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1دورية أكاديمية
المؤلفون: Samer Khateb, Lina Zelinger, Tamar Ben-Yosef, Saul Merin, Ornit Crystal-Shalit, Menachem Gross, Eyal Banin, Dror Sharon
المصدر: PLoS ONE, Vol 7, Iss 12, p e51566 (2012)
وصف الملف: electronic resource
العلاقة: http://europepmc.org/articles/PMC3520954?pdf=renderTest; https://doaj.org/toc/1932-6203Test
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2دورية أكاديمية
المؤلفون: Avigail Beryozkin, Lina Zelinger, Dikla Bandah-Rozenfeld, Anat Harel, Tim A Strom, Saul Merin, Itay Chowers, Eyal Banin, Dror Sharon
المساهمون: The Pennsylvania State University CiteSeerX Archives
وصف الملف: application/pdf
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3دورية أكاديمية
المؤلفون: Nancy C. Arbour, Joel Zlotogora, Robert G. Knowlton, Saul Merin, Ada Rosenmann, Adam B. Kanis, Tatiana Rokhlina, Edwin M. Stone, Val C. Sheffield
المساهمون: The Pennsylvania State University CiteSeerX Archives
وصف الملف: application/pdf
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المؤلفون: Dror Sharon, Dikla Bandah-Rozenfeld, Chen Farhy, Saul Merin, Eyal Banin, Alexey Obolensky, Tamar Ben-Yosef, Itay Chowers, Ruth Ashery-Padan, Jacob Pe'er, Liliana Mizrahi-Meissonnier
المصدر: The American Journal of Human Genetics. 87:382-391
مصطلحات موضوعية: Candidate gene, genetic structures, Fundus Oculi, DNA Mutational Analysis, Molecular Sequence Data, Genes, Recessive, Locus (genetics), Biology, Evolution, Molecular, Mice, Exon, Gene mapping, Report, Retinitis pigmentosa, Genetics, medicine, Animals, Genetics(clinical), Family, Amino Acid Sequence, Eye Proteins, Genetics (clinical), Retina, Base Sequence, Reverse Transcriptase Polymerase Chain Reaction, Homozygote, Chromosome Mapping, Gene Expression Regulation, Developmental, Disease gene identification, medicine.disease, Null allele, eye diseases, medicine.anatomical_structure, Mutation, sense organs, Retinitis Pigmentosa
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::399c9776e2fa0284c0e8acf12f333c1dTest
https://doi.org/10.1016/j.ajhg.2010.07.022Test -
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المؤلفون: Itay Chowers, Rob W.J. Collin, Dror Sharon, Marijke N. Zonneveld, L. Ingeborgh van den Born, Frans P.M. Cremers, Tamar Ben-Yosef, Karin W. Littink, Dikla Bandah-Rozenfeld, Saul Merin, Eyal Banin, Tim M. Strom, Anneke I. den Hollander
المصدر: Investigative Ophthalmology and Visual Science, 51, 4387-94
Investigative Ophthalmology and Visual Science, 51, 9, pp. 4387-94مصطلحات موضوعية: Adult, Male, Genetics and epigenetic pathways of disease [NCMLS 6], DNA Mutational Analysis, Population, Genes, Recessive, Biology, medicine.disease_cause, Genomic disorders and inherited multi-system disorders [IGMD 3], Young Adult, Retinitis pigmentosa, Electroretinography, medicine, Humans, Israel, Eye Proteins, education, Genetics, Mutation, education.field_of_study, medicine.diagnostic_test, Haplotype, Middle Aged, medicine.disease, Founder Effect, Arabs, Pedigree, Ophthalmoscopy, Phenotype, Haplotypes, Jews, Mutation testing, Female, Visual Fields, Age of onset, Retinitis Pigmentosa, Founder effect
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c99d4f0d7cc90cd726985c4c970d092Test
https://hdl.handle.net/2066/87206Test -
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المؤلفون: Itay Chowers, Alexey Obolensky, Saul Merin, Marilyn D. Farber
المصدر: Journal of Ocular Pharmacology and Therapeutics. 24:80-86
مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Visual acuity, Adolescent, genetic structures, Administration, Topical, medicine.medical_treatment, media_common.quotation_subject, Visual Acuity, Pilot Projects, law.invention, Contrast Sensitivity, Retinal Diseases, Randomized controlled trial, Brimonidine Tartrate, law, Quinoxalines, Ophthalmology, Adrenergic alpha-2 Receptor Agonists, Electroretinography, medicine, Humans, Contrast (vision), Pharmacology (medical), Prospective Studies, Aged, media_common, Pharmacology, Retina, medicine.diagnostic_test, business.industry, Retinal Degeneration, Middle Aged, eye diseases, Artificial tears, Treatment Outcome, medicine.anatomical_structure, Patient Compliance, Female, Visual Fields, medicine.symptom, business, Adrenergic alpha-Agonists, Retinitis Pigmentosa, Retinal Dystrophies
