A de novo Alu insertion results in neurofibromatosis type 1 (Q28281046)

From Wikidata

Jump to navigation Jump to search

scientific article

Language	Label	Description	Also known as
English	A de novo Alu insertion results in neurofibromatosis type 1	scientific article

Statements

scholarly article

0 references

A de novo Alu insertion results in neurofibromatosis type 1 (English)

0 references

0 references

author name string

M R Wallace

1

0 references

L B Andersen

2

0 references

A M Saulino

3

0 references

P E Gregory

4

0 references

T W Glover

5

0 references

F S Collins

6

0 references

language of work or name

0 references

publication date

31 October 1991

0 references

0 references

353

0 references

6347

0 references

864-6

0 references

describes a project that uses

0 references

Type 1 neurofibromatosis gene: identification of a large transcript disrupted in three NF1 patients

1 reference

https://api.crossref.org/works/10.1038%2F353864A0

7 January 2021

based on heuristic

inferred from DOI database lookup

A major segment of the neurofibromatosis type 1 gene: cDNA sequence, genomic structure, and point mutations

1 reference

https://api.crossref.org/works/10.1038%2F353864A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Deletions and a translocation interrupt a cloned gene at the neurofibromatosis type 1 locus.

1 reference

https://api.crossref.org/works/10.1038%2F353864A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Integration site preferences of the Alu family and similar repetitive DNA sequences.

1 reference

https://api.crossref.org/works/10.1038%2F353864A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Paternal origin of new mutations in von Recklinghausen neurofibromatosis.

1 reference

https://api.crossref.org/works/10.1038%2F353864A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Duplication of seven exons in LDL receptor gene caused by Alu-Alu recombination in a subject with familial hypercholesterolemia

1 reference

https://api.crossref.org/works/10.1038%2F353864A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Adenosine deaminase (ADA) deficiency due to deletion of the ADA gene promoter and first exon by homologous recombination between two Alu elements

1 reference

https://api.crossref.org/works/10.1038%2F353864A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Identical 3250-bp deletion between two AluI repeats in the ADA genes of unrelated ADA-SCID patients

1 reference

https://api.crossref.org/works/10.1038%2F353864A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Splice-mediated insertion of an Alu sequence inactivates ornithine delta-aminotransferase: a role for Alu elements in human mutation

1 reference

https://api.crossref.org/works/10.1038%2F353864A0

7 January 2021

based on heuristic

inferred from DOI database lookup

A transpositionally and transcriptionally competent Alu subfamily

1 reference

https://api.crossref.org/works/10.1038%2F353864A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Recently transposed Alu repeats result from multiple source genes.

1 reference

https://api.crossref.org/works/10.1038%2F353864A0

7 January 2021

based on heuristic

inferred from DOI database lookup

A human-specific subfamily of Alu sequences.

1 reference

https://api.crossref.org/works/10.1038%2F353864A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Amplification dynamics of human-specific (HS) alu family members

1 reference

https://api.crossref.org/works/10.1038%2F353864A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Sequence conservation in Alu evolution.

1 reference

https://api.crossref.org/works/10.1038%2F353864A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Reconstruction and analysis of human alu genes

1 reference

https://api.crossref.org/works/10.1038%2F353864A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Molecular basis of human von Willebrand disease: analysis of platelet von Willebrand factor mRNA.

1 reference

https://api.crossref.org/works/10.1038%2F353864A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

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=Q28281046&oldid=2175204645"