Lista de obras - Simon Foote - Dominio Público Uruguay

A Cav3.2 T-type calcium channel point mutation has splice-variant-specific effects on function and segregates with seizure expression in a polygenic rat model of absence epilepsy

artículo científico publicado en 2009

A flow cytometric assay to quantify invasion of red blood cells by rodent Plasmodium parasites in vivo

artículo científico publicado en 2014

A new standard for the assessment of disease progression in murine cutaneous leishmaniasis

artículo científico publicado en 2000

A novel ENU-mutation in ankyrin-1 disrupts malaria parasite maturation in red blood cells of mice

artículo científico publicado en 2012

A polymorphism in the HLA-DPB1 gene is associated with susceptibility to multiple sclerosis

artículo científico publicado en 2010

Adenosine monophosphate deaminase 3 activation shortens erythrocyte half-life and provides malaria resistance in mice.

artículo científico publicado en 2016

Analysis of extended HLA haplotypes in multiple sclerosis and narcolepsy families confirms a predisposing effect for the class I region in Tasmanian MS patients

artículo científico publicado en 2007

Ankyrin-1 Gene Exhibits Allelic Heterogeneity in Conferring Protection Against Malaria.

artículo científico publicado en 2017

Anticipation in familial hematologic malignancies

article

Apolipoprotein genotype does not influence MS severity, cognition, or brain atrophy

artículo científico publicado en 2009

CTLA-4 and multiple sclerosis: the A49G single nucleotide polymorphism shows no association with multiple sclerosis in a Southern Australian population

article

Common and Low Frequency Variants in MERTK Are Independently Associated with Multiple Sclerosis Susceptibility with Discordant Association Dependent upon HLA-DRB1*15:01 Status.

artículo científico publicado en 2016

Complete amino acid sequence and maturation of the mouse submaxillary gland renin precursor

artículo científico publicado en 1982

Controlling malaria and African trypanosomiasis: the role of the mouse

artículo científico publicado en 2005

Decreases in HCN mRNA expression in the hippocampus after kindling and status epilepticus in adult rats.

artículo científico publicado en 2008

Detecting genome wide haplotype sharing using SNP or microsatellite haplotype data.

artículo científico publicado en 2005

Dissociation of disease susceptibility, inflammation and cytokine profile in lmr1/2 congenic mice infected with Leishmania major

article

Erythrocytic Iron Deficiency Enhances Susceptibility to Plasmodium chabaudi Infection in Mice Carrying a Missense Mutation in Transferrin Receptor 1

artículo científico publicado en 2015

Evidence for a novel glaucoma locus at chromosome 3p21-22

article

Extended haplotype analysis in the HLA complex reveals an increased frequency of the HFE-C282Y mutation in individuals with multiple sclerosis

artículo científico publicado en 2004

Familial focal epilepsy with variable foci mapped to chromosome 22q12: expansion of the phenotypic spectrum

artículo científico publicado en 2012

Fine mapping of Leishmania major susceptibility Locus lmr2 and evidence of a role for Fli1 in disease and wound healing

artículo científico publicado en 2010

Fine mapping of multiple sclerosis susceptibility genes provides evidence of allelic heterogeneity at the IL2RA locus.

artículo científico publicado en 2009

Generating mouse models of retinal disease using ENU mutagenesis.

artículo científico publicado en 2002

Genetic absence epilepsy rats from Strasbourg have increased corticothalamic expression of stargazin

artículo científico publicado en 2008

Genetic dissection of the human leukocyte antigen region by use of haplotypes of Tasmanians with multiple sclerosis

artículo científico publicado en 2002

Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

artículo científico publicado en 2011

Genetics of murine leishmaniasis.

artículo científico publicado en 2005

Genome-wide analysis of chemically induced mutations in mouse in phenotype-driven screens

artículo científico publicado en 2015

Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci

artículo científico publicado en 2011

HLA-DRB1 associations with disease susceptibility and clinical course in Australians with multiple sclerosis.

artículo científico publicado en 2009

Heterogeneity at the HLA-DRB1 allelic variation locus does not influence multiple sclerosis disease severity, brain atrophy or cognition

artículo científico publicado en 2010

Host genetics in malaria: lessons from mouse studies.

artículo científico publicado en 2018

Host resistance to malaria: using mouse models to explore the host response

artículo científico publicado en 2010

Human leukocyte antigen-DR15, low infant sibling exposure and multiple sclerosis: Gene-environment interaction

article

Identification of a prostate cancer susceptibility gene on chromosome 5p13q12 associated with risk of both familial and sporadic disease

artículo científico publicado en 2008

Identifying nineteenth century genealogical links from genotypes

artículo científico publicado en 2005

Identity-by-descent approach to gene localisation in eight individuals affected by keratoconus from north-west Tasmania, Australia.

artículo científico publicado en 2002

Improvements in allelic discrimination of microsatellite markers using denaturing polyacrylamide gel electrophoresis

artículo científico publicado en 2000

In vivo assessment of rodent Plasmodium parasitemia and merozoite invasion by flow cytometry.

