المؤلفون: Niloofar Bazazzadegan, Marzieh Dehghan Shasaltaneh, Kioomars Saliminejad, Koorosh Kamali, Mehdi Banan, Reza Nazari, Gholam Hossein Riazi, Hamid Reza Khorram Khorshid

المصدر: Advanced Pharmaceutical Bulletin, Vol 7, Iss 4, Pp 629-636 (2017)

مصطلحات موضوعية: Sporadic Alzheimer disease, Ectoine, Gene expression, Morris Water Maze test, STZ- rat model, Therapeutics. Pharmacology, RM1-950

وصف الملف: electronic resource

Relation: http://apb.tbzmed.ac.ir/PDF/apb-7-629.pdf; https://doaj.org/toc/2228-5881; https://doaj.org/toc/2251-7308

URL الوصول: https://doaj.org/article/bc03bad2f71349d28d5f39a29ccc17f4

المؤلفون: Niloofar Bazazzadegan, Marzieh Dehghan Shasaltaneh, Kioomars Saliminejad, Koorosh Kamali, Mehdi Banan, Hamid Reza Khorram Khorshid

المصدر: Advanced Pharmaceutical Bulletin, Vol 7, Iss 3, Pp 491-494 (2017)

مصطلحات موضوعية: Alzheimer’s disease, Gene expression, Herbal extract, Rat model, Therapeutics. Pharmacology, RM1-950

وصف الملف: electronic resource

Relation: http://journals.tbzmed.ac.ir/APB/Manuscript/APB-7-491.pdf; https://doaj.org/toc/2228-5881; https://doaj.org/toc/2251-7308

URL الوصول: https://doaj.org/article/dac0240b61a54b7f8110730f89fe301e

المؤلفون: Niloofar BAZAZZADEGAN, Raheleh VAZEHAN, Mahsa FADAEE, Zohreh FATTAHI, Ayda ABOLHASSANI, Elham PARSIMEHR, Zahra KALHOR, Mehrshid FARAJI ZONOOZ, Fatemeh AHANGARI, Shima DEHDAHSI, Farshide SAMIEE, Payman JAMALI, Haleh HABIBI, Younes NOURIZADEH, Shokouh MAHDAVI, Maryam BEHESHTIAN, Ariana KARIMINEJAD, Richard JH SMITH, Hossein NAJMABADI

المصدر: Iranian Journal of Public Health, Vol 48, Iss 10 (2019)

مصطلحات موضوعية: OtoSCOPE, Hereditary hearing loss, Novel variant, Known variant, Public aspects of medicine, RA1-1270

وصف الملف: electronic resource

Relation: https://ijph.tums.ac.ir/index.php/ijph/article/view/18556; https://doaj.org/toc/2251-6085; https://doaj.org/toc/2251-6093

URL الوصول: https://doaj.org/article/2bb2e364df144354b6a117fcf7751f96

المؤلفون: Nazanin Esmaeili Anvar, Niloofar Bazazzadegan, Mina Ohadi, Kourosh Kamali, Hamidreza Khorram Khorshid

المصدر: Sālmand, Vol 11, Iss 1, Pp 64-71 (2016)

مصطلحات موضوعية: Cardiovascular, Alzheimer, Polymorphisms, Cytokines, Interleukin 16, Geriatrics, RC952-954.6, Public aspects of medicine, RA1-1270

وصف الملف: electronic resource

Relation: http://salmandj.uswr.ac.ir/browse.php?a_code=A-10-1187-2&slc_lang=en&sid=1; https://doaj.org/toc/1735-806X

URL الوصول: https://doaj.org/article/6f2d7462335b4251b06e4761f872f5f3

المؤلفون: Kimia Kahrizi, Mahsa Fadaee, Zohreh Fattahi, Maryam Beheshtian, Shahrouz Khoshbakht, Raheleh Vazehan, Ayda Abolhassani, Arzu Celik, Ariana Kariminejad, Mina Makvand, Mehrshid Faraji Zonooz, Hossein Najmabadi, Niloofar Bazazzadegan, Elham Parsimehr

المصدر: Archives of Iranian Medicine. 24:364-373

مصطلحات موضوعية: Genetics, medicine.diagnostic_test, Cilium, General Medicine, Biology, medicine.disease, Phenotype, Ciliopathies, Western blot, Intellectual disability, medicine, Exome, Gene, Exome sequencing

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::99ec8ad2418c63b130aec48380891b01
https://doi.org/10.34172/aim.2021.53

المؤلفون: Seyedeh Sedigheh Abedini, Niloofar Bazazzadegan, Mandana Hasanzad

المصدر: Precision Medicine in Clinical Practice ISBN: 9789811950810

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::9bb22430f404d6816bd978a3b88c2432
https://doi.org/10.1007/978-981-19-5082-7_8

المؤلفون: Marzieh Mohseni, Kevin T. Booth, Atefeh Khoshaeen, Fatemeh Bahrami, Payman Jamali, Hossein Najmabadi, Niloofar Bazazzadegan, Kimia Kahrizi, Nooshin Nikzat, Farkhonde Habibi, Richard J.H. Smith, Fariba Ardalani, Mojgan Babanejad, Hanieh Behravan, Fatemeh Keshavarzi, Michael Nothnagel, Faezeh Jahanshad, Seyed Morteza Seifati, Fatemeh Ghodratpour, Sanaz Arzhangi, Behzad Davarnia, Zohreh Mehrjoo, Holger Thiele, Khadijeh Jalalvand, Maryam Beheshtian, Hela Azaiez, Sepide Mirzaei, Hasan Otukesh

