review article | Q7318358 |
scholarly article | Q13442814 |
P2093 | author name string | M Roy Wilson | |
Gordon Gong | |||
Omofolasade Kosoko-Lasaki | |||
Gleb R Haynatzki | |||
P304 | page(s) | R91-102 | |
P577 | publication date | 2004-02-05 | |
P1433 | published in | Human Molecular Genetics | Q2720965 |
P1476 | title | Genetic dissection of myocilin glaucoma. | |
P478 | volume | 13 Spec No 1 |
Q36499353 | Absence of optineurin (OPTN) gene mutations in Taiwanese patients with juvenile-onset open-angle glaucoma. |
Q35918465 | Accurate Imputation-Based Screening of Gln368Ter Myocilin Variant in Primary Open-Angle Glaucoma |
Q35881767 | Amyloid fibril formation by the glaucoma-associated olfactomedin domain of myocilin |
Q33808845 | Biophysical characterization of the olfactomedin domain of myocilin, an extracellular matrix protein implicated in inherited forms of glaucoma |
Q40103210 | Characterization of the intracellular proteolytic cleavage of myocilin and identification of calpain II as a myocilin-processing protease. |
Q46899245 | Circadian changes of intraocular pressure and ocular perfusion pressure after timolol or latanoprost in Caucasians with normal-tension glaucoma |
Q35940374 | Clinical features associated with an Asp380His Myocilin mutation in a US family with primary open-angle glaucoma |
Q42636014 | Cloning of canine myocilin cDNA and molecular analysis of the myocilin gene in Shiba Inu dogs |
Q37819720 | Complex genetic mechanisms in glaucoma: an overview |
Q36499378 | Contributions of MYOC and CYP1B1 mutations to JOAG |
Q27015027 | Current concepts on primary open-angle glaucoma genetics: a contribution to disease pathophysiology and future treatment |
Q28483730 | Cystatin a, a potential common link for mutant myocilin causative glaucoma |
Q91887225 | Differential Misfolding Properties of Glaucoma-Associated Olfactomedin Domains from Humans and Mice |
Q24329037 | Differential effects of myocilin and optineurin, two glaucoma genes, on neurite outgrowth |
Q37126077 | Dual localization of wild-type myocilin in the endoplasmic reticulum and extracellular compartment likely occurs due to its incomplete secretion. |
Q33705286 | Evaluation of MYOC, ACAN, HGF, and MET as candidate genes for high myopia in a Han Chinese population |
Q24336657 | Evidence for RPGRIP1 gene as risk factor for primary open angle glaucoma |
Q33882506 | Expression of myocilin mutants sensitizes cells to oxidative stress-induced apoptosis: implication for glaucoma pathogenesis |
Q38966980 | Genetic and Biochemical Biomarkers in Canine Glaucoma. |
Q35208924 | Genetic association of SNPs near ATOH7, CARD10, CDKN2B, CDC7 and SIX1/SIX6 with the endophenotypes of primary open angle glaucoma in Indian population |
Q39010214 | Genetic variants associated with primary open angle glaucoma in Indian population |
Q27022047 | Genetic, Biochemical and Clinical Insights into Primary Congenital Glaucoma |
Q36075362 | Glaucomatous MYOC mutations activate the IL-1/NF-κB inflammatory stress response and the glaucoma marker SELE in trabecular meshwork cells |
Q36418920 | Glucose-regulated protein 94 triage of mutant myocilin through endoplasmic reticulum-associated degradation subverts a more efficient autophagic clearance mechanism |
Q24657994 | Heterozygous NTF4 mutations impairing neurotrophin-4 signaling in patients with primary open-angle glaucoma |
Q36978194 | Heterozygous expression of myocilin glaucoma mutants increases secretion of the mutant forms and reduces extracellular processed myocilin. |
Q34081392 | Identification a novel MYOC gene mutation in a Chinese family with juvenile-onset open angle glaucoma |
Q28590582 | Identification and characterization of photomedins: novel olfactomedin-domain-containing proteins with chondroitin sulphate-E-binding activity |
Q28573610 | Interaction between two glaucoma genes, optineurin and myocilin |
Q42250281 | Key molecular pathways affected by glaucoma pathology: is predictive diagnosis possible? |
Q37119238 | Linkage and association of myocilin (MYOC) polymorphisms with high myopia in a Chinese population |
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Q34208364 | MYOC and FOXC1 gene analysis in primary congenital glaucoma |
Q46150477 | MYOC mutations in black south african patients with primary open-angle glaucoma: genetic testing and cascade screening. |
Q24306535 | Mitochondrial association of myocilin, product of a glaucoma gene, in human trabecular meshwork cells |