artículo científico publicado en 2015

Isolation and regional mapping of 110 chromosome 22 STSs.

artículo científico publicado en 1994

Leishmaniasis host response loci (lmr1–3) modify disease severity through a Th1/Th2-independent pathway

article

Leptin's metabolic and immune functions can be uncoupled at the ligand/receptor interaction level

artículo científico publicado en 2014

Linkage to 10q22 for maximum intraocular pressure and 1p32 for maximum cup-to-disc ratio in an extended primary open-angle glaucoma pedigree

artículo científico publicado en 2005

Mapping of the Plasmodium chabaudi resistance locus char2.

artículo científico publicado en 2006

Mice that are congenic for the char2 locus are susceptible to malaria.

artículo científico publicado en 2002

Multiple genetic loci modify susceptibility to plasmacytoma-related morbidity in E(mu)-v-abl transgenic mice

artículo científico publicado en 2002

Multiple sclerosis susceptibility-associated SNPs do not influence disease severity measures in a cohort of Australian MS patients

artículo científico publicado en 2010

Mutation detection using mass spectrometric separation of tiny oligonucleotide fragments

artículo científico publicado en 2002

New insights into the protective power of platelets in malaria infection

artículo científico publicado en 2013

No maternally inherited diabetes and deafness mutations in a sample of 193 Tasmanian diabetics with glaucoma.

artículo científico publicado en 2007

Novel roles for erythroid Ankyrin-1 revealed through an ENU-induced null mouse mutant

scientific article published on 28 January 2009

On the utility of data from the International HapMap Project for Australian association studies.

artículo científico publicado en 2006

PU.1 is a suppressor of myeloid leukemia, inactivated in mice by gene deletion and mutation of its DNA binding domain.

artículo científico publicado en 2004

Platelet factor 4 and Duffy antigen required for platelet killing of Plasmodium falciparum

artículo científico publicado en 2012

Platelets kill intraerythrocytic malarial parasites and mediate survival to infection

artículo científico publicado en 2009

Replication of KIAA0350, IL2RA, RPL5 and CD58 as multiple sclerosis susceptibility genes in Australians

artículo científico publicado en 2008

SNP mapping and candidate gene sequencing in the class I region of the HLA complex: searching for multiple sclerosis susceptibility genes in Tasmanians

artículo científico publicado en 2007

Stargazin and AMPA receptor membrane expression is increased in the somatosensory cortex of Genetic Absence Epilepsy Rats from Strasbourg

artículo científico publicado en 2011

Structure of the RESA gene of Plasmodium falciparum.

artículo científico publicado en 1986

Targeting the cell stress response of Plasmodium falciparum to overcome artemisinin resistance

artículo científico publicado en 2015

The advantages of dense marker sets for linkage analysis with very large families.

artículo científico publicado en 2007

The influence of host genetics on erythrocytes and malaria infection: is there therapeutic potential?

artículo científico publicado en 2015

The wound repair response controls outcome to cutaneous leishmaniasis.

artículo científico publicado en 2005

Treatment of erythrocytes with the 2-cys peroxiredoxin inhibitor, Conoidin A, prevents the growth of Plasmodium falciparum and enhances parasite sensitivity to chloroquine

artículo científico publicado en 2014

What can Bioinformatics do for Parasitology Research?

scientific article published on 01 September 1998

Wound healing response is a major contributor to the severity of cutaneous leishmaniasis in the ear model of infection

article

Lista de obras de Simon Foote

A Cav3.2 T-type calcium channel point mutation has splice-variant-specific effects on function and segregates with seizure expression in a polygenic rat model of absence epilepsy

A flow cytometric assay to quantify invasion of red blood cells by rodent Plasmodium parasites in vivo

A new standard for the assessment of disease progression in murine cutaneous leishmaniasis

A novel ENU-mutation in ankyrin-1 disrupts malaria parasite maturation in red blood cells of mice

A polymorphism in the HLA-DPB1 gene is associated with susceptibility to multiple sclerosis

Adenosine monophosphate deaminase 3 activation shortens erythrocyte half-life and provides malaria resistance in mice.

Analysis of extended HLA haplotypes in multiple sclerosis and narcolepsy families confirms a predisposing effect for the class I region in Tasmanian MS patients

Ankyrin-1 Gene Exhibits Allelic Heterogeneity in Conferring Protection Against Malaria.

Anticipation in familial hematologic malignancies

Apolipoprotein genotype does not influence MS severity, cognition, or brain atrophy

CTLA-4 and multiple sclerosis: the A49G single nucleotide polymorphism shows no association with multiple sclerosis in a Southern Australian population

Common and Low Frequency Variants in MERTK Are Independently Associated with Multiple Sclerosis Susceptibility with Discordant Association Dependent upon HLA-DRB1*15:01 Status.

