Lista de obras - Janine M. LaSalle - Dominio Público Uruguay

15q11.2-13.3 chromatin analysis reveals epigenetic regulation of CHRNA7 with deficiencies in Rett and autism brain.

artículo científico publicado en 2011

A Prader-Willi locus lncRNA cloud modulates diurnal genes and energy expenditure

artículo científico publicado en 2013

A comparison of existing global DNA methylation assays to low-coverage whole-genome bisulfite sequencing for epidemiological studies.

artículo científico publicado en 2017

A genomic point-of-view on environmental factors influencing the human brain methylome ⬇️

artículo científico publicado el 1 de julio de 2011

A meta-analysis of two high-risk prospective cohort studies reveals autism-specific transcriptional changes to chromatin, autoimmune, and environmental response genes in umbilical cord blood

scientific article published on 24 October 2019

A survey of seizures and current treatments in 15q duplication syndrome

artículo científico publicado en 2014

Automated quantitation of cell-mediated HIV type 1 infection of human syncytiotrophoblast cells by fluorescence in situ hybridization and laser scanning cytometry

artículo científico publicado en 2001

Biological activity of recombinant human myelin basic protein

artículo científico publicado en 1993

Characterization of timed changes in hepatic copper concentrations, methionine metabolism, gene expression, and global DNA methylation in the Jackson toxic milk mouse model of Wilson disease.

artículo científico publicado en 2014

Chimeric MicroRNA-1291 Biosynthesized Efficiently in Escherichia coli Is Effective to Reduce Target Gene Expression in Human Carcinoma Cells and Improve Chemosensitivity.

artículo científico publicado en 2015

Chromosome 15q11-13 duplication syndrome brain reveals epigenetic alterations in gene expression not predicted from copy number.

artículo científico publicado en 2008

Clonal heterogeneity at allelic methylation sites diagnostic for Prader–Willi and Angelman syndromes ⬇️

artículo científico publicado el 17 de febrero de 1998

Cord blood DNA methylome in newborns later diagnosed with autism spectrum disorder reflects early dysregulation of neurodevelopmental and X-linked genes

scientific article published on 14 October 2020

Cord blood buffy coat DNA methylation is comparable to whole cord blood methylation.

artículo científico publicado en 2018

Corrigendum: Genome-Wide Analysis of DNA Methylation, Copy Number Variation, and Gene Expression in Monozygotic Twins Discordant for Primary Biliary Cirrhosis

artículo científico publicado en 2014

Cumulative Impact of Polychlorinated Biphenyl and Large Chromosomal Duplications on DNA Methylation, Chromatin, and Expression of Autism Candidate Genes.

scientific article published on December 2016

Dental Pulp Stem Cells Model Early Life and Imprinted DNA Methylation Patterns

artículo científico publicado en 2016

Does HER2/neu expression provide prognostic information in patients with advanced urothelial carcinoma?

artículo científico

Domain organization of allele-specific replication within the GABRB3 gene cluster requires a biparental 15q11-13 contribution

artículo científico publicado en 1995

Early Developmental and Evolutionary Origins of Gene Body DNA Methylation Patterns in Mammalian Placentas

artículo científico publicado en 2015

Early motor phenotype detection in a female mouse model of Rett syndrome is improved by cross-fostering

artículo científico publicado en 2017

Elevated methyl-CpG-binding protein 2 expression is acquired during postnatal human brain development and is correlated with alternative polyadenylation.

artículo científico publicado en 2002

Epigenetic changes of the thioredoxin system in the tx-j mouse model and in patients with Wilson disease

artículo científico publicado en 2018

Epigenetic investigation of variably X chromosome inactivated genes in monozygotic female twins discordant for primary biliary cirrhosis

artículo científico publicado en 2011

Epigenetic layers and players underlying neurodevelopment.

