Human ameloblastin gene: genomic organization and mutation analysis in amelogenesis imperfecta patients (Q60458166)

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7 November 2019

title

Human ameloblastin gene: genomic organization and mutation analysis in amelogenesis imperfecta patients (English)

1 reference

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7 November 2019

main subject

amelogenesis imperfecta

1 reference

4

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7 November 2019

author name string

C K Mårdh

1

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7 November 2019

B Bäckman

2

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7 November 2019

D Simmons

3

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7 November 2019

T T Gu

5

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7 November 2019

G Holmgren

6

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7 November 2019

M MacDougall

7

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7 November 2019

K Forsman-Semb

8

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7 November 2019

publication date

1 February 2001

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European Journal of Oral Sciences

7 November 2019

published in

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7 November 2019

volume

109

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7 November 2019

issue

1

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7 November 2019

page(s)

8-13

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Amelogenin signal peptide mutation: correlation between mutations in the amelogenin gene (AMGX) and manifestations of X-linked amelogenesis imperfecta

7 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0722.2001.00979.X

An amelogenin gene defect associated with human X-linked amelogenesis imperfecta

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0722.2001.00979.X

Full-length sequence, localization, and chromosomal mapping of ameloblastin. A novel tooth-specific gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0722.2001.00979.X

Cloning, characterization and immunolocalization of human ameloblastin

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0722.2001.00979.X

Sheath proteins: synthesis, secretion, degradation and fate in forming enamel

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0722.2001.00979.X

Mapping of the locus for autosomal dominant amelogenesis imperfecta (AIH2) to a 4-Mb YAC contig on chromosome 4q11-q21

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0722.2001.00979.X

Ameloblastin gene (AMBN) maps within the critical region for autosomal dominant amelogenesis imperfecta at chromosome 4q21.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0722.2001.00979.X

Genetic heterogeneity of autosomal dominant amelogenesis imperfecta demonstrated by its exclusion from the AIH2 region on human chromosome 4Q

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0722.2001.00979.X

DNA sequences of amelogenin genes provide clues to regulation of expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0722.2001.00979.X

PCR-SSCP: a method for detection of mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0722.2001.00979.X

A deletion in the amelogenin gene (AMG) causes X-linked amelogenesis imperfecta (AIH1)

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0722.2001.00979.X

7 January 2021

SSCP detection of a nonsense mutation in exon 5 of the amelogenin gene (AMGX) causing X-linked amelogenesis imperfecta (AIH1)

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0722.2001.00979.X

7 January 2021

A novel gene expressed in rat ameloblasts codes for proteins with cell binding domains

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0722.2001.00979.X

7 January 2021

Identification and characterization of a cDNA for mouse ameloblastin

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0722.2001.00979.X

7 January 2021

Sheathlin: cloning, cDNA/polypeptide sequences, and immunolocalization of porcine enamel sheath proteins

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0722.2001.00979.X

7 January 2021

Localization of a gene for autosomal dominant amelogenesis imperfecta (ADAI) to chromosome 4q.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0722.2001.00979.X

7 January 2021

Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0722.2001.00979.X

7 January 2021

Amelogenesis imperfecta: a genetic study

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0722.2001.00979.X

7 January 2021

Enamelin maps to human chromosome 4q21 within the autosomal dominant amelogenesis imperfecta locus

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0722.2001.00979.X

7 January 2021

Cloning human enamelin cDNA, chromosomal localization, and analysis of expression during tooth development

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0722.2001.00979.X

7 January 2021

10.1034/J.1600-0722.2001.00979.X

Identifiers

DOI

1 reference

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7 November 2019

1 reference