Identification of the gene responsible for gelatinous drop-like corneal dystrophy
about
Tumor-associated calcium signal transducer 2 is required for the proper subcellular localization of claudin 1 and 7: implications in the pathogenesis of gelatinous drop-like corneal dystrophyIdentification of CRYM as a candidate responsible for nonsyndromic deafness, through cDNA microarray analysis of human cochlear and vestibular tissues.The IC3D classification of the corneal dystrophiesCharacteristics of corneal dystrophies: a review from clinical, histological and genetic perspectivesIdentification and characterization of a novel TACSTD2 mutation in gelatinous drop-like corneal dystrophy.A novel TACSTD2 mutation identified in two Chinese brothers with gelatinous drop-like corneal dystrophy.Protein-Coding Genes' Retrocopies and Their Functions.Mobile elements in the human genome: implications for diseaseEvolutionary fate of retroposed gene copies in the human genomeTwo novel mutations of TACSTD2 found in three Japanese gelatinous drop-like corneal dystrophy families with their aberrant subcellular localization.Regulated intramembrane proteolysis and degradation of murine epithelial cell adhesion molecule mEpCAM.Current gene discovery strategies for ocular conditionsApolipoproteins J and E co-localise with amyloid in gelatinous drop-like and lattice type I corneal dystrophies.Lactoferrin Glu561Asp facilitates secondary amyloidosis in the cornea.Loss of Trop2 promotes carcinogenesis and features of epithelial to mesenchymal transition in squamous cell carcinoma.Localization of a gene for nonsyndromic renal hypodysplasia to chromosome 1p32-33Co-localisation of advanced glycation end products and D-β-aspartic acid-containing proteins in gelatinous drop-like corneal dystrophy.Inherited corneal disease: the evolving molecular, genetic and imaging revolution.TROP2 is epigenetically inactivated and modulates IGF-1R signalling in lung adenocarcinoma.Atypical asymmetric lattice corneal dystrophy associated with a novel homozygous mutation (Val624Met) in the TGFBI gene.A novel mutation (p.Glu1389AspfsX16) of the phosphoinositide kinase, FYVE finger containing gene found in a Japanese patient with fleck corneal dystrophy"Orphan" retrogenes in the human genome.Novel TACSTD2 mutation in gelatinous drop-like corneal dystrophy.Trop2 is overexpressed in gastric cancer and predicts poor prognosis.Trop2 identifies a subpopulation of murine and human prostate basal cells with stem cell characteristics.DNA variations in human and medical genetics: 25 years of my experience.Two novel mutations identified in two Chinese gelatinous drop-like corneal dystrophy families.Trop2: from development to disease.Expression of Trop2 cell surface glycoprotein in normal and tumor tissues: potential implications as a cancer therapeutic target.Trop2 inhibition suppresses the proliferation and invasion of laryngeal carcinoma cells via the extracellular signal-regulated kinase/mitogen-activated protein kinase pathway.Gelatinous drop-like corneal dystrophy: a review.Establishment of a human conjunctival epithelial cell line lacking the functional TACSTD2 gene (an American Ophthalmological Society thesis).Gelatinous drop-like corneal dystrophy with a novel mutation of TACSTD2 manifested in combination with spheroidal degeneration in a Chinese patientMouse genetic corneal disease resulting from transgenic insertional mutagenesis.Identification of calcium-inducible genes in primary keratinocytes using suppression-subtractive hybridization.Gelatinous drop-like corneal dystrophy in a child with developmental delay: clinicopathological features and exclusion of the M1S1 gene.Amphioxus SYCP1: a case of retrogene replacement and co-option of regulatory elements adjacent to the ParaHox cluster.The oncogene Trop2 regulates fetal lung cell proliferation.Infection with hepatitis C virus depends on TACSTD2, a regulator of claudin-1 and occludin highly downregulated in hepatocellular carcinoma.Novel Mutations in TACSTD2 Gene in Families with Gelatinous Drop-like Corneal Dystrophy (GDLD).
P2860
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P2860
Identification of the gene responsible for gelatinous drop-like corneal dystrophy
description
1999 nî lūn-bûn
@nan
1999 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
Identification of the gene responsible for gelatinous drop-like corneal dystrophy
@ast
Identification of the gene responsible for gelatinous drop-like corneal dystrophy
@en
Identification of the gene responsible for gelatinous drop-like corneal dystrophy
@en-gb
Identification of the gene responsible for gelatinous drop-like corneal dystrophy
@nl
type
label
Identification of the gene responsible for gelatinous drop-like corneal dystrophy
@ast
Identification of the gene responsible for gelatinous drop-like corneal dystrophy
@en
Identification of the gene responsible for gelatinous drop-like corneal dystrophy
@en-gb
Identification of the gene responsible for gelatinous drop-like corneal dystrophy
@nl
prefLabel
Identification of the gene responsible for gelatinous drop-like corneal dystrophy
@ast
Identification of the gene responsible for gelatinous drop-like corneal dystrophy
@en
Identification of the gene responsible for gelatinous drop-like corneal dystrophy
@en-gb
Identification of the gene responsible for gelatinous drop-like corneal dystrophy
@nl
P2093
P356
P1433
P1476
Identification of the gene responsible for gelatinous drop-like corneal dystrophy
@en
P2093
H Kurahashi
M Tsujikawa
Y Nakamura
Y Shimomura
P2888
P356
10.1038/7759
P407
P577
1999-04-01T00:00:00Z
P6179
1019507680