A mutation in Af4 is predicted to cause cerebellar ataxia and cataracts in the robotic mouse. (Q48256073)

PubMed publication ID

12629167

10 February 2018

http://europepmc.org/abstract/MED/12629167

title

A mutation in Af4 is predicted to cause cerebellar ataxia and cataracts in the robotic mouse (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6741966&resulttype=core&format=json

12 May 2020

1 reference

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6741966&resulttype=core&format=json

12 May 2020

15

Kay E Davies

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6741966&resulttype=core&format=json

12 May 2020

8

Lucie Vizor

1 reference

12 May 2020

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6741966&resulttype=core&format=json

5

Allyson Potter

1 reference

12 May 2020

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6741966&resulttype=core&format=json

9

Peter Glenister

1 reference

12 May 2020

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6741966&resulttype=core&format=json

Adrian M Isaacs

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6741966&resulttype=core&format=json

12 May 2020

Peter L Oliver

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6741966&resulttype=core&format=json

12 May 2020

Emma L Jones

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6741966&resulttype=core&format=json

12 May 2020

Alexander Jeans

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6741966&resulttype=core&format=json

12 May 2020

Berit H Hovik

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6741966&resulttype=core&format=json

12 May 2020

Patrick M Nolan

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6741966&resulttype=core&format=json

12 May 2020

Ian C Gray

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6741966&resulttype=core&format=json

12 May 2020

Nigel K Spurr

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6741966&resulttype=core&format=json

12 May 2020

Steve D M Brown

13

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6741966&resulttype=core&format=json

12 May 2020

A Jackie Hunter

14

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6741966&resulttype=core&format=json

12 May 2020

language of work or name

English

0 references

publication date

1 March 2003

1 reference

PubMed publication ID

12629167

10 February 2018

http://europepmc.org/abstract/MED/12629167

published in

Journal of Neuroscience

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6741966&resulttype=core&format=json

12 May 2020

volume

23

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6741966&resulttype=core&format=json

12 May 2020

issue

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6741966&resulttype=core&format=json

12 May 2020

page(s)

1631-1637

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6741966&resulttype=core&format=json

AF5q31, a newly identified AF4-related gene, is fused to MLL in infant acute lymphoblastic leukemia with ins(5;11)(q31;q13q23)

12 May 2020

cites work

1 reference

12 December 2020

Aberrant protein deposition and neurological disease

1 reference

12 December 2020

Insights from mouse models into the molecular basis of neurodegeneration

1 reference

12 December 2020

Altered lymphoid development in mice deficient for the mAF4 proto-oncogene

1 reference

12 December 2020

A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse

1 reference

12 December 2020

Genome-wide, large-scale production of mutant mice by ENU mutagenesis.

1 reference

12 December 2020

Lilliputian: an AF4/FMR2-related protein that controls cell identity and cell growth.

1 reference

12 December 2020

Transcriptional regulation of cytoskeletal functions and segmentation by a novel maternal pair-rule gene, lilliputian

1 reference

12 December 2020

Capitalizing on large-scale mouse mutagenesis screens

1 reference

12 December 2020

Fragile XE-associated familial mental retardation protein 2 (FMR2) acts as a potent transcription activator

1 reference

12 December 2020

Systematic approaches to mouse mutagenesis

1 reference

12 December 2020

Patterned cerebellar Purkinje cell death in a transgenic mouse model of Niemann Pick type A/B disease

1 reference

12 December 2020

Gene-trap mutagenesis: past, present and beyond

1 reference

12 December 2020

Sequence variation and disease in the wake of the draft human genome

1 reference

12 December 2020

The mouse Laf4 gene: exon/intron organization, cDNA sequence, alternative splicing, and expression during central nervous system development.

