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Thomas Liehr (1965-)

Biologe

Name	Thomas Liehr
Zeit	1965- (Lebensdaten)
Ort	Erlangen (Geburtsort) Jena (Wirkungsort) Deutschland
Beruf	Biologe (charakteristischer Beruf) Genetiker
Beziehung	Friedrich-Schiller-Universität Jena Institut für Humangenetik und Anthropologie Jena
Weitere Angaben	Fachhumangenetiker; Institut für Humangenetik und Anthropologie Jena
Datensatztyp	Person
GND-Nummer	115661239
Datensatz-ID	115661239
Beteiligt an alle anzeigen Satellite DNAs and the evolution of the multiple X1X2Y sex chromosomes in the wolf fish Hoplias malabaricus (Teleostei; Characiformes) T-bet+ B cells are activated by and control endogenous retroviruses through TLR-dependent mechanisms A maternally derived complex small supernumerary marker chromosome involving chromosomes 8 and 14 : case report and review of the literature Changes in Telomere Length in Leukocytes and Leukemic Cells after Ultrashort Electron Beam Radiation DNA Damage in Moderate and Severe COVID-19 Cases: Relation to Demographic, Clinical, and Laboratory Parameters Satellitome Analysis in the Southern Lapwing ( Vanellus chilensis ) Genome : Implications for SatDNA Evolution in Charadriiform Birds Thoughts on the Etiology of Cherubism Homeology of sex chromosomes in Amazonian Harttia armored catfishes supports the X-fission hypothesis for the X1X2Y sex chromosome system origin Funktionelle Relevanz von ‚non-homologous chromosomal contacts (NHCCs)‘ Small supernumerary marker chromosomes derived from human chromosome 11 Clinical characterization of 72 patients with del(22)(q11.2q11.2) from different ethnic backgrounds Recommendations for whole genome sequencing in diagnostics for rare diseases Untersuchung der Kopienzahl und des Methylierungsstatus von ITIH5 in zervikalen intraepithelialen Neoplasien an Abstrichmaterial Against the mainstream: exceptional evolutionary stability of ZW sex chromosomes across the fish families Triportheidae and Gasteropelecidae (Teleostei: Characiformes) Correction to: The association of three DNA repair genes polymorphisms on the frequency of chromosomal alterations detected by fluorescence in situ hybridization About classical molecular genetics, cytogenetic and molecular cytogenetic data not considered by Genome Reference Consortium and thus not included in genome browsers like UCSC, Ensembl or NCBI Small supernumerary marker chromosomes derived from chromosome 14 and/or 22 Cytogenomic characteristics of murine breast cancer cell line JC International System for Human Cytogenetic or Cytogenomic Nomenclature (ISCN): Some Thoughts Molecular Cytogenetic Characterization of the Murine Melanoma Cell Lines S91 Clone M3 and B16-F1 with Variant B16-4A5 Low-Level Trisomy 14 Mosaicism: A Carrier of an Isochromosome 14 and a Supernumerary Marker Chromosome 14 Attrition of X chromosome inactivation in aged hematopoietic stem cells Evidence for multi-copy Mega-NUMTs in the human genome Evolution of eukaryote genome complexity Cytogenomic characterization of three murine malignant mesothelioma tumor cell lines Auswirkungen ausgewählter REEP1-Mutationen auf das Spleißen von prä-mRNA Molecular Cytogenetic Analysis in Freshwater Prawns of the Genus Macrobrachium (Crustacea: Decapoda: Palaemonidae) New insights into chromomere organization provided by lampbrush chromosome microdissection and high-throughput sequencing Parental origin of deletions and duplications – about the necessity to check for cryptic inversions Fluorescence In Situ Hybridization (FISH) : Application Guide Benzene poisoning, clinical and blood abnormalities in two Brazilian female gas station attendants: two case reports Analysis and detection of cryptic chromosomal aberrations in chronic lymphocytic leukemia Fluorescence in situ hybridization (FISH) : application guide Fluorescence In Situ Hybridization (FISH) : Application Guide Microdissection of lampbrush chromosomes as an approach for generation of locus-specific FISH-probes and samples for high-throughput sequencing Analysis and detection of cryptic and complex chromosomal aberrations in acute leukemia Evolutionary conserved breakpoints in Old and New World monkeys and their relation to fragile sites observed in Homo sapiens Uniparental disomy (UPD) in clinical genetics : a guide for clinicians and patients Uniparental Disomy (UPD) in Clinical Genetics : A Guide for Clinicians and Patients Karyotype and cytogenetic mapping of 9 classes of repetitive DNAs in the genome of the naked catfish Mystus bocourti (Siluriformes, Bagridae) Complex small supernumerary marker chromosomes – an update Heteromorphic variants of chromosome 9 Small supernumerary marker chromosomes (sSMC) : a guide for human geneticists and clinicians Small Supernumerary Marker Chromosomes (sSMC) : A Guide for Human Geneticists and Clinicians Fluorescence In Situ Hybridization (FISH) — Application Guide Fluorescence in situ hybridization (FISH) : application guide Multicolor FISH in human cytogenetics : 32 tables Genotyp-Phänotyp-Korrelation bei kleinen überzähligen Marker-Chromosomen des Menschen Untersuchungen zur gewebsspezifischen Expression sowie zu möglichen Funktionen des Peripheren-Myelin-Protein-22kDa-(PMP22-)Gens

