Interphase chromosomal abnormalities and mitotic missegregation of hypomethylated sequences in ICF syndrome cells (Q81692129)

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11 January 2020

title

Interphase chromosomal abnormalities and mitotic missegregation of hypomethylated sequences in ICF syndrome cells (English)

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11 January 2020

author name string

David Gisselsson

1

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11 January 2020

Chunbo Shao

2

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11 January 2020

Cathy M Tuck-Muller

3

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11 January 2020

Suzana Sogorovic

4

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11 January 2020

Eva Pålsson

5

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11 January 2020

Dominique Smeets

6

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Melanie Ehrlich

7

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publication date

27 April 2005

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11 January 2020

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volume

114

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11 January 2020

issue

2

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11 January 2020

page(s)

118-126

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https://scigraph.springernature.com/pub.10.1007/s00412-005-0343-7

11 January 2020

exact match

0 references

cites work

Defective B-cell-negative selection and terminal differentiation in the ICF syndrome.

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12 December 2020

ICF syndrome. Immunodeficiency, chromosomal centromere instability, facial anomalies. Case report and literature review

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12 December 2020

ICF syndrome (immunodeficiency, centromeric instability and facial anomalies): investigation of heterochromatin abnormalities and review of clinical outcome

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12 December 2020

A direct demonstration of somatically paired heterochromatin of human chromosomes

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12 December 2020

Molecular enzymology of the catalytic domains of the Dnmt3a and Dnmt3b DNA methyltransferases

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12 December 2020

Clonal chromosomal aberrations accompanied by strong telomerase activity in immortalization of human B-lymphoblastoid cell lines transformed by Epstein-Barr virus

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12 December 2020

ICF syndrome: a new case and review of the literature

1 reference

12 December 2020

Fragility of the centromeric region of chromosome 1 associated with combined immunodeficiency in siblings. A recessively inherited entity?

1 reference

12 December 2020

An embryonic-like methylation pattern of classical satellite DNA is observed in ICF syndrome

1 reference

12 December 2020

Isolation and characterization of a novel DNA methyltransferase complex linking DNMT3B with components of the mitotic chromosome condensation machinery

1 reference

12 December 2020

DNA methyltransferases Dnmt3a and Dnmt3b are essential for de novo methylation and mammalian development

1 reference

12 December 2020

Whole-genome methylation scan in ICF syndrome: hypomethylation of non-satellite DNA repeats D4Z4 and NBL2.

1 reference

12 December 2020

Measurement of telomere length in haematopoietic cells using in situ hybridization techniques

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12 December 2020

Preferential induction of chromosome 1 multibranched figures and whole-arm deletions in a human pro-B cell line treated with 5-azacytidine or 5-azadeoxycytidine

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12 December 2020

Heterogeneity in telomere length of human chromosomes.

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12 December 2020

Chromosome instability in ICF syndrome: formation of micronuclei from multibranched chromosomes 1 demonstrated by fluorescence in situ hybridization

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12 December 2020

Observations of radiation-induced chromosome fragment loss in live mammalian cells in culture, and its effect on colony-forming ability

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12 December 2020

Interphase cytogenetics of the ICF syndrome

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12 December 2020

The ICF syndrome, a DNA methyltransferase 3B deficiency and immunodeficiency disease

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12 December 2020

Chromosome instability in cancer: how, when, and why?

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Specific induction of uncoiling and recombination by azacytidine in classical satellite-containing constitutive heterochromatin.

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12 December 2020

The DNMT3B DNA methyltransferase gene is mutated in the ICF immunodeficiency syndrome

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12 December 2020

DNA methyltransferase 3B mutations linked to the ICF syndrome cause dysregulation of lymphogenesis genes

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12 December 2020

Non-Hodgkin's lymphoma in pediatric patients with chromosomal breakage syndromes (AT and NBS): experience from the BFM trials

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12 December 2020

Hypersensitivity to radiation-induced non-apoptotic and apoptotic death in cell lines from patients with the ICF chromosome instability syndrome

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12 December 2020

Variable immunodeficiency with abnormal condensation of the heterochromatin of chromosomes 1, 9, and 16

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12 December 2020

Multibranched chromosomes 1, 9, and 16 in a patient with combined IgA and IgE deficiency

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12 December 2020

Telomere dysfunction triggers extensive DNA fragmentation and evolution of complex chromosome abnormalities in human malignant tumors

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12 December 2020

Locus-specific multifluor FISH analysis allows physical characterization of complex chromosome abnormalities in neoplasia

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12 December 2020

Comparison of human mammary epithelial cells immortalized by simian virus 40 T-Antigen or by the telomerase catalytic subunit

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12 December 2020

Immunodeficiency, centromeric heterochromatin instability of chromosomes 1, 9, and 16, and facial anomalies: the ICF syndrome

1 reference

12 December 2020

Genetic variation in ICF syndrome: evidence for genetic heterogeneity

1 reference

12 December 2020

Multibranched chromosomes in the ICF syndrome: immunodeficiency, centromeric instability, and facial anomalies

1 reference

12 December 2020

FISH analysis on spontaneously arising micronuclei in the ICF syndrome.

1 reference

12 December 2020

Telomere-mediated mitotic disturbances in immortalized ovarian epithelial cells reproduce chromosomal losses and breakpoints from ovarian carcinoma

1 reference

12 December 2020

Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene

1 reference

12 December 2020

DNA hypomethylation and unusual chromosome instability in cell lines from ICF syndrome patients

1 reference

12 December 2020

10.1007/S00412-005-0343-7

Identifiers

DOI

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11 January 2020

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