1 reference

12 December 2020

Reproductive pathology and sperm physiology in acid sphingomyelinase-deficient mice

1 reference

12 December 2020

The t(4;11) chromosome translocation of human acute leukemias fuses the ALL-1 gene, related to Drosophila trithorax, to the AF-4 gene

1 reference

12 December 2020

CD8 surface levels alter the fate of alpha/beta T cell receptor-expressing thymocytes in transgenic mice

1 reference

12 December 2020

The level of CD8 expression can determine the outcome of thymic selection

1 reference

12 December 2020

Niemann-Pick type B disease. Identification of a single codon deletion in the acid sphingomyelinase gene and genotype/phenotype correlations in type A and B patients

1 reference

12 December 2020

New aspects of the pathology of neurodegenerative disorders as revealed by ubiquitin antibodies

1 reference

12 December 2020

Cerebellar cell degeneration in the leaner mutant mouse

1 reference

12 December 2020

Acid sphingomyelinase deficient mice: a model of types A and B Niemann–Pick disease

1 reference

12 December 2020

Acute mixed-lineage leukemia t(4;11)(q21;q23) generates an MLL-AF4 fusion product

1 reference

12 December 2020

Purkinje cell loss from alternating sagittal zones in the cerebellum of leaner mutant mice

1 reference

12 December 2020

Control points in early T-cell development

1 reference

12 December 2020

Molecular analysis of MLL-1/AF4 recombination in infant acute lymphoblastic leukemia

1 reference

12 December 2020

The der(11)-encoded MLL/AF-4 fusion transcript is consistently detected in t(4;11)(q21;q23)-containing acute lymphoblastic leukemia.

1 reference

12 December 2020

Cerebellar degeneration in the Niemann-Pick type C mouse

1 reference

12 December 2020

LAF-4 encodes a lymphoid nuclear protein with transactivation potential that is homologous to AF-4, the gene fused to MLL in t(4;11) leukemias

1 reference

12 December 2020

Domains with transcriptional regulatory activity within the ALL1 and AF4 proteins involved in acute leukemia

1 reference

12 December 2020

Aldolase C/zebrin II and the regionalization of the cerebellum

1 reference

12 December 2020

Identification of FMR2, a novel gene associated with the FRAXE CCG repeat and CpG island

1 reference

12 December 2020

The compartmentalization of the cerebellum

1 reference

12 December 2020

Niemann-Pick C1 disease gene: homology to mediators of cholesterol homeostasis

1 reference

12 December 2020

Exon/intron structure of the human AF‐4 gene, a member of the AF‐4/LAF‐4/FMR‐2 gene family coding for a nuclear protein with structural alterations in acute leukaemia

1 reference

12 December 2020

Gene structure and subcellular localization of FMR2, a member of a new family of putative transcription activators

1 reference

12 December 2020

Behavioral and functional analysis of mouse phenotype: SHIRPA, a proposed protocol for comprehensive phenotype assessment

1 reference

12 December 2020

Cloning and developmental expression of the murine homolog of the acute leukemia proto-oncogene AF4

1 reference

12 December 2020

A method to correct adequately for the change in neuronal size when estimating neuronal numbers after nerve growth factor treatment

1 reference

12 December 2020

Characterization of the testis and epididymis in mouse models of human Tay Sachs and Sandhoff diseases and partial determination of accumulated gangliosides

1 reference

12 December 2020

Identification of novel simple sequence length polymorphisms (SSLPs) in mouse by interspersed repetitive element (IRE)-PCR.

1 reference

12 December 2020

AF4 encodes a ubiquitous protein that in both native and MLL-AF4 fusion types localizes to subnuclear compartments

1 reference

12 December 2020

cDNA cloning, expression and chromosomal localization of the murine AF-4 gene involved in human leukemia

1 reference

12 December 2020

The critical role of chromosome translocations in human leukemias.

1 reference

12 December 2020

10.1523/JNEUROSCI.23-05-01631.2003

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6741966&resulttype=core&format=json

12 May 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6741966&resulttype=core&format=json

12 May 2020

PubMed publication ID

12629167

1 reference