(Q52547997)

3 May 2018

title

Targeted disruption of Dkc1, the gene mutated in X-linked dyskeratosis congenita, causes embryonic lethality in mice. (English)

1 reference

3 May 2018

X-linked dyskeratosis congenita

main subject

dyskeratosis congenita

1 reference

based on heuristic

inferred from title

1 reference

Jun He

1

1 reference

3 May 2018

Sandra Navarrete

2

1 reference

3 May 2018

Murek Jasinski

3

1 reference

3 May 2018

Tom Vulliamy

4

1 reference

3 May 2018

Inderjeet Dokal

5

1 reference

3 May 2018

Monica Bessler

6

1 reference

3 May 2018

Philip J Mason

7

1 reference

3 May 2018

language of work or name

English

0 references

publication date

1 October 2002

1 reference

3 May 2018

published in

Oncogene

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3 May 2018

volume

21

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3 May 2018

page(s)

7740-7744

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3 May 2018

issue

50

1 reference

3 May 2018

https://scigraph.springernature.com/pub.10.1038/sj.onc.1205969

exact match

0 references

cites work

Telomere shortening and tumor formation by mouse cells lacking telomerase RNA

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The yeast nucleolar protein Cbf5p is involved in rRNA biosynthesis and interacts genetically with the RNA polymerase I transcription factor RRN3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205969

minifly, a Drosophila gene required for ribosome biogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205969

X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functions

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205969

Wild-derived inbred mouse strains have short telomeres

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205969

X inactivation and somatic cell selection rescue female mice carrying a Piga-null mutation

21 January 2018

1 reference

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Unexplained aplastic anaemia, immunodeficiency, and cerebellar hypoplasia (Hoyeraal-Hreidarsson syndrome) due to mutations in the dyskeratosis congenita gene, DKC1

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205969

X-linked dyskeratosis congenita is predominantly caused by missense mutations in the DKC1 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205969

Identification of novel DKC1 mutations in patients with dyskeratosis congenita: implications for pathophysiology and diagnosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205969

The box H + ACA snoRNAs carry Cbf5p, the putative rRNA pseudouridine synthase

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205969

Efficient in vivo manipulation of mouse genomic sequences at the zygote stage

21 January 2018

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The telomerase reverse transcriptase is limiting and necessary for telomerase function in vivo.

21 January 2018

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Improved reporter strain for monitoring Cre recombinase-mediated DNA excisions in mice

21 January 2018

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Dyskeratosis congenita, telomeres and human ageing

21 January 2018

1 reference

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An upstream, DNase I hypersensitive region of the hematopoietic-expressed transcription factor GATA-1 gene confers developmental specificity in transgenic mice

21 January 2018

1 reference

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A box H/ACA small nucleolar RNA-like domain at the human telomerase RNA 3' end

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205969

A telomerase component is defective in the human disease dyskeratosis congenita

21 January 2018

1 reference

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Telomerase: Dr Jekyll or Mr Hyde?

21 January 2018

1 reference

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CpG methylation, chromatin structure and gene silencing-a three-way connection

21 January 2018

1 reference

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Functional importance of motif I of pseudouridine synthases: mutagenesis of aligned lysine and proline residues

21 January 2018

1 reference

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The RNA component of telomerase is mutated in autosomal dominant dyskeratosis congenita

21 January 2018

1 reference

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Very short telomeres in the peripheral blood of patients with X-linked and autosomal dyskeratosis congenita

21 January 2018

1 reference

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Point mutations in yeast CBF5 can abolish in vivo pseudouridylation of rRNA

21 January 2018

1 reference

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Association between aplastic anaemia and mutations in telomerase RNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205969

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/SJ.ONC.1205969

1 reference

3 May 2018

PubMed ID

12400016

1 reference

3 May 2018