artículo científico publicado en 2013

Epigenetic mechanisms in diurnal cycles of metabolism and neurodevelopment

artículo científico publicado en 2015

Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3.

artículo científico publicado en 2004

Epigenetic regulation of UBE3A and roles in human neurodevelopmental disorders.

artículo científico publicado en 2015

Epigenomic signatures in liver and blood of Wilson disease patients include hypermethylation of liver-specific enhancers

artículo científico publicado en 2019

Epigenomic strategies at the interface of genetic and environmental risk factors for autism

artículo científico publicado en 2013

Erratum: Investigation of modifier genes within copy number variations in Rett syndrome

article

Experience-dependent neuroplasticity of the developing hypothalamus: integrative epigenomic approaches

scientific article published on 10 May 2018

Experience-dependent neuroplasticity of the developing hypothalamus: integrative epigenomic approaches

Expression Changes in Epigenetic Gene Pathways Associated With One-Carbon Nutritional Metabolites in Maternal Blood From Pregnancies Resulting in Autism and Non-Typical Neurodevelopment

artículo científico publicado en 2020

Expression profiling of clonal lymphocyte cell cultures from Rett syndrome patients

artículo científico publicado en 2006

Gender influences monoallelic expression of ATP10A in human brain

artículo científico publicado en 2008

Genome-wide analysis of DNA methylation, copy number variation, and gene expression in monozygotic twins discordant for primary biliary cirrhosis

artículo científico publicado en 2014

How has the study of the human placenta aided our understanding of partially methylated genes?

artículo científico publicado en 2013

Immunologic and neurodevelopmental susceptibilities of autism

artículo científico publicado en 2008

Imprinting regulates mammalian snoRNA-encoding chromatin decondensation and neuronal nucleolar size.

artículo científico publicado en 2009

Integrated epigenomic analyses of neuronal MeCP2 reveal a role for long-range interaction with active genes

artículo científico publicado en 2007

Large-scale methylation domains mark a functional subset of neuronally expressed genes.

artículo científico publicado en 2011

Levels of select PCB and PBDE congeners in human postmortem brain reveal possible environmental involvement in 15q11‐q13 duplication autism spectrum disorder ⬇️

artículo científico publicado el 29 de agosto de 2012

Long-lived epigenetic interactions between perinatal PBDE exposure and Mecp2308 mutation.

artículo científico publicado en 2012

Loss of MeCP2 in the rat models regression, impaired sociability and transcriptional deficits of Rett syndrome.

artículo científico publicado en 2016

MECP2 mutations in Rett syndrome adversely affect lymphocyte growth, but do not affect imprinted gene expression in blood or brain.

artículo científico publicado en 2002

MECP2 promoter methylation and X chromosome inactivation in autism

artículo científico publicado en 2008

Maternal choline modifies fetal liver copper, gene expression, DNA methylation, and neonatal growth in the tx-j mouse model of Wilson disease

artículo científico publicado en 2013

MeCP2 is required for global heterochromatic and nucleolar changes during activity-dependent neuronal maturation.

artículo científico publicado en 2011

MeCP2 regulates activity-dependent transcriptional responses in olfactory sensory neurons

artículo científico publicado en 2014

Methylation and gene expression responses to ethanol feeding and betaine supplementation in the cystathionine beta synthase-deficient mouse

artículo científico publicado en 2014

Mice with an isoform-ablating Mecp2 exon 1 mutation recapitulate the neurologic deficits of Rett syndrome

artículo científico publicado en 2013

Multiple pathways regulate MeCP2 expression in normal brain development and exhibit defects in autism-spectrum disorders

artículo científico publicado en 2004

Neuron-specific impairment of inter-chromosomal pairing and transcription in a novel model of human 15q-duplication syndrome ⬇️

artículo científico publicado el 1 de octubre de 2011

Neuronal chromatin dynamics of imprinting in development and disease

artículo científico publicado en 2011

Paradoxical role of methyl-CpG-binding protein 2 in Rett syndrome.

