3D-FISH analysis reveals chromatid cohesion defect during interphase in Roberts syndrome. - Test2 - elhamkhani - TriplyDB

3D-FISH analysis reveals chromatid cohesion defect during interphase in Roberts syndrome.

3D-FISH analysis reveals chromatid cohesion defect during interphase in Roberts syndrome.

http://www.wikidata.org/entity/Q34340223

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Ribosomopathies: Global process, tissue specific defects Fluorescence In situ Hybridization: Cell-Based Genetic Diagnostic and Research Applications Thrombocytopenia absent radius syndrome with Tetralogy of Fallot: a rare association.Investigating the Interplay between Sister Chromatid Cohesion and Homolog Pairing in Drosophila Nuclei Zebrafish as a Model to Study Cohesin and Cohesinopathies.

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3D-FISH analysis reveals chromatid cohesion defect during interphase in Roberts syndrome.

http://www.wikidata.org/entity/Q34340223

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2014 nî lūn-bûn

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2014 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

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2014 թվականի սեպտեմբերին հրատարակված գիտական հոդված

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年论文

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3D-FISH analysis reveals chromatid cohesion defect during interphase in Roberts syndrome.

@ast

3D-FISH analysis reveals chromatid cohesion defect during interphase in Roberts syndrome.

@en

3D-FISH analysis reveals chromatid cohesion defect during interphase in Roberts syndrome.

@nl

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label

3D-FISH analysis reveals chromatid cohesion defect during interphase in Roberts syndrome.

@ast

3D-FISH analysis reveals chromatid cohesion defect during interphase in Roberts syndrome.

@en

3D-FISH analysis reveals chromatid cohesion defect during interphase in Roberts syndrome.

@nl

prefLabel

3D-FISH analysis reveals chromatid cohesion defect during interphase in Roberts syndrome.

@ast

3D-FISH analysis reveals chromatid cohesion defect during interphase in Roberts syndrome.

@en

3D-FISH analysis reveals chromatid cohesion defect during interphase in Roberts syndrome.

@nl

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Molecular Cytogenetics

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3D-FISH analysis reveals chromatid cohesion defect during interphase in Roberts syndrome.

@en

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Anne-Claude Tabet

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Benedicte Gerard

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Brigitte Benzacken

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Camille Lebugle

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Celine Dupont

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Daniel Smiljkovski

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Dominique Le Tessier

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Emmanuel Spaggiari

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Fabien Guimiot

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Jean-Michel Dupont

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P2860

Three-dimensional maps of all chromosomes in human male fibroblast nuclei and prometaphase rosettes.

Inactivating mutations in ESCO2 cause SC phocomelia and Roberts syndrome: no phenotype-genotype correlation.

A handcuff model for the cohesin complex

Cohesin is dispensable for centromere cohesion in human cells

Movement of the X chromosome in epilepsy

The non-redundant function of cohesin acetyltransferase Esco2: some answers and new questions.

Cohesin mediates transcriptional insulation by CCCTC-binding factor

Chromosome territories.

Differences in the localization and morphology of chromosomes in the human nucleus.

A zebrafish model of Roberts syndrome reveals that Esco2 depletion interferes with development by disrupting the cell cycle

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