Liehr, Thomas, 1965-....
Liehr, Thomas
Thomas Liehr investigador
VIAF ID: 27804978 (Personal)
Permalink: http://viaf.org/viaf/27804978
Preferred Forms
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- 100 1 _ ‡a Liehr, Thomas
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- 100 1 _ ‡a Liehr, Thomas
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- 100 1 _ ‡a Liehr, Thomas ‡d 1965-
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- 100 1 _ ‡a Liehr, Thomas, ‡d 1965-
- 100 1 _ ‡a Liehr, Thomas, ‡d 1965-....
- 100 0 _ ‡a Thomas Liehr ‡c investigador
4xx's: Alternate Name Forms (6)
5xx's: Related Names (4)
- 551 _ _ ‡a Erlangen ‡4 ortg ‡4 https://d-nb.info/standards/elementset/gnd#placeOfBirth
- 510 2 _ ‡a Friedrich-Schiller-Universität Jena ‡4 affi ‡4 https://d-nb.info/standards/elementset/gnd#affiliation ‡e Affiliation
- 510 2 _ ‡a Institut für Humangenetik und Anthropologie Jena ‡4 affi ‡4 https://d-nb.info/standards/elementset/gnd#affiliation ‡e Affiliation
- 551 _ _ ‡a Jena ‡4 ortw ‡4 https://d-nb.info/standards/elementset/gnd#placeOfActivity
Works
Title | Sources |
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The Amazonian Red Side-Necked Turtle Rhinemys rufipes (Spix, 1824) (Testudines, Chelidae) Has a GSD Sex-Determining Mechanism with an Ancient XY Sex Microchromosome System | |
Attrition of X chromosome inactivation in aged hematopoietic stem cells | |
Auswirkungen ausgewählter REEP1-Mutationen auf das Spleißen von prä-mRNA | |
Benign and pathological chromosomal imbalances microscopic and submicroscopic copy number variations (CNVs) in genetics and counseling | |
Bilateral periventricular nodular heterotopia, severe learning disability, and epilepsy in a male patient with 46,XY,der(19)t(X;19) (q11.1-11.2;p13.3). | |
CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NIFA genes | |
Changes in Telomere Length in Leukocytes and Leukemic Cells after Ultrashort Electron Beam Radiation | |
Chromosomal aberrations in spontaneously aborted products of conception from Ukraine | |
Chromosomes in a genome-wise order: evidence for metaphase architecture. | |
Comparative chromosomal studies in Rhinolophus formosae and R. luctus from China and Vietnam : elevation of R. l. lanosus to species rank | |
Comparative cytogenetic mapping of rRNA genes among naked catfishes: implications for genomic evolution in the Bagridae family | |
Complex chromosomal rearrangements in a secondary acute myeloblastic leukemia after chemotherapy in TRAPS | |
Cytogenetically visible copy number variations (CG-CNVs) in banding and molecular cytogenetics of human; about heteromorphisms and euchromatic variants | |
Cytogenetics of the small-sized fish, Copeina guttata (Characiformes, Lebiasinidae): Novel insights into the karyotype differentiation of the family | |
Cytogenomics of murine melanoma cell lines C57/B1 and B16-F0 | |
DNA Copy Number Variations as Markers of Mutagenic Impact | |
DNA Methylation Profiling of Uniparental Disomy Subjects Provides a Map of Parental Epigenetic Bias in the Human Genome | |
Doxorubicin-Induced Translocation of mtDNA into the Nuclear Genome of Human Lymphocytes Detected Using a Molecular-Cytogenetic Approach | |
Enlarged chromosome 13 p‐arm hiding a cryptic partial trisomy 6p22.2‐pter | |
Evidence for multi-copy Mega-NUMTs in the human genome | |
Evolution of eukaryote genome complexity | |
Evolution of the Proto Sex-Chromosome in Solea senegalensis | |
Evolutionary conserved breakpoints in Old and New World monkeys and their relation to fragile sites observed in Homo sapiens | |
Expression analysis of the PMP22 gene in glioma and osteogenic sarcoma cell lines. | |
First detailed reconstruction of the karyotype of Trachypithecus cristatus (Mammalia: Cercopithecidae) | |
FISH technology | |