Q28545946 | Molecular Details of Olfactomedin Domains Provide Pathway to Structure-Function Studies |
Q36543270 | Molecular Diagnostics and Genetic Counseling in Primary Congenital Glaucoma |
Q36216651 | Molecular biology and surgical practice. |
Q37054960 | Multiple gene polymorphisms analysis revealed a different profile of genetic polymorphisms of primary open-angle glaucoma in northern Chinese |
Q30420204 | Mutations in the CYP1B1 gene may contribute to juvenile-onset open-angle glaucoma |
Q42379452 | Myocilin Regulates Metalloprotease 2 Activity Through Interaction With TIMP3. |
Q37249806 | Myocilin and Optineurin: Differential Characteristics and Functional Consequences |
Q24328948 | Myocilin is a modulator of Wnt signaling |
Q35629081 | Myocilin mutations among POAG patients from two populations of Tamil Nadu, South India, a comparative analysis |
Q34912544 | Myocilin mutations in black South Africans with POAG. |
Q34431440 | Myocilin polymorphisms and primary open-angle glaucoma: a systematic review and meta-analysis. |
Q37683314 | Myocilin regulates cell proliferation and survival |
Q51536319 | New direction for glaucoma therapeutics: focus on the olfactomedin domain of myocilin. |
Q42630980 | New mutation in the MYOC gene and its association with primary open-angle glaucoma in a Chinese family |
Q36145931 | Novel and known MYOC exon 3 mutations in an admixed Peruvian primary open-angle glaucoma population |
Q35697197 | Optimedin induces expression of N-cadherin and stimulates aggregation of NGF-stimulated PC12 cells |
Q36143392 | Optimized bacterial expression of myocilin proteins and functional comparison of bacterial and eukaryotic myocilins. |
Q30244246 | Presence and Risk Factors for Glaucoma in Patients with Diabetes |
Q37874443 | Primary open-angle glaucoma genes. |
Q37159445 | Pro370Leu mutant myocilin disturbs the endoplasm reticulum stress response and mitochondrial membrane potential in human trabecular meshwork cells. |
Q37166653 | Pro370Leu mutant myocilin impairs mitochondrial functions in human trabecular meshwork cells. |
Q35032291 | Pro370Leu myocilin mutation in a Chinese pedigree with juvenile-onset open angle glaucoma. |
Q40569319 | Reversal of mutant myocilin non-secretion and cell killing: implications for glaucoma |
Q24299747 | Rho GTPase and cAMP/protein kinase A signaling mediates myocilin-induced alterations in cultured human trabecular meshwork cells |
Q35234500 | Ser341Pro MYOC gene mutation in a family with primary open-angle glaucoma |
Q42225116 | Significance of G-X-W motif in the myocilin olfactomedin domain |
Q38963936 | Steroid-induced ocular hypertension/glaucoma: Focus on pharmacogenomics and implications for precision medicine |
Q35234066 | Structural basis for misfolding in myocilin-associated glaucoma |
Q37071359 | Survey of familial glaucoma shows a high incidence of cytochrome P450, family 1, subfamily B, polypeptide 1 (CYP1B1) mutations in non-consanguineous congenital forms in a Spanish population |
Q38572659 | Targeting the ER-autophagy system in the trabecular meshwork to treat glaucoma |
Q28575796 | The Optimedin gene is a downstream target of Pax6 |
Q37710660 | The effects of myocilin expression on functionally relevant trabecular meshwork genes: a mini-review |
Q30356731 | The glaucoma-associated olfactomedin domain of myocilin forms polymorphic fibrils that are constrained by partial unfolding and peptide sequence |
Q89928596 | The impact of anthropometric and ocular parameters on optic cup-to-disc ratio |
Q92000114 | The mutational spectrum of Myocilin gene among familial versus sporadic cases of Juvenile onset open angle glaucoma |
Q37362502 | The novel Y371D myocilin mutation causes an aggressive form of juvenile open-angle glaucoma in a Caucasian family from the Middle-East |
Q35083487 | The stability of myocilin olfactomedin domain variants provides new insight into glaucoma as a protein misfolding disorder |
Q33602666 | Transgenic mice expressing the Tyr437His mutant of human myocilin protein develop glaucoma |
Q36864324 | Two novel myocilin mutations in a Chinese family with primary open-angle glaucoma. |
Q35919067 | Unaltered myocilin expression in the blood of primary open angle glaucoma patients |
Q54449559 | Variable clinical spectrum of the myocilin Gln368X mutation in a Dutch family with primary open angle glaucoma. |
Q34427630 | Wnt activation by wild type and mutant myocilin in cultured human trabecular meshwork cells |
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