Lista de obras - Thomas Liehr - Dominio Público Uruguay

A New Case of a Complex Small Supernumerary Marker Chromosome: A Der(9)t(7;9)(p22;q22) due to a Maternal Balanced Rearrangement

artículo científico publicado en 2015

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 ⬇️

artículo científico publicado el 4 de agosto de 2010

A rapid method for FISH analysis on interphase nuclei extracted from cryofixed tissues ⬇️

artículo científico publicado el 1 de diciembre de 1996

A study of ten small supernumerary (marker) chromosomes identified by fluorescence in situ hybridization (FISH)

artículo científico publicado el 1 de agosto de 1992

Accumulation of peripheral myelin protein 22 (PMP22) in onion bulbs of nerves biopsied from patients with different subtypes of Charcot-Marie-Tooth disease type 1 ⬇️

artículo científico publicado el 1 de noviembre de 1997

An Insight into the Chromosomal Evolution of Lebiasinidae (Teleostei, Characiformes)

scientific article published on 28 March 2020

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).

artículo científico publicado en 2007

CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NIFA genes

artículo científico publicado en 2016

Chromosomal aberrations in spontaneously aborted products of conception from Ukraine

artículo científico publicado en 2018

Chromosomal evolution in naked catfishes (Bagridae, Siluriformes): A comparative chromosome mapping study

scientific article published in 2014

Chromosomes in a genome-wise order: evidence for metaphase architecture.

artículo científico publicado en 2016

Comparative cytogenetic mapping of rRNA genes among naked catfishes: implications for genomic evolution in the Bagridae family

artículo científico publicado en 2014

Complex chromosomal rearrangements in a secondary acute myeloblastic leukemia after chemotherapy in TRAPS ⬇️

artículo científico publicado el 1 de noviembre de 2003

Comprehensive characterization of evolutionary conserved breakpoints in four New World Monkey karyotypes compared to Chlorocebus aethiops and Homo sapiens

artículo científico publicado en 2015

Cytogenetically visible copy number variations (CG-CNVs) in banding and molecular cytogenetics of human; about heteromorphisms and euchromatic variants

artículo científico publicado en 2016

Cytogenetics of the small-sized fish, Copeina guttata (Characiformes, Lebiasinidae): Novel insights into the karyotype differentiation of the family

scientific article published on 19 December 2019

Cytogenomic characterization of three murine malignant mesothelioma tumor cell lines

scientific article published on 09 September 2020

DNA Copy Number Variations as Markers of Mutagenic Impact

artículo científico publicado en 2019

DNA Methylation Profiling of Uniparental Disomy Subjects Provides a Map of Parental Epigenetic Bias in the Human Genome

artículo científico publicado en 2016

De novo translocation involving two chromosomes in adult prolymphocytic leukemia—A rare case ⬇️

artículo científico publicado el 12 de octubre de 2010

Doxorubicin-Induced Translocation of mtDNA into the Nuclear Genome of Human Lymphocytes Detected Using a Molecular-Cytogenetic Approach

artículo científico publicado en 2020

Enlarged chromosome 13 p‐arm hiding a cryptic partial trisomy 6p22.2‐pter ⬇️

artículo científico publicado el 1 de mayo de 2003

Evolution of the Proto Sex-Chromosome in Solea senegalensis

scientific article published on 15 October 2019

Expression analysis of the PMP22 gene in glioma and osteogenic sarcoma cell lines.

artículo científico publicado en 1999

First detailed reconstruction of the karyotype of Trachypithecus cristatus (Mammalia: Cercopithecidae)

artículo científico publicado en 2013

Giant Sex Chromosomes in Omophoita Species (Coleoptera, Chrysomelidae): Structural and Evolutionary Relationships Revealed by Zoo-FISH and Comparative Genomic Hybridization (CGH)

artículo científico publicado en 2023

High resolution karyotype of Thai crab-eating macaque (Macaca fascicularis)

High resolution karyotype of thai crab-eating macaque (Macaca fascicularis)

Highly Rearranged Karyotypes and Multiple Sex Chromosome Systems in Armored Catfishes from the Genus Harttia (Teleostei, Siluriformes)

artículo científico publicado en 2020

Human adenoma cells are highly susceptible to the genotoxic action of 4-hydroxy-2-nonenal ⬇️

artículo científico publicado el 15 de mayo de 2003

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

artículo científico publicado en 2013

Loss of 9p21 is embedded in a complex but consistent pattern of genomic imbalances in oral squamous cell carcinomas ⬇️

artículo científico publicado el 1 de enero de 2003

Meiotic segregation of complex reciprocal translocations: direct analysis of the spermatozoa of a t(5;13;14) carrier ⬇️

artículo científico publicado el 2 de marzo de 2011

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

artículo científico publicado en 2020

Molecular Cytogenomic Characterization of the Murine Breast Cancer Cell Lines C-127I, EMT6/P and TA3 Hauschka ⬇️

artículo científico publicado en 2020

Molecular cytogenetics reveals complex karyotype in apparent t(8;13) therapy-related acute myeloid leukemia M2 after fibrosarcoma ⬇️

artículo científico publicado el 16 de febrero de 2011

Molecular diagnosis of PMP22 -associated neuropathies using fluorescence in situ hybridization (FISH) on archival peripheral nerve tissue preparations ⬇️

artículo científico publicado el 1 de septiembre de 1997

Multiple Sex Chromosomes and Evolutionary Relationships in Amazonian Catfishes: The Outstanding Model of the Genus Harttia (Siluriformes: Loricariidae)

artículo científico publicado en 2020

New cytogenetically visible copy number variant in region 8q21.2 ⬇️

artículo científico publicado el 5 de enero de 2011

Next generation phenotyping in Emanuel and Pallister Killian Syndrome using computer-aided facial dysmorphology analysis of 2D photos.