artículo científico publicado en 2004

Phosphorylation of distinct sites in MeCP2 modifies cofactor associations and the dynamics of transcriptional regulation

artículo científico publicado en 2012

Placenta and fetal brain share a neurodevelopmental disorder DNA methylation profile in a mouse model of prenatal PCB exposure

artículo científico publicado en 2022

Placental methylome analysis from a prospective autism study

artículo científico publicado en 2016

Placental methylome reveals a 22q13.33 brain regulatory gene locus associated with autism

artículo científico publicado en 2022

R-loop formation at Snord116 mediates topotecan inhibition of Ube3a-antisense and allele-specific chromatin decondensation.

artículo científico publicado en 2013

RAB22 and RAB163/mouse BRCA2: proteins that specifically interact with the RAD51 protein

scientific journal article

Reciprocal co-regulation of EGR2 and MECP2 is disrupted in Rett syndrome and autism

artículo científico publicado en 2009

Reduced MeCP2 expression is frequent in autism frontal cortex and correlates with aberrant MECP2 promoter methylation

artículo científico publicado en 2006

Rett syndrome astrocytes are abnormal and spread MeCP2 deficiency through gap junctions

artículo científico publicado en 2009

Rett syndrome: a Rosetta stone for understanding the molecular pathogenesis of autism

artículo científico publicado en 2005

Role of DNMT3B in the regulation of early neural and neural crest specifiers ⬇️

artículo científico publicado el 1 de enero de 2012

Sequence features accurately predict genome-wide MeCP2 binding in vivo.

artículo científico publicado en 2016

Sex disparate gut microbiome and metabolome perturbations precede disease progression in a mouse model of Rett syndrome

artículo científico publicado en 2021

Small-Magnitude Effect Sizes in Epigenetic End Points are Important in Children's Environmental Health Studies: The Children's Environmental Health and Disease Prevention Research Center's Epigenetics Working Group.

artículo científico publicado en 2017

Snord116-dependent diurnal rhythm of DNA methylation in mouse cortex.

artículo científico publicado en 2018

The coexpression of CD45RA and CD45RO isoforms on T cells during the S/G2/M stages of cell cycle.

artículo científico publicado en 1991

The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13

artículo científico publicado en 2010

The human placenta methylome ⬇️

artículo científico publicado el 25 de marzo de 2013

The landscape of DNA methylation amid a perfect storm of autism aetiologies.

artículo científico publicado en 2016

The role of MeCP2 in brain development and neurodevelopmental disorders

artículo científico publicado en 2010

UBE3A-mediated regulation of imprinted genes and epigenome-wide marks in human neurons.

artículo científico publicado en 2017

Whole genome bisulfite sequencing of Down syndrome brain reveals regional DNA hypermethylation and novel disorder insights

artículo científico publicado en 2019

Wilson Disease: Epigenetic effects of choline supplementation on phenotype and clinical course in a mouse model.

artículo científico publicado en 2016

Wilson's Disease: Changes in Methionine Metabolism and Inflammation Affect Global DNA Methylation in Early Liver Disease ⬇️

artículo científico publicado el 10 de enero de 2013

X chromosome gene methylation in peripheral lymphocytes from monozygotic twins discordant for scleroderma.

artículo científico publicado en 2012

X-Chromosome inactivation ratios affect wild-type MeCP2 expression within mosaic Rett syndrome and Mecp2-/+ mouse brain.

artículo científico publicado en 2004

mtDNA depletion-like syndrome in Wilson disease

artículo científico publicado en 2020

Lista de obras de Janine M. LaSalle

15q11.2-13.3 chromatin analysis reveals epigenetic regulation of CHRNA7 with deficiencies in Rett and autism brain.

A Prader-Willi locus lncRNA cloud modulates diurnal genes and energy expenditure

A comparison of existing global DNA methylation assays to low-coverage whole-genome bisulfite sequencing for epidemiological studies.