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd71795390cf596c1fb07157bb76ca60Test
https://doi.org/10.1089/jop.2007.0022Test -
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المؤلفون: Dikla Bandah-Rozenfeld, Dror Sharon, Eyal Banin, Dalia Eli, Elia Shevach, Lina Zelinger, Anat Harel, Saul Merin, Avigail Beryozkin, Michal Sagi, Tim Storm
المصدر: Investigative ophthalmologyvisual science. 55(2)
مصطلحات موضوعية: Retinal degeneration, Male, Candidate gene, Genetic Linkage, DNA Mutational Analysis, Single-nucleotide polymorphism, Biology, medicine.disease_cause, Polymorphism, Single Nucleotide, Consanguinity, Retinitis pigmentosa, medicine, Electroretinography, SNP, Humans, Genetic Predisposition to Disease, Israel, Eye Proteins, Gene, Genetics, Mutation, Homozygote, Retinal Degeneration, Chromosome Mapping, medicine.disease, Disease gene identification, eye diseases, Arabs, Pedigree, Jews, Female, Retinitis Pigmentosa
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5f641b6fe3f296afa58d3b774351cb7Test
https://pubmed.ncbi.nlm.nih.gov/24474277Test -
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المؤلفون: Tally Lerman-Sagie, Orly Elpeleg, Saul Merin, Avraham Shaag, Itay Chowers
المصدر: British Journal of Ophthalmology. 83:190-193
مصطلحات موضوعية: Adult, Male, Pathology, medicine.medical_specialty, Mitochondrial DNA, Ataxia, Adolescent, genetic structures, Neurological disorder, DNA, Mitochondrial, Cellular and Molecular Neuroscience, Cone dystrophy, Retinitis pigmentosa, Electroretinography, medicine, Humans, Child, Genetics, business.industry, Point mutation, Dystrophy, Original Articles, Syndrome, medicine.disease, eye diseases, Sensory Systems, Pedigree, Ophthalmology, Female, sense organs, Visual Fields, medicine.symptom, business, Retinitis Pigmentosa, Retinopathy
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f97a76c386cf408ba0e4b02cd1db5c63Test
https://doi.org/10.1136/bjo.83.2.190Test -
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المؤلفون: Val C. Sheffield, Joel Zlotogora, Robert G. Knowlton, Nancy C. Arbour, Edwin M. Stone, Adam B. Kanis, Saul Merin, Tatiana Rokhlina, Ada Rosenmann
المصدر: Human Molecular Genetics. 6:689-694
مصطلحات موضوعية: Genetic Markers, Male, Candidate gene, Achromatopsia, Genetic Linkage, Color Vision Defects, Nerve Tissue Proteins, Iran, Biology, Nystagmus, Pathologic, Gene mapping, Genetics, medicine, Humans, Molecular Biology, Genotyping, Genetics (clinical), Chromosomes, Human, Pair 14, Polymorphism, Genetic, Homozygote, Chromosome Mapping, Chromosome, General Medicine, Disease gene identification, medicine.disease, Founder Effect, eye diseases, Pedigree, Genetic marker, Chromosomes, Human, Pair 2, Jews, Microsatellite, Female
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb6bc915f950b24d0615fa9143185c72Test
https://doi.org/10.1093/hmg/6.5.689Test -
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المؤلفون: Samuel Levinger, Ami Hirsch, Isaac Aizenman, Teunis Bos, Joseph Douieb, David Landau, Saul Merin, Israel Kremer
المصدر: Journal of Cataract and Refractive Surgery. 29:1947-1949
مصطلحات موضوعية: medicine.medical_specialty, Sterilization process, business.industry, medicine.medical_treatment, technology, industry, and agriculture, food and beverages, LASIK, Keratomileusis, medicine.disease, Sensory Systems, Surgery, Ophthalmology, stomatognathic system, Refractive surgery, Microkeratome, medicine, sense organs, business, Diffuse lamellar keratitis
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::b87465775d267438a0cdddcad0bad83aTest
https://doi.org/10.1016/j.jcrs.2003.07.001Test