Lista de obras - Kathrin Saar - Dominio Público Uruguay

1A.05: COMPARISON OF THE WHOLE GENOME SEQUENCE REVEALED GENETICALLY DISTINCT LOCI BETWEEN SHR/IZM AND SHRSP/IZM.

artículo científico publicado en 2015

A Genome-wide Search for Linkage to Asthma22See the Appendix

artículo científico publicado en 1999

A genetic basis for mechanosensory traits in humans

artículo científico publicado en 2012

A trans-acting locus regulates an anti-viral expression network and type 1 diabetes risk

artículo científico publicado en 2010

An eicosanoid protects from statin-induced myopathic changes in primary human cells

Association of AHSG Gene Polymorphisms With Fetuin-A Plasma Levels and Cardiovascular Diseases in the EPIC-Potsdam Study

article

Borna disease virus-induced neuronal degeneration dependent on host genetic background and prevented by soluble factors

artículo científico publicado en 2013

Characterization of the genomic structure and function of regions influencing renin and angiogenesis in the SS rat.

artículo científico publicado en 2011

Combined RNAi and localization for functionally dissecting long noncoding RNAs.

artículo científico publicado en 2012

Combined sequence-based and genetic mapping analysis of complex traits in outbred rats

artículo científico publicado en 2013

Development and application of a DNA microarray-based yeast two-hybrid system

artículo científico publicado en 2013

Diaphragmatic spinal muscular atrophy with respiratory distress is heterogeneous, and one form Is linked to chromosome 11q13-q21.

artículo científico publicado en 1999

Differential gene expression of human chondrocytes cultured under short-term altered gravity conditions during parabolic flight maneuvers.

artículo científico publicado en 2015

Differential gene expression profile and altered cytokine secretion of thyroid cancer cells in space

artículo científico publicado en 2013

Distribution and functional impact of DNA copy number variation in the rat.

artículo científico publicado en 2008

Evidence for involvement of the vitamin D receptor gene in idiopathic short stature via a genome-wide linkage study and subsequent association studies

article

Evidence for linkage of the bladder exstrophy-epispadias complex on chromosome 4q31.21-22 and 19q13.31-41 from a consanguineous Iranian family

artículo científico publicado en 2010

Exploration of a Putative Susceptibility Locus for Idiopathic Generalized Epilepsy on Chromosome 8p12

artículo científico publicado en 2003

Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis maps to chromosome 3q27 and is associated with mutations in the PCLN-1 gene

artículo científico publicado en 2000

Family-based association study of serotonergic candidate genes and attention-deficit/hyperactivity disorder in a German sample.

artículo científico publicado en 2006

Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel beta1 subunit gene SCN1B.

artículo científico publicado en 1998

Fine mapping and single nucleotide polymorphism association results of candidate genes for asthma and related phenotypes.

artículo científico publicado en 2001

Gene localization for an autosomal dominant familial periodic fever to 12p13

artículo científico publicado en 1998

Genome scan for childhood and adolescent obesity in German families

artículo científico publicado en 2003

Genome search for susceptibility loci of common idiopathic generalised epilepsies

artículo científico publicado en 2000

Genome sequencing reveals loci under artificial selection that underlie disease phenotypes in the laboratory rat

artículo científico publicado en 2013

Genome-wide analysis indicates more Asian than Melanesian ancestry of Polynesians

artículo científico publicado en 2008

Genome-wide linkage scan for bladder exstrophy-epispadias complex

artículo científico publicado en 2009

Genomic approach to identify factors that drive the formation of three-dimensional structures by EA.hy926 endothelial cells.

artículo científico publicado en 2013

Gravity‐sensitive signaling drives 3‐dimensional formation of multicellular thyroid cancer spheroids ⬇️

artículo científico publicado el 10 de septiembre de 2012

Hereditary isolated renal magnesium loss maps to chromosome 11q23.

artículo científico publicado en 1999

IL-11 is a crucial determinant of cardiovascular fibrosis.

artículo científico publicado en 2017

Identification of Stim1 as a candidate gene for exaggerated sympathetic response to stress in the stroke-prone spontaneously hypertensive rat.

artículo científico publicado en 2014

Impaired p53-mediated DNA damage response, cell-cycle disturbance and chromosome aberrations in Nijmegen breakage syndrome lymphoblastoid cell lines.

artículo científico publicado en 1999

Impulsivity is a heritable trait in rodents and associated with a novel quantitative trait locus on chromosome 1

artículo científico publicado en 2020

Inflammation-induced acute phase response in skeletal muscle and critical illness myopathy

artículo científico publicado en 2014

Linkage studies exclude the AT-V gene(s) from the translocation breakpoints in an AT-V patient.

artículo científico publicado en 1997

Localisation of a Fanconi anaemia gene to chromosome 9p.

artículo científico publicado en 1998

Localisation of a gene for an autosomal recessive syndrome of macrocephaly, multiple epiphyseal dysplasia, and distinctive facies to chromosome 15q26.