A genomic point-of-view on environmental factors influencing the human brain methylome ⬇️

A meta-analysis of two high-risk prospective cohort studies reveals autism-specific transcriptional changes to chromatin, autoimmune, and environmental response genes in umbilical cord blood

A survey of seizures and current treatments in 15q duplication syndrome

Automated quantitation of cell-mediated HIV type 1 infection of human syncytiotrophoblast cells by fluorescence in situ hybridization and laser scanning cytometry

Biological activity of recombinant human myelin basic protein

Characterization of timed changes in hepatic copper concentrations, methionine metabolism, gene expression, and global DNA methylation in the Jackson toxic milk mouse model of Wilson disease.

Chimeric MicroRNA-1291 Biosynthesized Efficiently in Escherichia coli Is Effective to Reduce Target Gene Expression in Human Carcinoma Cells and Improve Chemosensitivity.

Chromosome 15q11-13 duplication syndrome brain reveals epigenetic alterations in gene expression not predicted from copy number.

Clonal heterogeneity at allelic methylation sites diagnostic for Prader–Willi and Angelman syndromes ⬇️

Cord blood DNA methylome in newborns later diagnosed with autism spectrum disorder reflects early dysregulation of neurodevelopmental and X-linked genes

Cord blood buffy coat DNA methylation is comparable to whole cord blood methylation.

Corrigendum: Genome-Wide Analysis of DNA Methylation, Copy Number Variation, and Gene Expression in Monozygotic Twins Discordant for Primary Biliary Cirrhosis

Cumulative Impact of Polychlorinated Biphenyl and Large Chromosomal Duplications on DNA Methylation, Chromatin, and Expression of Autism Candidate Genes.

Dental Pulp Stem Cells Model Early Life and Imprinted DNA Methylation Patterns

Does HER2/neu expression provide prognostic information in patients with advanced urothelial carcinoma?

Domain organization of allele-specific replication within the GABRB3 gene cluster requires a biparental 15q11-13 contribution

Early Developmental and Evolutionary Origins of Gene Body DNA Methylation Patterns in Mammalian Placentas

Early motor phenotype detection in a female mouse model of Rett syndrome is improved by cross-fostering

Elevated methyl-CpG-binding protein 2 expression is acquired during postnatal human brain development and is correlated with alternative polyadenylation.

Epigenetic changes of the thioredoxin system in the tx-j mouse model and in patients with Wilson disease

Epigenetic investigation of variably X chromosome inactivated genes in monozygotic female twins discordant for primary biliary cirrhosis

Epigenetic layers and players underlying neurodevelopment.

Epigenetic mechanisms in diurnal cycles of metabolism and neurodevelopment

Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3.

Epigenetic regulation of UBE3A and roles in human neurodevelopmental disorders.

Epigenomic signatures in liver and blood of Wilson disease patients include hypermethylation of liver-specific enhancers

Epigenomic strategies at the interface of genetic and environmental risk factors for autism

Erratum: Investigation of modifier genes within copy number variations in Rett syndrome

Experience-dependent neuroplasticity of the developing hypothalamus: integrative epigenomic approaches

Experience-dependent neuroplasticity of the developing hypothalamus: integrative epigenomic approaches

Expression Changes in Epigenetic Gene Pathways Associated With One-Carbon Nutritional Metabolites in Maternal Blood From Pregnancies Resulting in Autism and Non-Typical Neurodevelopment

Expression profiling of clonal lymphocyte cell cultures from Rett syndrome patients

Gender influences monoallelic expression of ATP10A in human brain

Genome-wide analysis of DNA methylation, copy number variation, and gene expression in monozygotic twins discordant for primary biliary cirrhosis

How has the study of the human placenta aided our understanding of partially methylated genes?

