Lista de obras - Catherine M Abbott - Dominio Público Uruguay

A linkage map for the hybridising toads Bombina bombina and B. variegata (Anura: Discoglossidae).

artículo científico publicado en 2003

Adenosine deaminase,Ada, is in mouse chromosome 2H3, and is not allelic with wasted,wst

artículo científico publicado en 1991

BRK/Sik expression in the gastrointestinal tract and in colon tumors

artículo científico publicado en 1999

Biallelic mutations in the gene encoding eEF1A2 cause seizures and sudden death in F0 mice

artículo científico publicado en 2017

Characterisation of translation elongation factor eEF1B subunit expression in mammalian cells and tissues and co-localisation with eEF1A2.

artículo científico publicado en 2014

Characterization of mouse-hamster somatic cell hybrids by PCR: A panel of mouse-specific primers for each chromosome

artículo científico publicado en 1992

Comparative genomic analysis of genes encoding translation elongation factor 1B(alpha) in human and mouse shows EEF1B1 to be a recent retrotransposition event

artículo científico publicado en 2001

Comparative mapping of 50 human chromosome 9 loci in the laboratory mouse

artículo científico publicado en 1995

Comparative mapping of mouse Chromosome 4 and human Chromosome 9: Lv, Orm, and Hxb are closely linked on mouse Chromosome 4

artículo científico publicado en 1992

Comparative mapping of mouse chromosome 2 and human chromosome 9q: the genes for gelsolin and dopamine beta-hydroxylase map to mouse chromosome 2.

artículo científico publicado en 1992

Deficiency of adenosine deaminase in the wasted mouse

artículo científico publicado en 1986

Development of human chromosome-specific PCR primers for characterization of somatic cell hybrids

article

Dinucleotide repeats in the mouse Hox-4.4 and Hox-4.5 genes on Chromosome 2, and their analysis in the BXD and BXH recombinant inbred strains

article

Distinct functional properties of three human paired-box-protein, PAX8, isoforms generated by alternative splicing in thyroid, kidney and Wilms' tumors

artículo científico publicado en 1995

Eef1a2 promotes cell growth, inhibits apoptosis and activates JAK/STAT and AKT signaling in mouse plasmacytomas

artículo científico publicado en 2010

Efficient and versatile CRISPR engineering of human neurons in culture to model neurological disorders

artículo científico publicado en 2016

Encyclopedia of the mouse genome V. Mouse chromosome 2

scientific article published on 01 January 1996

Erratum

artículo científico publicado en 1993

Eukaryotic elongation factor 1 complex subunits are critical HIV-1 reverse transcription cofactors

artículo científico publicado en 2012

Evolutionary importance of translation elongation factor eEF1A variant switching: eEF1A1 down-regulation in muscle is conserved in Xenopus but is controlled at a post-transcriptional level

artículo científico publicado en 2011

Expression and mapping of the mouse S7/Pmsc2 gene, homolog of an essential mitotic gene in yeast.

artículo científico publicado en 1997

Expression of eEF1A2 is associated with clear cell histology in ovarian carcinomas: overexpression of the gene is not dependent on modifications at the EEF1A2 locus.

artículo científico publicado en 2007

Generation of small mutation in large genomic fragments by homologous recombination: description of the technique and examples of its use.

artículo científico publicado en 1990

Genetic Linkage Analysis of the Ak1, Col5a1, Epb7.2, Fpgs, Grp78, Pbx3, and Notch1 Genes in the Region of Mouse Chromosome 2 Homologous to Human Chromosome 9q

article

Genetic and physical mapping of the mouse Ulnaless locus

artículo científico publicado en 1996

Genetic influences on ovulation of primary oocytes in LT/Sv strain mice

artículo científico publicado en 2004

Genetic studies on a new deficiency gene (PI*Ztun) at the PI locus

artículo científico publicado en 1989

Genomic structure and chromosomal mapping of the murine and human Mbd1, Mbd2, Mbd3, and Mbd4 genes

artículo científico publicado en 1999

Haploinsufficiency for translation elongation factor eEF1A2 in aged mouse muscle and neurons is compatible with normal function.

artículo científico publicado en 2012

Highly homologous eEF1A1 and eEF1A2 exhibit differential post-translational modification with significant enrichment around localised sites of sequence variation

artículo científico publicado en 2013

In vivo characterization of the role of tissue-specific translation elongation factor 1A2 in protein synthesis reveals insights into muscle atrophy

artículo científico publicado en 2013

Isolation and mapping of novel mouse brain cDNA clones containing trinucleotide repeats, and demonstration of novel alleles in recombinant inbred strains.

