Microdissection - a precise method to disclose the parental origin of supernumerary marker chromosomes

Incisional hernia repair in a high-fidelity silicone model for open retro-muscular mesh implantation with preparation of the fatty triangle: validation and educational impact study.

Hernia : the journal of hernias and abdominal wall surgery·2019

Validation and educational impact study of the NANEP high-fidelity simulation model for open preperitoneal mesh repair of umbilical hernia.

Hernia : the journal of hernias and abdominal wall surgery·2019

A randomized trial of safety, pharmacokinetics and pharmacodynamics of concizumab in people with hemophilia A.

Journal of thrombosis and haemostasis : JTH·2018

Clinician's guide to genes associated with Rett-like phenotypes-Investigation of a Danish cohort and review of the literature.

Clinical genetics·2017

Concizumab, an anti-tissue factor pathway inhibitor antibody, induces increased thrombin generation in plasma from haemophilia patients and healthy subjects measured by the thrombin generation assay.

Haemophilia : the official journal of the World Federation of Hemophilia·2017

Structural recovery of the retina in a retinoschisin-deficient mouse after gene replacement therapy by solid lipid nanoparticles.

Biomaterials·2016

Intranuclear arrangement of human chromosome 12 is reflected in metaphase chromosomes as non-random bending.

Annales de genetique·2004

Trisomy 4 associated with double minute chromosomes and MYC amplification in acute myeloblastic leukemia.

Annales de genetique·2004

Large duplication 4q25-q34 with mild clinical effect.

Annales de genetique·2004

A submicroscopic unbalanced subtelomeric translocation t(2p;10q) identified by fluorescence in situ hybridization: fetus with increased nuchal translucency and normal standard karyotype with later growth and developmental delay, rhombencephalosynapsis (RES).

Annales de genetique·2004

Partial trisomy 8q and partial monosomy 18p: a case report.

Annales de genetique·2004

Partial trisomy 18q11.2-->qter due to de novo unbalanced translocation of chromosomes 15 and 18 analyzed by fluorescence in situ hybridization.

Annales de genetique·2004

Chromosome movements in meiotic prophase: regulatory mechanisms and biological roles.

Frontiers in cell and developmental biology·2026

Nuclear diversity in Charophyceae revealed by fluorescence staining and its implications for genome size estimation.

Planta·2026

SANS ankyrin repeats mediate non-classical nuclear import and dictate distinct pathogenic mechanisms.

The FEBS journal·2026

Bone marrow-inspired DLL1-presenting microparticles enhance asymmetric division and maintenance of mouse hematopoietic stem and progenitor cells.

Stem cell reports·2026

Partial trisomy of 1q42.1 and 8q24.3 deletion: a family history.

Revista paulista de pediatria : orgao oficial da Sociedade de Pediatria de Sao Paulo·2026

A Novel Hemizygous CDX4 Missense Variant Identified in a Taiwanese Man with Severe Teratozoospermia.

Medicina (Kaunas, Lithuania)·2026

Related Experiment Videos

Microdissection - a precise method to disclose the parental origin of supernumerary marker chromosomes

Related Concept Videos

Incisional hernia repair in a high-fidelity silicone model for open retro-muscular mesh implantation with preparation of the fatty triangle: validation and educational impact study.

Validation and educational impact study of the NANEP high-fidelity simulation model for open preperitoneal mesh repair of umbilical hernia.

A randomized trial of safety, pharmacokinetics and pharmacodynamics of concizumab in people with hemophilia A.

Clinician's guide to genes associated with Rett-like phenotypes-Investigation of a Danish cohort and review of the literature.

Concizumab, an anti-tissue factor pathway inhibitor antibody, induces increased thrombin generation in plasma from haemophilia patients and healthy subjects measured by the thrombin generation assay.

Structural recovery of the retina in a retinoschisin-deficient mouse after gene replacement therapy by solid lipid nanoparticles.

Intranuclear arrangement of human chromosome 12 is reflected in metaphase chromosomes as non-random bending.

Trisomy 4 associated with double minute chromosomes and MYC amplification in acute myeloblastic leukemia.

Large duplication 4q25-q34 with mild clinical effect.

A submicroscopic unbalanced subtelomeric translocation t(2p;10q) identified by fluorescence in situ hybridization: fetus with increased nuchal translucency and normal standard karyotype with later growth and developmental delay, rhombencephalosynapsis (RES).

Partial trisomy 8q and partial monosomy 18p: a case report.

Partial trisomy 18q11.2-->qter due to de novo unbalanced translocation of chromosomes 15 and 18 analyzed by fluorescence in situ hybridization.

Chromosome movements in meiotic prophase: regulatory mechanisms and biological roles.

Nuclear diversity in Charophyceae revealed by fluorescence staining and its implications for genome size estimation.

SANS ankyrin repeats mediate non-classical nuclear import and dictate distinct pathogenic mechanisms.

Bone marrow-inspired DLL1-presenting microparticles enhance asymmetric division and maintenance of mouse hematopoietic stem and progenitor cells.

Partial trisomy of 1q42.1 and 8q24.3 deletion: a family history.

A Novel Hemizygous CDX4 Missense Variant Identified in a Taiwanese Man with Severe Teratozoospermia.

Related Experiment Videos

Microdissection - a precise method to disclose the parental origin of supernumerary marker chromosomes

Related Concept Videos

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