Heterozygous triplication of upstream regulatory sequences leads to dysregulation of matrix metalloproteinase 19 in patients with cavitary optic disc anomaly.
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Intricate Functions of Matrix Metalloproteinases in Physiological and Pathological Conditions.MMP19 expression in the human optic nerve.A large family with inherited optic disc anomalies: a correlation between a new genetic locus and complex ocular phenotypesMetalloproteinases as mediators of inflammation and the eyes: molecular genetic underpinnings governing ocular pathophysiologyBiochemical and Biological Attributes of Matrix Metalloproteinases.Assessment of a three-generation pedigree with Fuchs endothelial corneal dystrophy with anticipation for expansion of the triplet repeat in the TCF4 gene.
P2860
Heterozygous triplication of upstream regulatory sequences leads to dysregulation of matrix metalloproteinase 19 in patients with cavitary optic disc anomaly.
description
2015 nî lūn-bûn
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2015年の論文
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2015年論文
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2015年論文
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2015年論文
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2015年論文
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2015年論文
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2015年论文
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name
Heterozygous triplication of u ...... h cavitary optic disc anomaly.
@en
type
label
Heterozygous triplication of u ...... h cavitary optic disc anomaly.
@en
prefLabel
Heterozygous triplication of u ...... h cavitary optic disc anomaly.
@en
P2093
P2860
P50
P356
P1433
P1476
Heterozygous triplication of u ...... h cavitary optic disc anomaly.
@en
P2093
Benjamin R Roos
Frances Solivan-Timpe
Kacie J Meyer
Lee M Jampol
Ralph J Hazlewood
Robert A Honkanen
Stephen C Gieser
P2860
P304
P356
10.1002/HUMU.22754
P50
P577
2015-03-01T00:00:00Z