artículo científico publicado en 1996

Isolation of a Microsatellite That Reveals Paralogy between the Subtelomeric Regions of Mouse Chromosomes 17 and 19: Further Evidence for Telomere–Telomere Exchange in the Mouse

artículo científico publicado en 1998

Linkage Mapping around the Ragged (Ra) and Wasted (wst) Loci on Distal Mouse Chromosome 2

scientific article published on 01 March 1994

Linkage mapping of the Aldo-2, Pax-5, Ambp , and D4H9S3E loci on mouse chromosome 4 in the region of homology with human chromosome 9

scientific article published on 01 December 1993

Mapping in the region of Danforth's short tail and the localization of tail length modifiers.

artículo científico publicado en 1997

Mapping of the structural gene for S-adenosyl homocysteine hydrolase to mouse Chromosome 2, and related sequences to Chromosomes 8 and X

article

Mouse chromosome 2

artículo científico publicado en 1997

Mouse chromosome 2

artículo científico publicado en 1998

Mouse chromosome 2

artículo científico publicado en 1994

Mouse chromosome 2

scientific article published on 01 January 1993

Mouse chromosome 4

artículo científico publicado en 1993

Mouse models of human single gene disorders. I: Nontransgenic mice.

artículo científico publicado en 1992

Multiple molecular dynamics simulation of the isoforms of human translation elongation factor 1A reveals reversible fluctuations between "open" and "closed" conformations and suggests specific for eEF1A1 affinity for Ca2+-calmodulin

artículo científico publicado en 2008

Mutations in Sox18 underlie cardiovascular and hair follicle defects in ragged mice

scientific journal article

Novel de novo EEF1A2 missense mutations causing epilepsy and intellectual disability

artículo científico publicado en 2016

Of mice, men and motor neurons

artículo científico publicado en 2002

PCR as a rapid screening method for transgenic mice

artículo científico publicado en 1988

PRENATAL DIAGNOSIS OF ALPHA-1-ANTITRYPSIN DEFICIENCY USING POLYMERASE CHAIN REACTION

scientific article published on 01 April 1988

Precision Medicine in Epilepsy-The Way Forward?

scientific article published on 01 April 2019

Prenatal diagnosis of alpha-1-antitrypsin deficiency by PCR of linked polymorphisms: A study of 17 cases

scientific article published on 01 April 1992

Progressive loss of motor neuron function in wasted mice: effects of a spontaneous null mutation in the gene for the eEF1 A2 translation factor

artículo científico publicado en 2005

REPORT on the First International Workshop on Chromosome 9 held at Girton College Cambridge, UK, 22?24 March, 1992

scientific article published on 01 July 1992

Recapitulation of the EEF1A2 D252H neurodevelopmental disorder-causing missense mutation in mice reveals a toxic gain of function

artículo científico publicado en 2020

Specific Interaction between eEF1A and HIV RT Is Critical for HIV-1 Reverse Transcription and a Potential Anti-HIV Target

artículo científico publicado en 2015

Structural models of human eEF1A1 and eEF1A2 reveal two distinct surface clusters of sequence variation and potential differences in phosphorylation

artículo científico publicado en 2009

Structure and chromosomal localization of the human 2',3'-cyclic nucleotide 3'-phosphodiesterase gene

artículo científico publicado el 1 de julio de 1992

The assignment of the genes coding for human complement components C6 and C7 to chromosome 5

article

The gene for proliferating cell nuclear antigen (Pcna) maps to mouse Chromosome 2

article

The genes for endothelin 3, vitamin D 24-hydroxylase, and melanocortin 3 receptor map to distal mouse Chromosome 2, in the region of conserved synteny with human Chromosome 20

article

The human homolog of the mouse brown gene maps to the short arm of chromosome 9 and extends the known region of homology with mouse chromosome 4

artículo científico publicado en 1991

The lethal mutation of the mouse wasted (wst) is a deletion that abolishes expression of a tissue-specific isoform of translation elongation factor 1alpha, encoded by the Eef1a2 gene

artículo científico publicado en 1998

The mouse homologue of the human tuberous sclerosis 2 (TSC2) gene maps to chromosome 17, but does not fall within the tw18 or tth20 deletions

article

The reticulocalbin gene maps to the WAGR region in human and to the Small eye Harwell deletion in mouse

artículo científico publicado en 1997

The role of translation elongation factor eEF1 subunits in neurodevelopmental disorders

artículo científico publicado en 2018

The translation elongation factor eEF1A1 couples transcription to translation during heat shock response

artículo científico publicado en 2014

The unexpected roles of eukaryotic translation elongation factors in RNA virus replication and pathogenesis

artículo científico publicado en 2013

The use of irradiation and fusion gene transfer (IFGT) hybrids to isolate DNA clones from human chromosome region 9q33-q34 ⬇️

