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3.4.2 Gene studies (140)

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71403 Identification of TP53BP2 as a Novel Candidate Gene for Primary Open Angle Glaucoma by Whole Exome Sequencing in a Large Multiplex Family
Micheal S
Molecular Neurobiology 2017; 0:
71618 The GG genotype of the HSPA1B gene is associated with increased risk of glaucoma in northern Iran
Salehi Z
Molekuliarnaia biologiia 2017; 51: 31-36
71295 Selection of suitable reference genes for quantitative real-time PCR in trabecular meshwork cells under oxidative stress
Zhao J
Free radical research 2017; 51: 103-111
71488 Cyp1b1 Regulates Ocular Fissure Closure Through a Retinoic Acid-Independent Pathway
Williams AL
Investigative Ophthalmology and Visual Science 2017; 58: 1084-1097
71546 Characterizing the "POAGome": A bioinformatics-driven approach to primary open-angle glaucoma
Danford ID
Progress in Retinal and Eye Research 2017; 0:
71577 Characterization of the Circumlimbal Suture Model of Chronic IOP Elevation in Mice and Assessment of Changes in Gene Expression of Stretch Sensitive Channels
Zhao D
Frontiers in neuroscience 2017; 11: 41
71522 Association of Toll-like receptor 4 single-nucleotide polymorphisms Asp299Gly and Thr399Ile with the risk of primary open angle glaucoma
Navarro-Partida J
Graefe's Archive for Clinical and Experimental Ophthalmology 2017; 0:
71085 Association of Lysyl Oxidase-Like 1 Gene Polymorphism in Turkish Patients With Pseudoexfoliation Syndrome and Pseudoexfoliation Glaucoma
Asfuroglu M
Journal of Glaucoma 2017; 26: e54-e57
71358 Oxidative DNA damage and reduced expression of DNA repair genes: Role in primary open angle glaucoma (POAG)
Mohanty K
Ophthalmic Genetics 2017; 0: 1-5
71365 BetaB2-crystallin mutations associated with cataract and glaucoma leads to mitochondrial alterations in lens epithelial cells and retinal neurons
Dulle JE
Experimental Eye Research 2017; 155: 85-90
71575 Genetic dissection of anterior segment dysgenesis caused by a Col4a1 mutation
Mao M
Disease models & mechanisms 2017; 0:
71655 Whole exome sequencing implicates eye development, the unfolded protein response and plasma membrane homeostasis in primary open-angle glaucoma
Zhou T
PLoS ONE 2017; 12: e0172427
71620 Extended clinical features associated with novel Glis3 mutation: a case report
Alghamdi KA
BMC endocrine disorders 2017; 17: 14
71510 Epigenetics and Signaling Pathways in Glaucoma
Gauthier AC
BioMed research international 2017; 2017: 5712341
71412 Lack of association between polymorphism rs540782 and primary open angle glaucoma in Saudi patients
Kondkar AA
Journal of negative results in biomedicine 2017; 16: 3
71413 Myocilin expression is regulated by retinoic acid in the trabecular meshwork-derived cellular environment
Prat C
Experimental Eye Research 2017; 155: 91-98
71253 New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics
Springelkamp H
Human Molecular Genetics 2017; 0:
71241 BAX to basics: How the BCL2 gene family controls the death of retinal ganglion cells
Maes ME
Progress in Retinal and Eye Research 2017; 0:
71546 Characterizing the "POAGome": A bioinformatics-driven approach to primary open-angle glaucoma
Verkuil LD
Progress in Retinal and Eye Research 2017; 0:
71241 BAX to basics: How the BCL2 gene family controls the death of retinal ganglion cells
Schlamp CL
Progress in Retinal and Eye Research 2017; 0:
71085 Association of Lysyl Oxidase-Like 1 Gene Polymorphism in Turkish Patients With Pseudoexfoliation Syndrome and Pseudoexfoliation Glaucoma
Cavdarli B
Journal of Glaucoma 2017; 26: e54-e57
71253 New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics
Iglesias AI
Human Molecular Genetics 2017; 0:
71295 Selection of suitable reference genes for quantitative real-time PCR in trabecular meshwork cells under oxidative stress
Zhou H
Free radical research 2017; 51: 103-111
71403 Identification of TP53BP2 as a Novel Candidate Gene for Primary Open Angle Glaucoma by Whole Exome Sequencing in a Large Multiplex Family
Saksens NT
Molecular Neurobiology 2017; 0:
71365 BetaB2-crystallin mutations associated with cataract and glaucoma leads to mitochondrial alterations in lens epithelial cells and retinal neurons
Rübsam A
Experimental Eye Research 2017; 155: 85-90

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