(Q45877644)

17 December 2017

title

Frequency of recent retrotransposition events in the human factor IX gene (English)

1 reference

17 December 2017

author name string

Li X

1

1 reference

17 December 2017

Scaringe WA

2

1 reference

17 December 2017

Hill KA

3

1 reference

17 December 2017

Roberts S

4

1 reference

17 December 2017

Mengos A

5

1 reference

17 December 2017

Careri D

6

1 reference

17 December 2017

Pinto MT

7

1 reference

17 December 2017

Kasper CK

8

1 reference

17 December 2017

Sommer SS

9

1 reference

17 December 2017

publication date

1 June 2001

1 reference

17 December 2017

published in

Human Mutation

1 reference

17 December 2017

volume

17

1 reference

17 December 2017

page(s)

511-519

1 reference

17 December 2017

issue

6

1 reference

17 December 2017

Gapped BLAST and PSI-BLAST: a new generation of protein database search programs

cites work

1 reference

Standardized nomenclature for Alu repeats.

21 January 2018

1 reference

The pattern of spontaneous germ-line mutation: relative rates of mutation at or near CpG dinucleotides in the factor IX gene

21 January 2018

1 reference

Alu repeats and human disease

21 January 2018

1 reference

High genomic deleterious mutation rates in hominids

21 January 2018

1 reference

The Pennsylvania hemophilia program 1973-1978.

21 January 2018

1 reference

The rate of spontaneous mutation of a human gene

21 January 2018

1 reference

Hereditary desmoid disease in a family with a germline Alu I repeat mutation of the APC gene

21 January 2018

1 reference

A new subfamily of recently retroposed human Alu repeats

21 January 2018

1 reference

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

21 January 2018

1 reference

Insertion of a 5' truncated L1 element into the 3' end of exon 44 of the dystrophin gene resulted in skipping of the exon during splicing in a case of Duchenne muscular dystrophy

21 January 2018

1 reference

The rate with which spontaneous mutation alters the electrophoretic mobility of polypeptides

21 January 2018

1 reference

De novo alu-element insertions in FGFR2 identify a distinct pathological basis for Apert syndrome

21 January 2018

1 reference

Potential Gene Conversion and Source Genes for Recently Integrated Alu Elements

21 January 2018

1 reference

Unit-length line-1 transcripts in human teratocarcinoma cells

21 January 2018

1 reference

The factor IX gene as a model for analysis of human germline mutations: an update

21 January 2018

1 reference

Genomic amplification with transcript sequencing

21 January 2018

1 reference

A de novo Alu insertion results in neurofibromatosis type 1

21 January 2018

1 reference

Detection of polymorphisms at cytosine phosphoguanadine dinucleotides and diagnosis of haemophilia B carriers

21 January 2018

1 reference

Identification of a novel large F9 gene mutation-an insertion of an Alu repeated DNA element in exon e of the factor 9 gene

21 January 2018

1 reference

The recent evolution of mammalian repetitive DNA elements

21 January 2018

1 reference

L1 (LINE-1) retrotransposon evolution and amplification in recent human history

21 January 2018

1 reference

7 January 2021

Parameters affecting the yield of DNA from human blood

1 reference

7 January 2021

An estimated frequency of endogenous insertional mutations in humans

1 reference

7 January 2021

1 reference

7 January 2021

Dideoxy fingerprinting (ddF): A rapid and efficient screen for the presence of mutations

1 reference

7 January 2021

Haemophilia B due to a de novo insertion of a human-specific Alu subfamily member within the coding region of the factor IX gene

1 reference

7 January 2021

Identifiers

DOI

10.1002/HUMU.1134

1 reference

17 December 2017

PubMed ID

11385709

1 reference

17 December 2017