Lista de obras - Luanne L Peters - Dominio Público Uruguay

A mouse TRAPP-related protein is involved in pigmentation

A new mouse mutant for the LDL receptor identified using ENU mutagenesis

artículo científico publicado en 2008

A novel ENU-generated truncation mutation lacking the spectrin-binding and C-terminal regulatory domains of Ank1 models severe hemolytic hereditary spherocytosis

artículo científico publicado en 2010

Absence of erythroblast macrophage protein (Emp) leads to failure of erythroblast nuclear extrusion

scientific journal article

Accessing Data Resources in the Mouse Phenome Database for Genetic Analysis of Murine Life Span and Health Span

artículo científico publicado en 2014

Aging Research Using Mouse Models.

artículo científico publicado en 2015

Aging in inbred strains of mice: study design and interim report on median lifespans and circulating IGF1 levels

scientific article published on 09 April 2009

Analysis of novel sph (spherocytosis) alleles in mice reveals allele-specific loss of band 3 and adducin in alpha-spectrin-deficient red cells

artículo científico publicado en 2010

Analysis of the mobilities of band 3 populations associated with ankyrin protein and junctional complexes in intact murine erythrocytes

artículo científico publicado en 2011

Cappuccino, a mouse model of Hermansky-Pudlak syndrome, encodes a novel protein that is part of the pallidin-muted complex (BLOC-1)

artículo científico publicado en 2003

Cell-specific mitotic defect and dyserythropoiesis associated with erythroid band 3 deficiency.

artículo científico publicado en 2003

Changes in the expression of splicing factor transcripts and variations in alternative splicing are associated with lifespan in mice and humans.

artículo científico publicado en 2016

Changing patterns in cytoskeletal mRNA expression and protein synthesis during murine erythropoiesis in vivo ⬇️

artículo científico publicado el 1 de julio de 1992

Characterization of glycolytic enzyme interactions with murine erythrocyte membranes in wild-type and membrane protein knockout mice

artículo científico publicado en 2008

Comparative proteomics reveals deficiency of SLC9A1 (sodium/hydrogen exchanger NHE1) in β-adducin null red cells

artículo científico publicado en 2011

Comparison of unrestrained plethysmography and forced oscillation for identifying genetic variability of airway responsiveness in inbred mice

artículo científico publicado en 2010

Critical function for the Ras-GTPase activating protein RASA3 in vertebrate erythropoiesis and megakaryopoiesis

artículo científico publicado en 2012

Differential effects of RASA3 mutations on hematopoiesis are profoundly influenced by genetic background and molecular variant

artículo científico publicado en 2020

Downeast Anemia (dea), a New Mouse Model of Severe Nonspherocytic Hemolytic Anemia Caused by Hexokinase (HKI) Deficiency ⬇️

artículo científico publicado el 1 de septiembre de 2001

Effects of housing density in five inbred strains of mice

artículo científico publicado en 2014

Evidence for a protective role of the Gardos channel against hemolysis in murine spherocytosis

artículo científico publicado en 2005

Genetic Regulation of Female Sexual Maturation and Longevity Through Circulating IGF1

artículo científico publicado en 2015

Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis

artículo científico publicado en 2016

Identification of distal cis-regulatory elements at mouse mitoferrin loci using zebrafish transgenesis.

artículo científico publicado en 2011

Identification of quantitative trait loci that modify the severity of hereditary spherocytosis in wan, a new mouse model of band-3 deficiency

artículo científico publicado en 2003

Impaired synaptic plasticity and learning in mice lacking beta-adducin, an actin-regulating protein

artículo científico publicado en 2005

Implementing large-scale ENU mutagenesis screens in North America

artículo científico publicado en 2004

Invited review: Identifying new mouse models of cardiovascular disease: a review of high-throughput screens of mutagenized and inbred strains

artículo científico publicado en 2003

Iron regulatory protein-1 protects against mitoferrin-1-deficient porphyria

artículo científico publicado en 2014

Iron regulatory protein-1 protects against mitoferrin-1-deficient porphyria

artículo científico publicado en 2014

Lack of protein 4.1G causes altered expression and localization of the cell adhesion molecule nectin-like 4 in testis and can cause male infertility

artículo científico publicado en 2011

Limatin (LIMAB1), an Actin-Binding LIM Protein, Maps to Mouse Chromosome 19 and Human Chromosome 10q25, a Region Frequently Deleted in Human Cancers ⬇️

artículo científico publicado el 1 de diciembre de 1997

Mice as a mammalian model for research on the genetics of aging

artículo científico publicado en 2011

Mitoferrin is essential for erythroid iron assimilation

scientific journal article

Mouse models of USH1C and DFNB18: phenotypic and molecular analyses of two new spontaneous mutations of the Ush1c gene

artículo científico publicado en 2003

N-myristoyltransferase 1 is essential in early mouse development

scientific journal article

Novel method for high-throughput phenotyping of sleep in mice.