artículo científico publicado en 2001

Low incidence of UPD in spontaneous abortions beyond the 5th gestational week

Molecular-cytogenetic analysis of ancient DNA (aDNA) from preparations from the Meckel collection in Halle (Saale)

artículo científico publicado en 2002

Multiomic analyses uncover immunological signatures in acute and chronic coronary syndromes

artículo científico publicado en 2024

Nibrin, a novel DNA double-strand break repair protein, is mutated in Nijmegen breakage syndrome

artículo científico publicado en 1998

No evidence for a susceptibility locus for idiopathic generalized epilepsy on chromosome 18q21.1.

artículo científico publicado en 2002

No evidence for a susceptibility locus for idiopathic generalized epilepsy on chromosome 5 in families with typical absence seizures

artículo científico publicado en 2002

PTHR1 loss-of-function mutations in familial, nonsyndromic primary failure of tooth eruption

artículo científico publicado en 2008

Primary failure of eruption (PFE)--clinical and molecular genetics analysis.

artículo científico publicado en 2010

Primary failure of eruption (PFE). Clinical and molecular genetics analysis

artículo científico publicado en 2013

Progress and prospects in rat genetics: a community view.

artículo científico publicado en 2008

Protective immune trajectories in early viral containment of non-pneumonic SARS-CoV-2 infection

artículo científico publicado en 2022

RBM20, a gene for hereditary cardiomyopathy, regulates titin splicing

artículo científico publicado en 2012

Renal polyamine excretion, tubular amino acid reabsorption and molecular genetics in cystinuria

article

Retention of lysosomal protein CLN5 in the endoplasmic reticulum causes neuronal ceroid lipofuscinosis in Asian sibship

artículo científico publicado en 2009

Rosuvastatin Can Block Pro-Inflammatory Actions of Transgenic Human C-Reactive Protein Without Reducing its Circulating Levels

artículo científico publicado en 2014

SNP and haplotype mapping for genetic analysis in the rat.

artículo científico publicado en 2008

Short-term weightlessness produced by parabolic flight maneuvers altered gene expression patterns in human endothelial cells.

artículo científico publicado en 2011

Soluble epoxide hydrolase is a susceptibility factor for heart failure in a rat model of human disease

artículo científico publicado en 2008

Splitting schizophrenia: periodic catatonia-susceptibility locus on chromosome 15q15

artículo científico publicado en 2000

Statin-induced myopathic changes in primary human muscle cells and reversal by a prostaglandin F2 alpha analogue

artículo científico publicado en 2020

Systems Genetics Analysis of a Recombinant Inbred Mouse Cell Culture Panel Reveals Wnt Pathway Member Lrp6 as a Regulator of Adult Hippocampal Precursor Cell Proliferation

artículo científico publicado en 2016

The Slavic NBN Founder Mutation: A Role for Reproductive Fitness?

artículo científico publicado en 2016

The gene for the ataxia-telangiectasia variant, Nijmegen breakage syndrome, maps to a 1-cM interval on chromosome 8q21

artículo científico publicado en 1997

The genome sequence of the spontaneously hypertensive rat: Analysis and functional significance

artículo científico publicado en 2010

Thyroid cancer cells in space during the TEXUS-53 sounding rocket mission - The THYROID Project

scientific article published in Scientific Reports

Two genomic regions of chromosomes 1 and 18 explain most of the stroke susceptibility under salt loading in stroke-prone spontaneously hypertensive rat/Izm

artículo científico publicado en 2013

WT1 controls antagonistic FGF and BMP-pSMAD pathways in early renal progenitors

artículo científico publicado en 2014

hKCNN3 which maps to chromosome 1q21 is not the causative gene in periodic catatonia, a familial subtype of schizophrenia

article

Lista de obras de Kathrin Saar

1A.05: COMPARISON OF THE WHOLE GENOME SEQUENCE REVEALED GENETICALLY DISTINCT LOCI BETWEEN SHR/IZM AND SHRSP/IZM.

A Genome-wide Search for Linkage to Asthma22See the Appendix

A genetic basis for mechanosensory traits in humans

A trans-acting locus regulates an anti-viral expression network and type 1 diabetes risk

An eicosanoid protects from statin-induced myopathic changes in primary human cells

Association of AHSG Gene Polymorphisms With Fetuin-A Plasma Levels and Cardiovascular Diseases in the EPIC-Potsdam Study

Borna disease virus-induced neuronal degeneration dependent on host genetic background and prevented by soluble factors

Characterization of the genomic structure and function of regions influencing renin and angiogenesis in the SS rat.

Combined RNAi and localization for functionally dissecting long noncoding RNAs.

Combined sequence-based and genetic mapping analysis of complex traits in outbred rats

Development and application of a DNA microarray-based yeast two-hybrid system

Diaphragmatic spinal muscular atrophy with respiratory distress is heterogeneous, and one form Is linked to chromosome 11q13-q21.

Differential gene expression of human chondrocytes cultured under short-term altered gravity conditions during parabolic flight maneuvers.

Differential gene expression profile and altered cytokine secretion of thyroid cancer cells in space

Distribution and functional impact of DNA copy number variation in the rat.