artículo científico publicado en 2017

POD-FISH: a new technique for parental origin determination based on copy number variation polymorphism

artículo científico publicado el 1 de enero de 2010

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

artículo científico publicado en 2018

Partial trisomy 9p22 to 9p24.2 in combination with partial monosomy 9pter in a Syrian girl ⬇️

artículo científico publicado el 4 de octubre de 2010

Regional localization of 10 mariner transposon-like ESTs by means of FISH--evidence for a correlation with fragile sites

artículo científico publicado en 2001

Regional localization of rat peripheral myelin protein 22 (Pmp22) gene to Chromosome 10q22 by FISH ⬇️

artículo científico publicado el 1 de julio de 1995

Revisiting the Karyotype Evolution of Neotropical Boid Snakes: A Puzzle Mediated by Chromosomal Fissions

artículo científico publicado en 2020

Revisiting the Karyotypes of Alligators and Caimans (Crocodylia, Alligatoridae) after a Half-Century Delay: Bridging the Gap in the Chromosomal Evolution of Reptiles ⬇️

artículo científico publicado en 2021

Secondary abnormalities involving 1q or 13q and poor outcome in high stage Burkitt leukemia/lymphoma cases with 8q24 rearrangement at diagnosis ⬇️

artículo científico publicado el 5 de enero de 2011

Small Supernumerary Marker Chromosomes in Human Infertility

artículo científico publicado en 2015

Somatic Mosaicism in Cases with Small Supernumerary Marker Chromosomes ⬇️

artículo científico publicado el 1 de septiembre de 2010

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

artículo científico publicado en 2020

The Human Genome Puzzle &#x2014; the Role of Copy Number Variation in Somatic Mosaicism ⬇️

artículo científico publicado el 1 de septiembre de 2010

Trisomy 8 as the sole chromosomal aberration inmyelocytic malignancies: a comprehensive molecular cytogenetic analysis reveals no cryptic aberrations ⬇️

artículo científico publicado el 1 de octubre de 2003

Typical and partial cat eye syndrome: identification of the marker chromosome by FISH

artículo científico publicado el 1 de agosto de 1992

Lista de obras de Thomas Liehr

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 ⬇️

A rapid method for FISH analysis on interphase nuclei extracted from cryofixed tissues ⬇️

A study of ten small supernumerary (marker) chromosomes identified by fluorescence in situ hybridization (FISH)

Accumulation of peripheral myelin protein 22 (PMP22) in onion bulbs of nerves biopsied from patients with different subtypes of Charcot-Marie-Tooth disease type 1 ⬇️

An Insight into the Chromosomal Evolution of Lebiasinidae (Teleostei, Characiformes)

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

Chromosomal aberrations in spontaneously aborted products of conception from Ukraine

Chromosomal evolution in naked catfishes (Bagridae, Siluriformes): A comparative chromosome mapping study

Chromosomes in a genome-wise order: evidence for metaphase architecture.

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 ⬇️

Comprehensive characterization of evolutionary conserved breakpoints in four New World Monkey karyotypes compared to Chlorocebus aethiops and Homo sapiens

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

Cytogenomic characterization of three murine malignant mesothelioma tumor cell lines

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

De novo translocation involving two chromosomes in adult prolymphocytic leukemia—A rare case ⬇️

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 ⬇️

Evolution of the Proto Sex-Chromosome in Solea senegalensis

Expression analysis of the PMP22 gene in glioma and osteogenic sarcoma cell lines.

First detailed reconstruction of the karyotype of Trachypithecus cristatus (Mammalia: Cercopithecidae)

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)

High resolution karyotype of thai crab-eating macaque (Macaca fascicularis)

Highly Rearranged Karyotypes and Multiple Sex Chromosome Systems in Armored Catfishes from the Genus Harttia (Teleostei, Siluriformes)

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 ⬇️

Meiotic segregation of complex reciprocal translocations: direct analysis of the spermatozoa of a t(5;13;14) carrier ⬇️

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

Molecular Cytogenomic Characterization of the Murine Breast Cancer Cell Lines C-127I, EMT6/P and TA3 Hauschka ⬇️

Molecular cytogenetics reveals complex karyotype in apparent t(8;13) therapy-related acute myeloid leukemia M2 after fibrosarcoma ⬇️

Molecular diagnosis of PMP22 -associated neuropathies using fluorescence in situ hybridization (FISH) on archival peripheral nerve tissue preparations ⬇️

Multiple Sex Chromosomes and Evolutionary Relationships in Amazonian Catfishes: The Outstanding Model of the Genus Harttia (Siluriformes: Loricariidae)

New cytogenetically visible copy number variant in region 8q21.2 ⬇️

Next generation phenotyping in Emanuel and Pallister Killian Syndrome using computer-aided facial dysmorphology analysis of 2D photos.

POD-FISH: a new technique for parental origin determination based on copy number variation polymorphism

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 ⬇️

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 ⬇️

Secondary abnormalities involving 1q or 13q and poor outcome in high stage Burkitt leukemia/lymphoma cases with 8q24 rearrangement at diagnosis ⬇️

Small Supernumerary Marker Chromosomes in Human Infertility

Somatic Mosaicism in Cases with Small Supernumerary Marker Chromosomes ⬇️

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

The Human Genome Puzzle &amp;#x2014; the Role of Copy Number Variation in Somatic Mosaicism ⬇️

Trisomy 8 as the sole chromosomal aberration inmyelocytic malignancies: a comprehensive molecular cytogenetic analysis reveals no cryptic aberrations ⬇️

Typical and partial cat eye syndrome: identification of the marker chromosome by FISH

The Human Genome Puzzle — the Role of Copy Number Variation in Somatic Mosaicism ⬇️