Identification of a gene that causes primary open angle glaucoma.
about
Evaluation of the OPTC gene in primary open angle glaucoma: functional significance of a silent changeMutations of the forkhead/winged-helix gene, FKHL7, in patients with Axenfeld-Rieger anomaly.The current research status of normal tension glaucomaProtein profile of exosomes from trabecular meshwork cellsVariants in ASB10 are associated with open-angle glaucomaRho GTPase and cAMP/protein kinase A signaling mediates myocilin-induced alterations in cultured human trabecular meshwork cellsMyocilin, a glaucoma-associated protein, promotes cell migration through activation of integrin-focal adhesion kinase-serine/threonine kinase signaling pathwayOverexpression of optineurin E50K disrupts Rab8 interaction and leads to a progressive retinal degeneration in miceMyocilin mediates myelination in the peripheral nervous system through ErbB2/3 signalingMyocilin is a modulator of Wnt signalingDifferential effects of myocilin and optineurin, two glaucoma genes, on neurite outgrowthEvidence for RPGRIP1 gene as risk factor for primary open angle glaucomaOlfactomedin 2: expression in the eye and interaction with other olfactomedin domain-containing proteinsMyocilin stimulates osteogenic differentiation of mesenchymal stem cells through mitogen-activated protein kinase signalingMutations in MTMR13, a new pseudophosphatase homologue of MTMR2 and Sbf1, in two families with an autosomal recessive demyelinating form of Charcot-Marie-Tooth disease associated with early-onset glaucomaA spectrum of FOXC1 mutations suggests gene dosage as a mechanism for developmental defects of the anterior chamber of the eyeLack of association of mutations in optineurin with disease in patients with adult-onset primary open-angle glaucomaMutations in CYP1B1, the gene for cytochrome P4501B1, are the predominant cause of primary congenital glaucoma in Saudi ArabiaLocalization of the fourth locus (GLC1E) for adult-onset primary open-angle glaucoma to the 10p15-p14 region.Identification of a novel mutation in the NTF4 gene that causes primary open-angle glaucoma in a Chinese populationDigenic inheritance of early-onset glaucoma: CYP1B1, a potential modifier geneFine mapping of new glaucoma locus GLC1M and exclusion of neuregulin 2 as the causative geneHeterozygous NTF4 mutations impairing neurotrophin-4 signaling in patients with primary open-angle glaucomaExpression of cell surface transmembrane carbonic anhydrase genes CA9 and CA12 in the human eye: overexpression of CA12 (CAXII) in glaucomaCharacterization of rabbit myocilin: Implications for human myocilin glycosylation and signal peptide usageConcise Review: Patient-Specific Stem Cells to Interrogate Inherited Eye DiseaseA molecular mechanism for glaucoma: endoplasmic reticulum stress and the unfolded protein responseOlfactomedin proteins: central players in development and diseaseRegulation of intraocular pressure by soluble and membrane guanylate cyclases and their role in glaucomaCurrent understanding of conventional outflow dysfunction in glaucomaCurrent concepts on primary open-angle glaucoma genetics: a contribution to disease pathophysiology and future treatmentGenetic, Biochemical and Clinical Insights into Primary Congenital GlaucomaA Mutation in LTBP2 Causes Congenital Glaucoma in Domestic Cats (Felis catus)The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25hOLF44, a secreted glycoprotein with distinct expression pattern, belongs to an uncharacterized olfactomedin-like subfamily newly identified by phylogenetic analysisCommon variants near ABCA1, AFAP1 and GMDS confer risk of primary open-angle glaucomaCystatin a, a potential common link for mutant myocilin causative glaucomaCyp1b1 mediates periostin regulation of trabecular meshwork development by suppression of oxidative stressOlfactomedin 4 down-regulates innate immunity against Helicobacter pylori infectionDeletion of olfactomedin 2 induces changes in the AMPA receptor complex and impairs visual, olfactory, and motor functions in mice
P2860
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P2860
Identification of a gene that causes primary open angle glaucoma.
description
1997 nî lūn-bûn
@nan
1997 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1997 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
name
Identification of a gene that causes primary open angle glaucoma.
@ast
Identification of a gene that causes primary open angle glaucoma.
@en
Identification of a gene that causes primary open angle glaucoma.
@nl
type
label
Identification of a gene that causes primary open angle glaucoma.
@ast
Identification of a gene that causes primary open angle glaucoma.
@en
Identification of a gene that causes primary open angle glaucoma.
@nl
prefLabel
Identification of a gene that causes primary open angle glaucoma.
@ast
Identification of a gene that causes primary open angle glaucoma.
@en
Identification of a gene that causes primary open angle glaucoma.
@nl
P2093
P50
P1433
P1476
Identification of a gene that causes primary open angle glaucoma
@en
P2093
B E Nichols
D A Mackey
D Nishimura
J R Polansky
J W Kalenak
S L Sunden
T D Nguyen
P304
P356
10.1126/SCIENCE.275.5300.668
P407
P577
1997-01-01T00:00:00Z