(Q24606267)

2

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H-Y Kang

3

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K-E Lee

4

0 references

K Gencay

5

0 references

B Tuna

6

0 references

J-W Kim

Journal of Dental Research

7

0 references

language of work or name

English

0 references

publication date

January 2010

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published in

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volume

89

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issue

1

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page(s)

46-50

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cites work

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FAM83H mutations in families with autosomal-dominant hypocalcified amelogenesis imperfecta

7 April 2017

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MMP-20 mutation in autosomal recessive pigmented hypomaturation amelogenesis imperfecta

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Mutation in kallikrein 4 causes autosomal recessive hypomaturation amelogenesis imperfecta

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Decreased mineral content in MMP-20 null mouse enamel is prominent during the maturation stage

7 April 2017

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Amelogenin p.M1T and p.W4S mutations underlying hypoplastic X-linked amelogenesis imperfecta

7 April 2017

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Premature stop codon in MMP20 causing amelogenesis imperfecta

27 September 2017

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27 September 2017

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Enamelysin (matrix metalloproteinase 20)-deficient mice display an amelogenesis imperfecta phenotype.

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A novel missense mutation (p.P52R) in amelogenin gene causing X-linked amelogenesis imperfecta.

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The hemopexin and O-glycosylated domains tune gelatinase B/MMP-9 bioavailability via inhibition and binding to cargo receptors.

21 January 2018

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The hemopexin-like domain (C domain) of human gelatinase A (matrix metalloproteinase-2) requires Ca2+ for fibronectin and heparin binding. Binding properties of recombinant gelatinase A C domain to extracellular matrix and basement membrane componen

21 January 2018

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PubMed

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inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identification of the TIMP-2 binding site on the gelatinase A hemopexin C-domain by site-directed mutagenesis and the yeast two-hybrid system

1 reference

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https://pubmed.ncbi.nlm.nih.gov/19966041