المؤلفون: Inbal Hershco, Michael Fry, Pnina Weisman-Shomer, Lawrence A. Loeb, Samer Khateb

المصدر: Nucleic Acids Research. 32:4145-4154

مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, GTP', Heterogeneous Nuclear Ribonucleoprotein A1, RNA Stability, Amino Acid Motifs, Molecular Sequence Data, Protein domain, Nerve Tissue Proteins, RNA-binding protein, Guanosine triphosphate, Biology, Conserved sequence, Fragile X Mental Retardation Protein, chemistry.chemical_compound, Adenosine Triphosphate, Protein structure, Heterogeneous-Nuclear Ribonucleoprotein Group A-B, Genetics, Amino Acid Sequence, Binding site, Conserved Sequence, Repetitive Sequences, Nucleic Acid, Binding Sites, Sequence Homology, Amino Acid, RNA-Binding Proteins, DNA, Articles, Molecular biology, Protein Structure, Tertiary, nervous system diseases, G-Quadruplexes, chemistry, Nucleic Acid Conformation, RNA, Guanosine Triphosphate

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54b3e13f6c1b128ac97f8f35e5cfb3dfTest
https://doi.org/10.1093/nar/gkh745Test

المؤلفون: Menachem Gross, Liliana Mizrahi-Meissonnier, Uri Laxer, Eyal Banin, Robert K. Koenekoop, Dror Sharon, Lina Zelinger, Samer Khateb, Carmen Ayuso

المصدر: Journal of medical genetics. 51(7)

مصطلحات موضوعية: Male, Heterozygote, Usher syndrome, media_common.quotation_subject, Nonsense, Nonsense mutation, DNA Mutational Analysis, Cell Cycle Proteins, Biology, Autoantigens, Polymorphism, Single Nucleotide, Consanguinity, Retinitis pigmentosa, otorhinolaryngologic diseases, Genetics, medicine, Humans, Genetic Predisposition to Disease, Eye Proteins, Genetics (clinical), Exome sequencing, Phylogeny, media_common, Base Sequence, Homozygote, medicine.disease, Disease gene identification, Pedigree, Codon, Nonsense, Mutation (genetic algorithm), Sensorineural hearing loss, Female, Usher Syndromes, Genome-Wide Association Study

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4ec7f5b1b81a12315593b156bb263abTest
https://pubmed.ncbi.nlm.nih.gov/24780881Test

المؤلفون: Samer Khateb, Itay Chowers

المصدر: Encyclopedia of Ophthalmology ISBN: 9783642359514

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::a3e52cc9adabe3205cb8efa0eec7ab25Test
https://doi.org/10.1007/978-3-642-35951-4_326-4Test

المؤلفون: Pnina Weisman-Shomer, Michael Fry, Eyal Bengal, Shulamit Etzioni, Anat Yafe, Samer Khateb

المصدر: The Journal of biological chemistry. 280(29)

مصطلحات موضوعية: Transcriptional Activation, Transcription, Genetic, Muscle Proteins, Biology, MyoD, G-quadruplex, Biochemistry, E-Box Elements, chemistry.chemical_compound, Transcription (biology), Basic Helix-Loop-Helix Transcription Factors, Animals, Humans, Enhancer, Molecular Biology, Transcription factor, MyoD Protein, Cell Biology, DNA, DNA-Binding Proteins, G-Quadruplexes, chemistry, Regulatory sequence, Biophysics, Nucleic Acid Conformation, Dimerization, Protein Binding, Transcription Factors

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a058a97c8571dcafb6a7a9e64399cefTest
https://pubmed.ncbi.nlm.nih.gov/15923190Test

المؤلفون: Pnina Weisman-Shomer, Michael Fry, Samer Khateb, Orit Wolfovitz-Barchad, Inbal Hershco, Esther Cohen, Laurence H. Hurley

مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, Porphyrins, Oligonucleotides, RNA-binding protein, Nerve Tissue Proteins, Biology, Nucleic Acid Denaturation, DNA-binding protein, Binding, Competitive, chemistry.chemical_compound, Exon, Fragile X Mental Retardation Protein, Transcription (biology), Genetics, Oligonucleotide, Temperature, RNA-Binding Proteins, Articles, DNA, DNA Methylation, Molecular biology, FMR1, nervous system diseases, DNA-Binding Proteins, Repressor Proteins, Kinetics, chemistry, Nucleic Acid Conformation, Trinucleotide repeat expansion, Trinucleotide Repeat Expansion

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ace67daf84763b6c588e335d50a83596Test
https://europepmc.org/articles/PMC165968Test/

المؤلفون: Ksenya Cohen-katsenelson, Tanya Wasserman, Samer Khateb, Alan J. Whitmarsh, Ami Aronheim

المساهمون: The Pennsylvania State University CiteSeerX Archives

المصدر: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3462610/pdf/bj4390381.pdfTest.

وصف الملف: application/pdf

العلاقة: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.668.4145Test; http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3462610/pdf/bj4390381.pdfTest

الإتاحة: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3462610/pdf/bj4390381.pdfTest

المؤلفون: Ornit Crystal-Shalit, Lina Zelinger, Dror Sharon, Tamar Ben-Yosef, Menachem Gross, Saul Merin, Samer Khateb, Eyal Banin

المصدر: PLoS ONE
PLoS ONE, Vol 7, Iss 12, p e51566 (2012)

مصطلحات موضوعية: Male, Genetic Screens, DNA Mutational Analysis, lcsh:Medicine, Cell Cycle Proteins, Autosomal Recessive, Chromosome Segregation, Exome, Age of Onset, Israel, lcsh:Science, Frameshift Mutation, Exome sequencing, Genetics, Multidisciplinary, Homozygote, Exons, Disease gene identification, Founder Effect, Pedigree, Phenotype, Medicine, Retinal Disorders, Female, Sensorineural hearing loss, medicine.symptom, Sequence Analysis, Retinitis Pigmentosa, Research Article, Hearing loss, Molecular Sequence Data, Genes, Recessive, Biology, Polymorphism, Single Nucleotide, Frameshift mutation, Audiometry, Retinitis pigmentosa, otorhinolaryngologic diseases, medicine, Humans, Hearing Loss, Adaptor Proteins, Signal Transducing, Clinical Genetics, Base Sequence, Genome, Human, lcsh:R, Computational Biology, Sequence Analysis, DNA, medicine.disease, Ophthalmology, Alternative Splicing, Cytoskeletal Proteins, Genetics of Disease, Genetic Polymorphism, lcsh:Q, Population Genetics, Founder effect

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a841674b2e3680c8f9e7fe50bcdd6cf1Test
https://doi.org/10.1371/journal.pone.0051566Test

المؤلفون: Ksenya Cohen‑Katsenelson, Tanya Wasserman, Samer Khateb, Alan J. Whitmarsh, Ami Aronheim

المصدر: Biochemical Journal; Nov2011, Vol. 439 Issue 3, p381-390, 10p

مصطلحات موضوعية: SCAFFOLD proteins, MITOGEN-activated protein kinases, CELLULAR signal transduction, PROTEIN structure, PROTEIN binding, MOLECULAR biology, PROTEIN-protein interactions