Immunologic and neurodevelopmental susceptibilities of autism

Imprinting regulates mammalian snoRNA-encoding chromatin decondensation and neuronal nucleolar size.

Integrated epigenomic analyses of neuronal MeCP2 reveal a role for long-range interaction with active genes

Large-scale methylation domains mark a functional subset of neuronally expressed genes.

Levels of select PCB and PBDE congeners in human postmortem brain reveal possible environmental involvement in 15q11‐q13 duplication autism spectrum disorder ⬇️

Long-lived epigenetic interactions between perinatal PBDE exposure and Mecp2308 mutation.

Loss of MeCP2 in the rat models regression, impaired sociability and transcriptional deficits of Rett syndrome.

MECP2 mutations in Rett syndrome adversely affect lymphocyte growth, but do not affect imprinted gene expression in blood or brain.

MECP2 promoter methylation and X chromosome inactivation in autism

Maternal choline modifies fetal liver copper, gene expression, DNA methylation, and neonatal growth in the tx-j mouse model of Wilson disease

MeCP2 is required for global heterochromatic and nucleolar changes during activity-dependent neuronal maturation.

MeCP2 regulates activity-dependent transcriptional responses in olfactory sensory neurons

Methylation and gene expression responses to ethanol feeding and betaine supplementation in the cystathionine beta synthase-deficient mouse

Mice with an isoform-ablating Mecp2 exon 1 mutation recapitulate the neurologic deficits of Rett syndrome

Multiple pathways regulate MeCP2 expression in normal brain development and exhibit defects in autism-spectrum disorders

Neuron-specific impairment of inter-chromosomal pairing and transcription in a novel model of human 15q-duplication syndrome ⬇️

Neuronal chromatin dynamics of imprinting in development and disease

Paradoxical role of methyl-CpG-binding protein 2 in Rett syndrome.

Phosphorylation of distinct sites in MeCP2 modifies cofactor associations and the dynamics of transcriptional regulation

Placenta and fetal brain share a neurodevelopmental disorder DNA methylation profile in a mouse model of prenatal PCB exposure

Placental methylome analysis from a prospective autism study

Placental methylome reveals a 22q13.33 brain regulatory gene locus associated with autism

R-loop formation at Snord116 mediates topotecan inhibition of Ube3a-antisense and allele-specific chromatin decondensation.

RAB22 and RAB163/mouse BRCA2: proteins that specifically interact with the RAD51 protein

Reciprocal co-regulation of EGR2 and MECP2 is disrupted in Rett syndrome and autism

Reduced MeCP2 expression is frequent in autism frontal cortex and correlates with aberrant MECP2 promoter methylation

Rett syndrome astrocytes are abnormal and spread MeCP2 deficiency through gap junctions

Rett syndrome: a Rosetta stone for understanding the molecular pathogenesis of autism

Role of DNMT3B in the regulation of early neural and neural crest specifiers ⬇️

Sequence features accurately predict genome-wide MeCP2 binding in vivo.

Sex disparate gut microbiome and metabolome perturbations precede disease progression in a mouse model of Rett syndrome

Small-Magnitude Effect Sizes in Epigenetic End Points are Important in Children's Environmental Health Studies: The Children's Environmental Health and Disease Prevention Research Center's Epigenetics Working Group.

Snord116-dependent diurnal rhythm of DNA methylation in mouse cortex.

The coexpression of CD45RA and CD45RO isoforms on T cells during the S/G2/M stages of cell cycle.

The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13

The human placenta methylome ⬇️

The landscape of DNA methylation amid a perfect storm of autism aetiologies.

The role of MeCP2 in brain development and neurodevelopmental disorders

UBE3A-mediated regulation of imprinted genes and epigenome-wide marks in human neurons.

Whole genome bisulfite sequencing of Down syndrome brain reveals regional DNA hypermethylation and novel disorder insights

Wilson Disease: Epigenetic effects of choline supplementation on phenotype and clinical course in a mouse model.