artículo científico publicado el 1 de septiembre de 1991

Thirteen genes (Cebpb, E2f1, Tcf4, Cyp24, Pck1, Acra4, Edn3, Kcnb1, Mc3r, Ntsr, Cd40, Plcg1 and Rcad) that probably lie in the distal imprinting region of mouse chromosome 2 are not monoallelically expressed

article

Translation elongation factor 1A2 is encoded by one of four closely related eef1a genes and is dispensable for survival in zebrafish

scientific article published on 01 January 2020

Translation elongation factor eEF1A2 is a potential oncoprotein that is overexpressed in two-thirds of breast tumours

artículo científico publicado en 2005

Translation factors: in sickness and in health

artículo científico publicado en 2004

Two opposing effects of mismatch repair on CTG repeat instability in Escherichia coli

artículo científico publicado en 2000

eEF1A demonstrates paralog specific effects on HIV-1 reverse transcription efficiency

article

eEF1A2 and neuronal degeneration

artículo científico publicado en 2009

α1-ANTTTRYPSIN-RELATED GENE (ATR) FOR PRENATAL DIAGNOSIS

article

Lista de obras de Catherine M Abbott

A linkage map for the hybridising toads Bombina bombina and B. variegata (Anura: Discoglossidae).

Adenosine deaminase,Ada, is in mouse chromosome 2H3, and is not allelic with wasted,wst

BRK/Sik expression in the gastrointestinal tract and in colon tumors

Biallelic mutations in the gene encoding eEF1A2 cause seizures and sudden death in F0 mice

Characterisation of translation elongation factor eEF1B subunit expression in mammalian cells and tissues and co-localisation with eEF1A2.

Characterization of mouse-hamster somatic cell hybrids by PCR: A panel of mouse-specific primers for each chromosome

Comparative genomic analysis of genes encoding translation elongation factor 1B(alpha) in human and mouse shows EEF1B1 to be a recent retrotransposition event

Comparative mapping of 50 human chromosome 9 loci in the laboratory mouse

Comparative mapping of mouse Chromosome 4 and human Chromosome 9: Lv, Orm, and Hxb are closely linked on mouse Chromosome 4

Comparative mapping of mouse chromosome 2 and human chromosome 9q: the genes for gelsolin and dopamine beta-hydroxylase map to mouse chromosome 2.

Deficiency of adenosine deaminase in the wasted mouse

Development of human chromosome-specific PCR primers for characterization of somatic cell hybrids

Dinucleotide repeats in the mouse Hox-4.4 and Hox-4.5 genes on Chromosome 2, and their analysis in the BXD and BXH recombinant inbred strains

Distinct functional properties of three human paired-box-protein, PAX8, isoforms generated by alternative splicing in thyroid, kidney and Wilms' tumors

Eef1a2 promotes cell growth, inhibits apoptosis and activates JAK/STAT and AKT signaling in mouse plasmacytomas

Efficient and versatile CRISPR engineering of human neurons in culture to model neurological disorders

Encyclopedia of the mouse genome V. Mouse chromosome 2

Erratum

Eukaryotic elongation factor 1 complex subunits are critical HIV-1 reverse transcription cofactors

Evolutionary importance of translation elongation factor eEF1A variant switching: eEF1A1 down-regulation in muscle is conserved in Xenopus but is controlled at a post-transcriptional level

Expression and mapping of the mouse S7/Pmsc2 gene, homolog of an essential mitotic gene in yeast.

Expression of eEF1A2 is associated with clear cell histology in ovarian carcinomas: overexpression of the gene is not dependent on modifications at the EEF1A2 locus.

Generation of small mutation in large genomic fragments by homologous recombination: description of the technique and examples of its use.

Genetic Linkage Analysis of the Ak1, Col5a1, Epb7.2, Fpgs, Grp78, Pbx3, and Notch1 Genes in the Region of Mouse Chromosome 2 Homologous to Human Chromosome 9q

Genetic and physical mapping of the mouse Ulnaless locus

Genetic influences on ovulation of primary oocytes in LT/Sv strain mice

Genetic studies on a new deficiency gene (PI*Ztun) at the PI locus

Genomic structure and chromosomal mapping of the murine and human Mbd1, Mbd2, Mbd3, and Mbd4 genes

Haploinsufficiency for translation elongation factor eEF1A2 in aged mouse muscle and neurons is compatible with normal function.

Highly homologous eEF1A1 and eEF1A2 exhibit differential post-translational modification with significant enrichment around localised sites of sequence variation

In vivo characterization of the role of tissue-specific translation elongation factor 1A2 in protein synthesis reveals insights into muscle atrophy

Isolation and mapping of novel mouse brain cDNA clones containing trinucleotide repeats, and demonstration of novel alleles in recombinant inbred strains.