artículo científico publicado en 2006

Novel secreted isoform of adhesion molecule ICAM-4: potential regulator of membrane-associated ICAM-4 interactions

scientific journal article

PPAR-α and glucocorticoid receptor synergize to promote erythroid progenitor self-renewal

artículo científico publicado en 2015

Promiscuous DNA-binding of a mutant zinc finger protein corrupts the transcriptome and diminishes cell viability

artículo científico publicado en 2017

Protein 4.2 binds to the carboxyl-terminal EF-hands of erythroid alpha-spectrin in a calcium- and calmodulin-dependent manner

artículo científico publicado en 2009

RASA3 is a critical inhibitor of RAP1-dependent platelet activation

artículo científico publicado en 2015

Reduced pigmentation (rp), a mouse model of Hermansky-Pudlak syndrome, encodes a novel component of the BLOC-1 complex

scientific journal article

Sequence variation at multiple loci influences red cell hemoglobin concentration

artículo científico publicado en 2010

Severe anemia in the Nan mutant mouse caused by sequence-selective disruption of erythroid Kruppel-like factor

artículo científico publicado en 2010

Strain-specific hyperkyphosis and megaesophagus in Add1 null mice

artículo científico publicado en 2012

Strain-specific variations in cation content and transport in mouse erythrocytes

artículo científico publicado en 2013

TMEM14C is required for erythroid mitochondrial heme metabolism

scientific journal article

Targeted deletion of alpha-adducin results in absent beta- and gamma-adducin, compensated hemolytic anemia, and lethal hydrocephalus in mice

scientific journal article

Targeted deletion of betaIII spectrin impairs synaptogenesis and generates ataxic and seizure phenotypes

artículo científico publicado en 2010

Targeted deletion of the gamma-adducin gene (Add3) in mice reveals differences in alpha-adducin interactions in erythroid and nonerythroid cells

artículo científico publicado en 2009

The Actin-Binding Protein α-Adducin Is Required for Maintaining Axon Diameter

artículo científico publicado en 2016

The gene encoding the erythrocyte membrane skeleton protein dematin (Epb4.9) maps to mouse chromosome 14 ⬇️

artículo científico publicado el 10 de abril de 1995

The mouse as a model for human biology: a resource guide for complex trait analysis

artículo científico publicado en 2007

The murine pallid mutation is a platelet storage pool disease associated with the protein 4.2 (pallidin) gene

artículo científico publicado el 1 de septiembre de 1992

The scat mouse model highlights RASA3, a GTPase activating protein, as a key regulator of vertebrate erythropoiesis and megakaryopoiesis

artículo científico publicado en 2012

Tropomodulin 1-null mice have a mild spherocytic elliptocytosis with appearance of tropomodulin 3 in red blood cells and disruption of the membrane skeleton

artículo científico publicado en 2010

alpha- and beta-Adducin polymorphisms affect podocyte proteins and proteinuria in rodents and decline of renal function in human IgA nephropathy

artículo científico publicado en 2009

Lista de obras de Luanne L Peters

A mouse TRAPP-related protein is involved in pigmentation

A new mouse mutant for the LDL receptor identified using ENU mutagenesis

A novel ENU-generated truncation mutation lacking the spectrin-binding and C-terminal regulatory domains of Ank1 models severe hemolytic hereditary spherocytosis

Absence of erythroblast macrophage protein (Emp) leads to failure of erythroblast nuclear extrusion

Accessing Data Resources in the Mouse Phenome Database for Genetic Analysis of Murine Life Span and Health Span

Aging Research Using Mouse Models.

Aging in inbred strains of mice: study design and interim report on median lifespans and circulating IGF1 levels

Analysis of novel sph (spherocytosis) alleles in mice reveals allele-specific loss of band 3 and adducin in alpha-spectrin-deficient red cells

Analysis of the mobilities of band 3 populations associated with ankyrin protein and junctional complexes in intact murine erythrocytes

Cappuccino, a mouse model of Hermansky-Pudlak syndrome, encodes a novel protein that is part of the pallidin-muted complex (BLOC-1)

Cell-specific mitotic defect and dyserythropoiesis associated with erythroid band 3 deficiency.

Changes in the expression of splicing factor transcripts and variations in alternative splicing are associated with lifespan in mice and humans.

