(Q41276829)

English

DNA, FISH and complementation studies in ICF syndrome: DNA hypomethylation of repetitive and single copy loci and evidence for a trans acting factor

scientific article published on November 1995

In more languages

default for all languages

No label defined

No description defined

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

29 September 2017

DNA, FISH and complementation studies in ICF syndrome: DNA hypomethylation of repetitive and single copy loci and evidence for a trans acting factor (English)

1 reference

Europe PubMed Central

PubMed publication ID

29 September 2017

Thomas Meitinger

9

1 reference

Europe PubMed Central

PubMed publication ID

29 September 2017

author name string

S Schuffenhauer

1

1 reference

Europe PubMed Central

PubMed publication ID

29 September 2017

O Bartsch

2

1 reference

Europe PubMed Central

PubMed publication ID

29 September 2017

M Stumm

3

1 reference

Europe PubMed Central

PubMed publication ID

29 September 2017

T Buchholz

4

1 reference

Europe PubMed Central

PubMed publication ID

29 September 2017

T Petropoulou

5

1 reference

Europe PubMed Central

PubMed publication ID

29 September 2017

S Kraft

6

1 reference

Europe PubMed Central

PubMed publication ID

29 September 2017

B Belohradsky

7

1 reference

Europe PubMed Central

PubMed publication ID

29 September 2017

G K Hinkel

8

1 reference

Europe PubMed Central

PubMed publication ID

29 September 2017

R D Wegner

10

1 reference

Europe PubMed Central

PubMed publication ID

29 September 2017

publication date

1 November 1995

1 reference

Europe PubMed Central

PubMed publication ID

29 September 2017

1 reference

Europe PubMed Central

PubMed publication ID

29 September 2017

96

1 reference

Europe PubMed Central

PubMed publication ID

29 September 2017

5

1 reference

Europe PubMed Central

PubMed publication ID

29 September 2017

562-571

1 reference

Europe PubMed Central

PubMed publication ID

29 September 2017

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8530004

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular diagnosis of the Prader-Willi and Angelman syndromes by detection of parent-of-origin specific DNA methylation in 15q11-13

1 reference

https://pubmed.ncbi.nlm.nih.gov/8530004

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Segmentation of human chromosomes induced by 5-ACR (5-azacytidine)

1 reference

https://pubmed.ncbi.nlm.nih.gov/8530004

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

5-Azacytidine-induced undercondensations in human chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/8530004

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

ICF syndrome: a new case and review of the literature

1 reference

https://pubmed.ncbi.nlm.nih.gov/8530004

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8530004

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8530004

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Monoallelic expression of the human H19 gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/8530004

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cloning of human satellite III DNA: different components are on different chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/8530004

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA methylation and cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/8530004

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abnormal methylation pattern in constitutive and facultative (X inactive chromosome) heterochromatin of ICF patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/8530004

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Simple repeated sequences in human satellite DNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/8530004

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Centromeric heterochromatin instability of chromosomes 1, 9, and 16 in variable immunodeficiency syndrome--a virus-induced phenomenon?

1 reference

https://pubmed.ncbi.nlm.nih.gov/8530004

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Somatic generation of antibody diversity

1 reference

https://pubmed.ncbi.nlm.nih.gov/8530004

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A simplified protocol for fluorescence in situ hybridization with repetitive DNA probes and its use in clinical cytogenetics

1 reference

https://pubmed.ncbi.nlm.nih.gov/8530004

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mapping of Xp21 translocation breakpoints in and around the DMD gene by pulsed field gel electrophoresis

1 reference

https://pubmed.ncbi.nlm.nih.gov/8530004

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Methylation of integrated adenovirus type 12 DNA sequences in transformed cells is inversely correlated with viral gene expression

1 reference

https://pubmed.ncbi.nlm.nih.gov/8530004

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

1 reference

https://pubmed.ncbi.nlm.nih.gov/8530004

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene dosage and complementation analysis of ataxia telangiectasia lymphoblastoid cell lines assayed by induced chromosome aberrations.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8530004

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8530004

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA methylation and gene expression

1 reference

https://pubmed.ncbi.nlm.nih.gov/8530004

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genomic imprinting and uniparental disomy in Angelman and Prader-Willi syndromes: a review

1 reference

https://pubmed.ncbi.nlm.nih.gov/8530004

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Imprinting of human H19: allele-specific CpG methylation, loss of the active allele in Wilms tumor, and potential for somatic allele switching

1 reference

https://pubmed.ncbi.nlm.nih.gov/8530004

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human genome organization: Alu, LINES, and the molecular structure of metaphase chromosome bands

1 reference

https://pubmed.ncbi.nlm.nih.gov/8530004

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

5-Methylcytosine localised in mammalian constitutive heterochromatin.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8530004

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A DNA methylation imprint, determined by the sex of the parent, distinguishes the Angelman and Prader-Willi syndromes

1 reference

https://pubmed.ncbi.nlm.nih.gov/8530004

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The SMC family: novel motor proteins for chromosome condensation?

1 reference

https://pubmed.ncbi.nlm.nih.gov/8530004

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

ICF syndrome with variable expression in sibs

1 reference

https://pubmed.ncbi.nlm.nih.gov/8530004

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA methylation in the Alu sequences of diploid and haploid primary human cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/8530004

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8530004

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The essentials of DNA methylation

1 reference

https://pubmed.ncbi.nlm.nih.gov/8530004

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8530004

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Methylation patterns at the hypervariable X-chromosome locus DXS255 (M27β): Correlation with X-inactivation status

1 reference

https://pubmed.ncbi.nlm.nih.gov/8530004

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosomal localization of human satellites 2 and 3 by a FISH method using oligonucleotides as probes

1 reference

https://pubmed.ncbi.nlm.nih.gov/8530004

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human chromosome-specific repetitive DNA sequences: novel markers for genetic analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/8530004

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of a methylation imprint in the Prader-Willi syndrome chromosome region

1 reference

https://pubmed.ncbi.nlm.nih.gov/8530004

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00197412

1 reference

Europe PubMed Central

PubMed publication ID

29 September 2017

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

29 September 2017

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q41276829&oldid=2204435413"