depletion in mice (Mus musculus) improves performance of a novel odor discrimination task.

1 reference

12 December 2020

Pahhph-5: a mouse mutant deficient in phenylalanine hydroxylase

1 reference

12 December 2020

Reversal and nonreversal shifts in discrimination learning in retardates.

1 reference

12 December 2020

Preliminary report on the effects of diet discontinuation in PKU

1 reference

12 December 2020

Fmr1 knockout mice: a model to study fragile X mental retardation. The Dutch-Belgian Fragile X Consortium

1 reference

12 December 2020

Conservation of hippocampal memory function in rats and humans.

1 reference

12 December 2020

Tight linkage between a splicing mutation and a specific DNA haplotype in phenylketonuria

1 reference

12 December 2020

10.1523/JNEUROSCI.19-14-06175.1999

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10407053%20AND%20SRC:MED&resulttype=core&format=json

10 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10407053%20AND%20SRC:MED&resulttype=core&format=json

10 December 2019

PubMed publication ID

10407053

1 reference