Haemophilia A resulting from de novo insertion of L1 sequences represents a novel mechanism for mutation in man. (Q34553577)

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English	Haemophilia A resulting from de novo insertion of L1 sequences represents a novel mechanism for mutation in man.	scientific article

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scholarly article

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Europe PubMed Central

PubMed publication ID

3 August 2017

Haemophilia A resulting from de novo insertion of L1 sequences represents a novel mechanism for mutation in man. (English)

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Europe PubMed Central

PubMed publication ID

3 August 2017

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Stilianos Antonarakis

6

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Antonarakis SE

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3 August 2017

author name string

Kazazian HH Jr

1

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Europe PubMed Central

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3 August 2017

Wong C

2

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Europe PubMed Central

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3 August 2017

Youssoufian H

3

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Europe PubMed Central

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3 August 2017

Scott AF

4

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3 August 2017

Phillips DG

5

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3 August 2017

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publication date

1 March 1988

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3 August 2017

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3 August 2017

332

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3 August 2017

6160

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3 August 2017

164-166

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Europe PubMed Central

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3 August 2017

Origin of the human L1 elements: proposed progenitor genes deduced from a consensus DNA sequence

1 reference

https://api.crossref.org/works/10.1038%2F332164A0

7 January 2021

based on heuristic

inferred from DOI database lookup

L1 family of repetitive DNA sequences in primates may be derived from a sequence encoding a reverse transcriptase-related protein

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https://api.crossref.org/works/10.1038%2F332164A0

7 January 2021

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Expression of a cytoplasmic LINE-1 transcript is regulated in a human teratocarcinoma cell line

1 reference

https://api.crossref.org/works/10.1038%2F332164A0

7 January 2021

based on heuristic

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The abundant LINE-1 family of repeated DNA sequences in mammals: genes and pseudogenes

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https://api.crossref.org/works/10.1038%2F332164A0

7 January 2021

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Characterization of the human factor VIII gene

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https://api.crossref.org/works/10.1038%2F332164A0

7 January 2021

based on heuristic

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Molecular cloning of a cDNA encoding human antihaemophilic factor

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https://api.crossref.org/works/10.1038%2F332164A0

7 January 2021

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Detection and sequence of mutations in the factor VIII gene of haemophiliacs

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https://api.crossref.org/works/10.1038%2F332164A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Recurrent mutations in haemophilia A give evidence for CpG mutation hotspots

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7 January 2021

based on heuristic

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DNA sequencing with chain-terminating inhibitors

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7 January 2021

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A Chinese G gamma + (A gamma delta beta)zero thalassemia deletion: comparison to other deletions in the human beta-globin gene cluster and sequence analysis of the breakpoints

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7 January 2021

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Related polypeptides are encoded by Drosophila F elements, I factors, and mammalian L1 sequences

1 reference

https://api.crossref.org/works/10.1038%2F332164A0

7 January 2021

based on heuristic

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A family of oligo-adenylate-terminated transposable sequences in Drosophila melanogaster

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

"Retroposon" insertion into the cellular oncogene c-myc in canine transmissible venereal tumor

1 reference

https://api.crossref.org/works/10.1038%2F332164A0

7 January 2021

based on heuristic

inferred from DOI database lookup

The sequence of a large L1Md element reveals a tandemly repeated 5' end and several features found in retrotransposons

1 reference

https://api.crossref.org/works/10.1038%2F332164A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Rat LINE1: the origin and evolution of a family of long interspersed middle repetitive DNA elements

1 reference

https://api.crossref.org/works/10.1038%2F332164A0

7 January 2021

based on heuristic

inferred from DOI database lookup

A family of long reiterated DNA sequences, one copy of which is next to the human beta globin gene

1 reference

https://api.crossref.org/works/10.1038%2F332164A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/332164A0

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

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PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

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