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Katalog der Deutschen Nationalbibliothek

Thomas Liehr (1965-)

Satellite DNAs and the evolution of the multiple X1X2Y sex chromosomes in the wolf fish Hoplias malabaricus (Teleostei; Characiformes)

T-bet+ B cells are activated by and control endogenous retroviruses through TLR-dependent mechanisms

A maternally derived complex small supernumerary marker chromosome involving chromosomes 8 and 14 : case report and review of the literature

Changes in Telomere Length in Leukocytes and Leukemic Cells after Ultrashort Electron Beam Radiation

DNA Damage in Moderate and Severe COVID-19 Cases: Relation to Demographic, Clinical, and Laboratory Parameters

Satellitome Analysis in the Southern Lapwing ( Vanellus chilensis ) Genome : Implications for SatDNA Evolution in Charadriiform Birds

Thoughts on the Etiology of Cherubism

Homeology of sex chromosomes in Amazonian Harttia armored catfishes supports the X-fission hypothesis for the X1X2Y sex chromosome system origin

Funktionelle Relevanz von ‚non-homologous chromosomal contacts (NHCCs)‘

Small supernumerary marker chromosomes derived from human chromosome 11

Clinical characterization of 72 patients with del(22)(q11.2q11.2) from different ethnic backgrounds

Recommendations for whole genome sequencing in diagnostics for rare diseases

Untersuchung der Kopienzahl und des Methylierungsstatus von ITIH5 in zervikalen intraepithelialen Neoplasien an Abstrichmaterial

Against the mainstream: exceptional evolutionary stability of ZW sex chromosomes across the fish families Triportheidae and Gasteropelecidae (Teleostei: Characiformes)

Correction to: The association of three DNA repair genes polymorphisms on the frequency of chromosomal alterations detected by fluorescence in situ hybridization

About classical molecular genetics, cytogenetic and molecular cytogenetic data not considered by Genome Reference Consortium and thus not included in genome browsers like UCSC, Ensembl or NCBI

Small supernumerary marker chromosomes derived from chromosome 14 and/or 22

Cytogenomic characteristics of murine breast cancer cell line JC

International System for Human Cytogenetic or Cytogenomic Nomenclature (ISCN): Some Thoughts

Molecular Cytogenetic Characterization of the Murine Melanoma Cell Lines S91 Clone M3 and B16-F1 with Variant B16-4A5

Low-Level Trisomy 14 Mosaicism: A Carrier of an Isochromosome 14 and a Supernumerary Marker Chromosome 14

Attrition of X chromosome inactivation in aged hematopoietic stem cells

Evidence for multi-copy Mega-NUMTs in the human genome

Evolution of eukaryote genome complexity

Cytogenomic characterization of three murine malignant mesothelioma tumor cell lines

Auswirkungen ausgewählter REEP1-Mutationen auf das Spleißen von prä-mRNA

Molecular Cytogenetic Analysis in Freshwater Prawns of the Genus Macrobrachium (Crustacea: Decapoda: Palaemonidae)

New insights into chromomere organization provided by lampbrush chromosome microdissection and high-throughput sequencing

Parental origin of deletions and duplications – about the necessity to check for cryptic inversions

Fluorescence In Situ Hybridization (FISH) : Application Guide

Benzene poisoning, clinical and blood abnormalities in two Brazilian female gas station attendants: two case reports

Analysis and detection of cryptic chromosomal aberrations in chronic lymphocytic leukemia

Fluorescence in situ hybridization (FISH) : application guide

Fluorescence In Situ Hybridization (FISH) : Application Guide

Microdissection of lampbrush chromosomes as an approach for generation of locus-specific FISH-probes and samples for high-throughput sequencing

Analysis and detection of cryptic and complex chromosomal aberrations in acute leukemia

Evolutionary conserved breakpoints in Old and New World monkeys and their relation to fragile sites observed in Homo sapiens

Uniparental disomy (UPD) in clinical genetics : a guide for clinicians and patients

Uniparental Disomy (UPD) in Clinical Genetics : A Guide for Clinicians and Patients

Karyotype and cytogenetic mapping of 9 classes of repetitive DNAs in the genome of the naked catfish Mystus bocourti (Siluriformes, Bagridae)

Complex small supernumerary marker chromosomes – an update

Heteromorphic variants of chromosome 9

Small supernumerary marker chromosomes (sSMC) : a guide for human geneticists and clinicians

Small Supernumerary Marker Chromosomes (sSMC) : A Guide for Human Geneticists and Clinicians

Fluorescence In Situ Hybridization (FISH) — Application Guide

Fluorescence in situ hybridization (FISH) : application guide

Multicolor FISH in human cytogenetics : 32 tables

Genotyp-Phänotyp-Korrelation bei kleinen überzähligen Marker-Chromosomen des Menschen

Untersuchungen zur gewebsspezifischen Expression sowie zu möglichen Funktionen des Peripheren-Myelin-Protein-22kDa-(PMP22-)Gens