Changing patterns in cytoskeletal mRNA expression and protein synthesis during murine erythropoiesis in vivo ⬇️

Characterization of glycolytic enzyme interactions with murine erythrocyte membranes in wild-type and membrane protein knockout mice

Comparative proteomics reveals deficiency of SLC9A1 (sodium/hydrogen exchanger NHE1) in β-adducin null red cells

Comparison of unrestrained plethysmography and forced oscillation for identifying genetic variability of airway responsiveness in inbred mice

Critical function for the Ras-GTPase activating protein RASA3 in vertebrate erythropoiesis and megakaryopoiesis

Differential effects of RASA3 mutations on hematopoiesis are profoundly influenced by genetic background and molecular variant

Downeast Anemia (dea), a New Mouse Model of Severe Nonspherocytic Hemolytic Anemia Caused by Hexokinase (HKI) Deficiency ⬇️

Effects of housing density in five inbred strains of mice

Evidence for a protective role of the Gardos channel against hemolysis in murine spherocytosis

Genetic Regulation of Female Sexual Maturation and Longevity Through Circulating IGF1

Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis

Identification of distal cis-regulatory elements at mouse mitoferrin loci using zebrafish transgenesis.

Identification of quantitative trait loci that modify the severity of hereditary spherocytosis in wan, a new mouse model of band-3 deficiency

Impaired synaptic plasticity and learning in mice lacking beta-adducin, an actin-regulating protein

Implementing large-scale ENU mutagenesis screens in North America

Invited review: Identifying new mouse models of cardiovascular disease: a review of high-throughput screens of mutagenized and inbred strains

Iron regulatory protein-1 protects against mitoferrin-1-deficient porphyria

Iron regulatory protein-1 protects against mitoferrin-1-deficient porphyria

Lack of protein 4.1G causes altered expression and localization of the cell adhesion molecule nectin-like 4 in testis and can cause male infertility

Limatin (LIMAB1), an Actin-Binding LIM Protein, Maps to Mouse Chromosome 19 and Human Chromosome 10q25, a Region Frequently Deleted in Human Cancers ⬇️

Mice as a mammalian model for research on the genetics of aging

Mitoferrin is essential for erythroid iron assimilation

Mouse models of USH1C and DFNB18: phenotypic and molecular analyses of two new spontaneous mutations of the Ush1c gene

N-myristoyltransferase 1 is essential in early mouse development

Novel method for high-throughput phenotyping of sleep in mice.

Novel secreted isoform of adhesion molecule ICAM-4: potential regulator of membrane-associated ICAM-4 interactions

PPAR-α and glucocorticoid receptor synergize to promote erythroid progenitor self-renewal

Promiscuous DNA-binding of a mutant zinc finger protein corrupts the transcriptome and diminishes cell viability

Protein 4.2 binds to the carboxyl-terminal EF-hands of erythroid alpha-spectrin in a calcium- and calmodulin-dependent manner

RASA3 is a critical inhibitor of RAP1-dependent platelet activation

Reduced pigmentation (rp), a mouse model of Hermansky-Pudlak syndrome, encodes a novel component of the BLOC-1 complex

Sequence variation at multiple loci influences red cell hemoglobin concentration

Severe anemia in the Nan mutant mouse caused by sequence-selective disruption of erythroid Kruppel-like factor

Strain-specific hyperkyphosis and megaesophagus in Add1 null mice

Strain-specific variations in cation content and transport in mouse erythrocytes

TMEM14C is required for erythroid mitochondrial heme metabolism

Targeted deletion of alpha-adducin results in absent beta- and gamma-adducin, compensated hemolytic anemia, and lethal hydrocephalus in mice

Targeted deletion of betaIII spectrin impairs synaptogenesis and generates ataxic and seizure phenotypes

Targeted deletion of the gamma-adducin gene (Add3) in mice reveals differences in alpha-adducin interactions in erythroid and nonerythroid cells

The Actin-Binding Protein α-Adducin Is Required for Maintaining Axon Diameter

The gene encoding the erythrocyte membrane skeleton protein dematin (Epb4.9) maps to mouse chromosome 14 ⬇️

The mouse as a model for human biology: a resource guide for complex trait analysis

The murine pallid mutation is a platelet storage pool disease associated with the protein 4.2 (pallidin) gene

The scat mouse model highlights RASA3, a GTPase activating protein, as a key regulator of vertebrate erythropoiesis and megakaryopoiesis

Tropomodulin 1-null mice have a mild spherocytic elliptocytosis with appearance of tropomodulin 3 in red blood cells and disruption of the membrane skeleton

alpha- and beta-Adducin polymorphisms affect podocyte proteins and proteinuria in rodents and decline of renal function in human IgA nephropathy