Evidence for involvement of the vitamin D receptor gene in idiopathic short stature via a genome-wide linkage study and subsequent association studies

Evidence for linkage of the bladder exstrophy-epispadias complex on chromosome 4q31.21-22 and 19q13.31-41 from a consanguineous Iranian family

Exploration of a Putative Susceptibility Locus for Idiopathic Generalized Epilepsy on Chromosome 8p12

Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis maps to chromosome 3q27 and is associated with mutations in the PCLN-1 gene

Family-based association study of serotonergic candidate genes and attention-deficit/hyperactivity disorder in a German sample.

Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel beta1 subunit gene SCN1B.

Fine mapping and single nucleotide polymorphism association results of candidate genes for asthma and related phenotypes.

Gene localization for an autosomal dominant familial periodic fever to 12p13

Genome scan for childhood and adolescent obesity in German families

Genome search for susceptibility loci of common idiopathic generalised epilepsies

Genome sequencing reveals loci under artificial selection that underlie disease phenotypes in the laboratory rat

Genome-wide analysis indicates more Asian than Melanesian ancestry of Polynesians

Genome-wide linkage scan for bladder exstrophy-epispadias complex

Genomic approach to identify factors that drive the formation of three-dimensional structures by EA.hy926 endothelial cells.

Gravity‐sensitive signaling drives 3‐dimensional formation of multicellular thyroid cancer spheroids ⬇️

Hereditary isolated renal magnesium loss maps to chromosome 11q23.

IL-11 is a crucial determinant of cardiovascular fibrosis.

Identification of Stim1 as a candidate gene for exaggerated sympathetic response to stress in the stroke-prone spontaneously hypertensive rat.

Impaired p53-mediated DNA damage response, cell-cycle disturbance and chromosome aberrations in Nijmegen breakage syndrome lymphoblastoid cell lines.

Impulsivity is a heritable trait in rodents and associated with a novel quantitative trait locus on chromosome 1

Inflammation-induced acute phase response in skeletal muscle and critical illness myopathy

Linkage studies exclude the AT-V gene(s) from the translocation breakpoints in an AT-V patient.

Localisation of a Fanconi anaemia gene to chromosome 9p.

Localisation of a gene for an autosomal recessive syndrome of macrocephaly, multiple epiphyseal dysplasia, and distinctive facies to chromosome 15q26.

Low incidence of UPD in spontaneous abortions beyond the 5th gestational week

Molecular-cytogenetic analysis of ancient DNA (aDNA) from preparations from the Meckel collection in Halle (Saale)

Multiomic analyses uncover immunological signatures in acute and chronic coronary syndromes

Nibrin, a novel DNA double-strand break repair protein, is mutated in Nijmegen breakage syndrome

No evidence for a susceptibility locus for idiopathic generalized epilepsy on chromosome 18q21.1.

No evidence for a susceptibility locus for idiopathic generalized epilepsy on chromosome 5 in families with typical absence seizures

PTHR1 loss-of-function mutations in familial, nonsyndromic primary failure of tooth eruption

Primary failure of eruption (PFE)--clinical and molecular genetics analysis.

Primary failure of eruption (PFE). Clinical and molecular genetics analysis

Progress and prospects in rat genetics: a community view.

Protective immune trajectories in early viral containment of non-pneumonic SARS-CoV-2 infection

RBM20, a gene for hereditary cardiomyopathy, regulates titin splicing

Renal polyamine excretion, tubular amino acid reabsorption and molecular genetics in cystinuria

Retention of lysosomal protein CLN5 in the endoplasmic reticulum causes neuronal ceroid lipofuscinosis in Asian sibship

Rosuvastatin Can Block Pro-Inflammatory Actions of Transgenic Human C-Reactive Protein Without Reducing its Circulating Levels

SNP and haplotype mapping for genetic analysis in the rat.

Short-term weightlessness produced by parabolic flight maneuvers altered gene expression patterns in human endothelial cells.

Soluble epoxide hydrolase is a susceptibility factor for heart failure in a rat model of human disease

Splitting schizophrenia: periodic catatonia-susceptibility locus on chromosome 15q15

Statin-induced myopathic changes in primary human muscle cells and reversal by a prostaglandin F2 alpha analogue

Systems Genetics Analysis of a Recombinant Inbred Mouse Cell Culture Panel Reveals Wnt Pathway Member Lrp6 as a Regulator of Adult Hippocampal Precursor Cell Proliferation

The Slavic NBN Founder Mutation: A Role for Reproductive Fitness?

The gene for the ataxia-telangiectasia variant, Nijmegen breakage syndrome, maps to a 1-cM interval on chromosome 8q21

The genome sequence of the spontaneously hypertensive rat: Analysis and functional significance

Thyroid cancer cells in space during the TEXUS-53 sounding rocket mission - The THYROID Project

Two genomic regions of chromosomes 1 and 18 explain most of the stroke susceptibility under salt loading in stroke-prone spontaneously hypertensive rat/Izm

WT1 controls antagonistic FGF and BMP-pSMAD pathways in early renal progenitors

hKCNN3 which maps to chromosome 1q21 is not the causative gene in periodic catatonia, a familial subtype of schizophrenia