Telomerase RNA deficiency in peripheral blood mononuclear cells in X-linked dyskeratosis congenita (Q40519021)

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scientific article published on 3 September 2004

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English	Telomerase RNA deficiency in peripheral blood mononuclear cells in X-linked dyskeratosis congenita	scientific article published on 3 September 2004

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15349768

retrieved

21 September 2017

title

Telomerase RNA deficiency in peripheral blood mononuclear cells in X-linked dyskeratosis congenita (English)

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Europe PubMed Central

PubMed publication ID

15349768

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21 September 2017

author name string

Judy M Y Wong

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1

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Europe PubMed Central

PubMed publication ID

15349768

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21 September 2017

Mouhammed J Kyasa

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2

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Europe PubMed Central

PubMed publication ID

15349768

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21 September 2017

Laura Hutchins

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3

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Europe PubMed Central

PubMed publication ID

15349768

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21 September 2017

Kathleen Collins

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4

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Europe PubMed Central

PubMed publication ID

15349768

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21 September 2017

publication date

3 September 2004

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15349768

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21 September 2017

published in

Human Genetics

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stated in

Europe PubMed Central

PubMed publication ID

15349768

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21 September 2017

volume

115

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Europe PubMed Central

PubMed publication ID

15349768

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21 September 2017

issue

5

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Europe PubMed Central

PubMed publication ID

15349768

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21 September 2017

page(s)

448-455

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Europe PubMed Central

PubMed publication ID

15349768

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21 September 2017

cites work

Evolving views of telomerase and cancer

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/15349768

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Increased mortality rate and not impaired ribosomal biogenesis is responsible for proliferative defect in dyskeratosis congenita cell lines.

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15349768

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Late presentation of dyskeratosis congenita as apparently acquired aplastic anaemia due to mutations in telomerase RNA

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15349768

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12 December 2020

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inferred from PubMed ID database lookup

Structure and biogenesis of small nucleolar RNAs acting as guides for ribosomal RNA modification.

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15349768

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biochemical aspects of telomerase function

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15349768

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12 December 2020

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inferred from PubMed ID database lookup

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

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15349768

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12 December 2020

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inferred from PubMed ID database lookup

Dyskeratosis congenita

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15349768

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biogenesis of small nucleolar ribonucleoproteins

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/15349768

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Telomerase activation in mouse mammary tumors: lack of detectable telomere shortening and evidence for regulation of telomerase RNA with cell proliferation

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/15349768

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Subnuclear shuttling of human telomerase induced by transformation and DNA damage.

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/15349768

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12 December 2020

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inferred from PubMed ID database lookup

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

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15349768

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human H/ACA small nucleolar RNPs and telomerase share evolutionarily conserved proteins NHP2 and NOP10

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/15349768

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dyskeratosis congenita and cancer in mice deficient in ribosomal RNA modification

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/15349768

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12 December 2020

based on heuristic

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Telomere maintenance and disease

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/15349768

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Building 'validated' mouse models of human cancer

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/15349768

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association between aplastic anaemia and mutations in telomerase RNA

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/15349768

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The expanding snoRNA world

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/15349768

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Telomerase in the human organism

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15349768

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Distinct biogenesis pathways for human telomerase RNA and H/ACA small nucleolar RNAs

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15349768

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15349768

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Skewed X-inactivation in carriers of X-linked dyskeratosis congenita.

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/15349768

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The end of the (DNA) line

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/15349768

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human telomerase activation requires two independent interactions between telomerase RNA and telomerase reverse transcriptase

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15349768

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Telomeres, telomerase, and hematopoietic stem cell biology

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/15349768

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

In situ hybridization analysis of the expression of human telomerase RNA in normal and pathologic conditions of the skin

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15349768

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15349768

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dyskeratosis congenita: its link to telomerase and aplastic anaemia

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15349768

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Stem cells, telomerase and dyskeratosis congenita

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15349768

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

In vitro assembly of human H/ACA small nucleolar RNPs reveals unique features of U17 and telomerase RNAs

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15349768

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A telomerase component is defective in the human disease dyskeratosis congenita

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15349768

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15349768

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/S00439-004-1178-7

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15349768

retrieved

21 September 2017

Dimensions Publication ID

1046644183

0 references

PubMed publication ID

15349768

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15349768

retrieved

21 September 2017

 

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