Isolation of a Microsatellite That Reveals Paralogy between the Subtelomeric Regions of Mouse Chromosomes 17 and 19: Further Evidence for Telomere–Telomere Exchange in the Mouse

Linkage Mapping around the Ragged (Ra) and Wasted (wst) Loci on Distal Mouse Chromosome 2

Linkage mapping of the Aldo-2, Pax-5, Ambp , and D4H9S3E loci on mouse chromosome 4 in the region of homology with human chromosome 9

Mapping in the region of Danforth's short tail and the localization of tail length modifiers.

Mapping of the structural gene for S-adenosyl homocysteine hydrolase to mouse Chromosome 2, and related sequences to Chromosomes 8 and X

Mouse chromosome 2

Mouse chromosome 2

Mouse chromosome 2

Mouse chromosome 2

Mouse chromosome 4

Mouse models of human single gene disorders. I: Nontransgenic mice.

Multiple molecular dynamics simulation of the isoforms of human translation elongation factor 1A reveals reversible fluctuations between "open" and "closed" conformations and suggests specific for eEF1A1 affinity for Ca2+-calmodulin

Mutations in Sox18 underlie cardiovascular and hair follicle defects in ragged mice

Novel de novo EEF1A2 missense mutations causing epilepsy and intellectual disability

Of mice, men and motor neurons

PCR as a rapid screening method for transgenic mice

PRENATAL DIAGNOSIS OF ALPHA-1-ANTITRYPSIN DEFICIENCY USING POLYMERASE CHAIN REACTION

Precision Medicine in Epilepsy-The Way Forward?

Prenatal diagnosis of alpha-1-antitrypsin deficiency by PCR of linked polymorphisms: A study of 17 cases

Progressive loss of motor neuron function in wasted mice: effects of a spontaneous null mutation in the gene for the eEF1 A2 translation factor

REPORT on the First International Workshop on Chromosome 9 held at Girton College Cambridge, UK, 22?24 March, 1992

Recapitulation of the EEF1A2 D252H neurodevelopmental disorder-causing missense mutation in mice reveals a toxic gain of function

Specific Interaction between eEF1A and HIV RT Is Critical for HIV-1 Reverse Transcription and a Potential Anti-HIV Target

Structural models of human eEF1A1 and eEF1A2 reveal two distinct surface clusters of sequence variation and potential differences in phosphorylation

Structure and chromosomal localization of the human 2',3'-cyclic nucleotide 3'-phosphodiesterase gene

The assignment of the genes coding for human complement components C6 and C7 to chromosome 5

The gene for proliferating cell nuclear antigen (Pcna) maps to mouse Chromosome 2

The genes for endothelin 3, vitamin D 24-hydroxylase, and melanocortin 3 receptor map to distal mouse Chromosome 2, in the region of conserved synteny with human Chromosome 20

The human homolog of the mouse brown gene maps to the short arm of chromosome 9 and extends the known region of homology with mouse chromosome 4

The lethal mutation of the mouse wasted (wst) is a deletion that abolishes expression of a tissue-specific isoform of translation elongation factor 1alpha, encoded by the Eef1a2 gene

The mouse homologue of the human tuberous sclerosis 2 (TSC2) gene maps to chromosome 17, but does not fall within the tw18 or tth20 deletions

The reticulocalbin gene maps to the WAGR region in human and to the Small eye Harwell deletion in mouse

The role of translation elongation factor eEF1 subunits in neurodevelopmental disorders

The translation elongation factor eEF1A1 couples transcription to translation during heat shock response

The unexpected roles of eukaryotic translation elongation factors in RNA virus replication and pathogenesis

The use of irradiation and fusion gene transfer (IFGT) hybrids to isolate DNA clones from human chromosome region 9q33-q34 ⬇️

Thirteen genes (Cebpb, E2f1, Tcf4, Cyp24, Pck1, Acra4, Edn3, Kcnb1, Mc3r, Ntsr, Cd40, Plcg1 and Rcad) that probably lie in the distal imprinting region of mouse chromosome 2 are not monoallelically expressed

Translation elongation factor 1A2 is encoded by one of four closely related eef1a genes and is dispensable for survival in zebrafish

Translation elongation factor eEF1A2 is a potential oncoprotein that is overexpressed in two-thirds of breast tumours

Translation factors: in sickness and in health

Two opposing effects of mismatch repair on CTG repeat instability in Escherichia coli

eEF1A demonstrates paralog specific effects on HIV-1 reverse transcription efficiency

eEF1A2 and neuronal degeneration

α1-ANTTTRYPSIN-RELATED GENE (ATR) FOR PRENATAL DIAGNOSIS