Fluorescence in situ hybridization (FISH) : application guide | |
Funktionelle Relevanz von ‚non-homologous chromosomal contacts (NHCCs)‘ | |
Genotyp-Phänotyp-Korrelation bei kleinen überzähligen Marker-Chromosomen des Menschen | |
Giant Sex Chromosomes in Omophoita Species (Coleoptera, Chrysomelidae): Structural and Evolutionary Relationships Revealed by Zoo-FISH and Comparative Genomic Hybridization (CGH) | |
High resolution karyotype of thai crab-eating macaque (Macaca fascicularis) | |
Human adenoma cells are highly susceptible to the genotoxic action of 4-hydroxy-2-nonenal | |
Karyotype and cytogenetic mapping of 9 classes of repetitive DNAs in the genome of the naked catfish Mystus bocourti (Siluriformes, Bagridae). | |
Loss of 9p21 is embedded in a complex but consistent pattern of genomic imbalances in oral squamous cell carcinomas | |
Molecular Cytogenetic Analysis in Freshwater Prawns of the Genus Macrobrachium (Crustacea: Decapoda: Palaemonidae) | |
Molecular cytogenetic characterization of eight small supernumerary marker chromosomes originating from chromosomes 2,4,8,18, and 21 in three patients | |
Molecular Cytogenomic Characterization of the Murine Breast Cancer Cell Lines C-127I, EMT6/P and TA3 Hauschka | |
Multicolor FISH in human cytogenetics | |
Multiple Sex Chromosomes and Evolutionary Relationships in Amazonian Catfishes: The Outstanding Model of the Genus Harttia (Siluriformes: Loricariidae) | |
A New Case of a Complex Small Supernumerary Marker Chromosome: A Der(9)t(7;9)(p22;q22) due to a Maternal Balanced Rearrangement | |
A new cryptic ins(11;1)(q23;q21q31) detected in a t(1;8;11)(q21;p21;q23) in a baby with acute myeloid leukemia FAB AML-M5 | |
New insights into chromomere organization provided by lampbrush chromosome microdissection and high-throughput sequencing | |
Next generation phenotyping in Emanuel and Pallister Killian Syndrome using computer-aided facial dysmorphology analysis of 2D photos. | |
De novo translocation involving two chromosomes in adult prolymphocytic leukemia—A rare case | |
Parental origin of deletions and duplications - about the necessity to check for cryptic inversions. | |
Partial trisomy 9p22 to 9p24.2 in combination with partial monosomy 9pter in a Syrian girl | |
POD-FISH: a new technique for parental origin determination based on copy number variation polymorphism | |
Regional localization of 10 mariner transposon-like ESTs by means of FISH--evidence for a correlation with fragile sites | |
Regional localization of rat peripheral myelin protein 22 (Pmp22) gene to Chromosome 10q22 by FISH | |
Revisiting the Karyotype Evolution of Neotropical Boid Snakes: A Puzzle Mediated by Chromosomal Fissions | |
Revisiting the Karyotypes of Alligators and Caimans (Crocodylia, Alligatoridae) after a Half-Century Delay: Bridging the Gap in the Chromosomal Evolution of Reptiles | |
Satellitome Analysis in the Southern Lapwing ( Vanellus chilensis ) Genome Implications for SatDNA Evolution in Charadriiform Birds | |
Segregation analysis of paracentric inversions in human sperm | |
Small supernumerary marker chromosomes (sSMC) : a guide for human geneticists and clinicians | |
A study of ten small supernumerary | |
Thoughts on the Etiology of Cherubism | |
Trisomy 8 as the sole chromosomal aberration in myelocytic malignancies: a comprehensive molecular cytogenetic analysis reveals no cryptic aberrations | |
Typical and partial cat eye syndrome: identification of the marker chromosome by FISH | |
Uniparental disomy (UPD) in clinical genetics a guide for clinicians and patients | |
Untersuchung der Kopienzahl und des Methylierungsstatus von ITIH5 in zervikalen intraepithelialen Neoplasien an Abstrichmaterial | |
Untersuchungen zur gewebsspezifischen Expression sowie zu möglichen Funktionen des Peripheren-Myelin-Protein-22kDa-(PMP22-)Gens |