Complete amino acid sequence and maturation of the mouse submaxillary gland renin precursor

Controlling malaria and African trypanosomiasis: the role of the mouse

Decreases in HCN mRNA expression in the hippocampus after kindling and status epilepticus in adult rats.

Detecting genome wide haplotype sharing using SNP or microsatellite haplotype data.

Dissociation of disease susceptibility, inflammation and cytokine profile in lmr1/2 congenic mice infected with Leishmania major

Erythrocytic Iron Deficiency Enhances Susceptibility to Plasmodium chabaudi Infection in Mice Carrying a Missense Mutation in Transferrin Receptor 1

Evidence for a novel glaucoma locus at chromosome 3p21-22

Extended haplotype analysis in the HLA complex reveals an increased frequency of the HFE-C282Y mutation in individuals with multiple sclerosis

Familial focal epilepsy with variable foci mapped to chromosome 22q12: expansion of the phenotypic spectrum

Fine mapping of Leishmania major susceptibility Locus lmr2 and evidence of a role for Fli1 in disease and wound healing

Fine mapping of multiple sclerosis susceptibility genes provides evidence of allelic heterogeneity at the IL2RA locus.

Generating mouse models of retinal disease using ENU mutagenesis.

Genetic absence epilepsy rats from Strasbourg have increased corticothalamic expression of stargazin

Genetic dissection of the human leukocyte antigen region by use of haplotypes of Tasmanians with multiple sclerosis

Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

Genetics of murine leishmaniasis.

Genome-wide analysis of chemically induced mutations in mouse in phenotype-driven screens

Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci

HLA-DRB1 associations with disease susceptibility and clinical course in Australians with multiple sclerosis.

Heterogeneity at the HLA-DRB1 allelic variation locus does not influence multiple sclerosis disease severity, brain atrophy or cognition

Host genetics in malaria: lessons from mouse studies.

Host resistance to malaria: using mouse models to explore the host response

Human leukocyte antigen-DR15, low infant sibling exposure and multiple sclerosis: Gene-environment interaction

Identification of a prostate cancer susceptibility gene on chromosome 5p13q12 associated with risk of both familial and sporadic disease

Identifying nineteenth century genealogical links from genotypes

Identity-by-descent approach to gene localisation in eight individuals affected by keratoconus from north-west Tasmania, Australia.

Improvements in allelic discrimination of microsatellite markers using denaturing polyacrylamide gel electrophoresis

In vivo assessment of rodent Plasmodium parasitemia and merozoite invasion by flow cytometry.

Isolation and regional mapping of 110 chromosome 22 STSs.

Leishmaniasis host response loci (lmr1–3) modify disease severity through a Th1/Th2-independent pathway

Leptin's metabolic and immune functions can be uncoupled at the ligand/receptor interaction level

Linkage to 10q22 for maximum intraocular pressure and 1p32 for maximum cup-to-disc ratio in an extended primary open-angle glaucoma pedigree

Mapping of the Plasmodium chabaudi resistance locus char2.

Mice that are congenic for the char2 locus are susceptible to malaria.

Multiple genetic loci modify susceptibility to plasmacytoma-related morbidity in E(mu)-v-abl transgenic mice

Multiple sclerosis susceptibility-associated SNPs do not influence disease severity measures in a cohort of Australian MS patients

Mutation detection using mass spectrometric separation of tiny oligonucleotide fragments

New insights into the protective power of platelets in malaria infection

No maternally inherited diabetes and deafness mutations in a sample of 193 Tasmanian diabetics with glaucoma.

Novel roles for erythroid Ankyrin-1 revealed through an ENU-induced null mouse mutant

On the utility of data from the International HapMap Project for Australian association studies.

PU.1 is a suppressor of myeloid leukemia, inactivated in mice by gene deletion and mutation of its DNA binding domain.

Platelet factor 4 and Duffy antigen required for platelet killing of Plasmodium falciparum

Platelets kill intraerythrocytic malarial parasites and mediate survival to infection

Replication of KIAA0350, IL2RA, RPL5 and CD58 as multiple sclerosis susceptibility genes in Australians

SNP mapping and candidate gene sequencing in the class I region of the HLA complex: searching for multiple sclerosis susceptibility genes in Tasmanians

Stargazin and AMPA receptor membrane expression is increased in the somatosensory cortex of Genetic Absence Epilepsy Rats from Strasbourg

Structure of the RESA gene of Plasmodium falciparum.

Targeting the cell stress response of Plasmodium falciparum to overcome artemisinin resistance

The advantages of dense marker sets for linkage analysis with very large families.

The influence of host genetics on erythrocytes and malaria infection: is there therapeutic potential?

The wound repair response controls outcome to cutaneous leishmaniasis.

Treatment of erythrocytes with the 2-cys peroxiredoxin inhibitor, Conoidin A, prevents the growth of Plasmodium falciparum and enhances parasite sensitivity to chloroquine

What can Bioinformatics do for Parasitology Research?

Wound healing response is a major contributor to the severity of cutaneous leishmaniasis in the ear model of infection