المصدر: Clin Genet

مصطلحات موضوعية: 0301 basic medicine, Adult, Male, Candidate gene, Adolescent, Hearing loss, Consanguinity, 030105 genetics & heredity, Biology, Iran, DNA sequencing, Article, Cohort Studies, 03 medical and health sciences, Young Adult, Locus heterogeneity, Exome Sequencing, Genetics, medicine, Humans, Exome, Genetic Predisposition to Disease, Child, Hearing Loss, Gene, Genetics (clinical), Exome sequencing, Genetic heterogeneity, High-Throughput Nucleotide Sequencing, Middle Aged, medicine.disease, Pedigree, 030104 developmental biology, Child, Preschool, Mutation, Female, medicine.symptom

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca2652aadda21337130620b09922d67a
https://europepmc.org/articles/PMC8195868/

المؤلفون: Seyed Morteza Seifati, Maryam Beheshtian, Kevin T. Booth, Behzad Davarnia, Faezeh Jahanshad, Farkhonde Habibi, Michael Nothnagel, Atefeh Khoshaeen, Hanieh Behravan, K. Kahrizi, Fatemeh Ghodratpour, Sanaz Arzhangi, Fatemeh Bahrami, Hossein Najmabadi, Payman Jamali, Marzieh Mohseni, Fariba Ardalani, Mojgan Babanejad, Khadijeh Jalalvand, Hela Azaiez, Sepide Mirzaei, Holger Thiele, Zohreh Mehrjoo, Hasan Otukesh, Nooshin Nikzat, Richard J.H. Smith, Fatemeh Keshavarzi, Niloofar Bazazzadegan

مصطلحات موضوعية: Novel gene, Hearing loss, medicine, Computational biology, Biology, medicine.symptom, Exome sequencing

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c907ed7b80c8ef2500764b3b5e3a683f
https://doi.org/10.1111/cge.13956/v4/response1

المؤلفون: Kimia Kahrizi, Zohreh Fattahi, Hossein Najmabadi, Maryam Rahimi, Hans-Hilger Ropers, Arzu Celik, Masoumeh Hosseini, Ibrahim Ihsan Taskiran, Somayeh Kazeminasab, Morteza Oladnabi, Mohammad Haddadi, Niloofar Bazazzadegan

المصدر: American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 177:691-699

مصطلحات موضوعية: 0301 basic medicine, Genetics, MAPK/ERK pathway, Kinase, Cell migration, Biology, Receptor tyrosine kinase, Frameshift mutation, 03 medical and health sciences, Cellular and Molecular Neuroscience, Psychiatry and Mental health, 030104 developmental biology, 0302 clinical medicine, biology.protein, CNKSR1 Gene, Enhancer, Protein kinase A, 030217 neurology & neurosurgery, Genetics (clinical)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::6c288a34a8334a01bbcc3b93cda31f47
https://doi.org/10.1002/ajmg.b.32648

المؤلفون: mitra Sapahvand, kimia Kahrizi, ahmad Daneshi, marziye Mohseni, yaser Riazalhosseini, niloofar Bazazzadegan, hosein Najmabadi

المصدر: Yafteh, Vol 8, Iss 2, Pp 89-95 (2007)

مصطلحات موضوعية: Autosomal recessive non-syndromic hearing loss (ARNSHL), GJB2, 35delG, Medicine, Medicine (General), R5-920

Relation: http://yafte.lums.ac.ir/browse.php?a_code=A-10-1-312&slc_lang=en&sid=1; https://doaj.org/toc/1563-0773; https://doaj.org/article/22a432b565cb44e8a380a2017a43d964

الاتاحة: https://doaj.org/article/22a432b565cb44e8a380a2017a43d964

المؤلفون: Hamid Reza Khorram Khorshid, Koorosh Kamali, Niloofar Bazazzadegan, Marzieh Dehghan Shasaltaneh, Kioomars Saliminejad, Mehdi Banan

المصدر: Advanced Pharmaceutical Bulletin, Vol 7, Iss 3, Pp 491-494 (2017)
Advanced Pharmaceutical Bulletin

مصطلحات موضوعية: 0301 basic medicine, Pathology, medicine.medical_specialty, Short Communication, Pharmaceutical Science, Morris water navigation task, Hippocampus, Inflammation, 010501 environmental sciences, Pharmacology, medicine.disease_cause, 01 natural sciences, Neuroprotection, 03 medical and health sciences, Death-associated protein 6, Gene expression, medicine, General Pharmacology, Toxicology and Pharmaceutics, 0105 earth and related environmental sciences, 030102 biochemistry & molecular biology, business.industry, lcsh:RM1-950, Streptozotocin, lcsh:Therapeutics. Pharmacology, Herbal extract, Rat model, medicine.symptom, business, Alzheimer’s disease, Oxidative stress, medicine.drug

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7398096fb1acd5c83c0918255be2fe9
http://journals.tbzmed.ac.ir/APB/Manuscript/APB-7-491.pdf

المؤلفون: Hossein Najmabadi, Marzieh Mohseni, Niloofar Bazazzadegan, Kimia Kahrizi, Sanaz Arzhangi, Mojgan Babanejad, Masoud Motasaddi Zarandy, Nooshin Nikzat

المصدر: International journal of pediatric otorhinolaryngology. 126

مصطلحات موضوعية: Male, medicine.medical_specialty, Heterozygote, Adolescent, Hearing loss, Hearing Loss, Sensorineural, Iran, Connexins, 03 medical and health sciences, Gjb2 gene, Consanguinity, 0302 clinical medicine, Keratoderma, Palmoplantar, 030225 pediatrics, otorhinolaryngologic diseases, medicine, Humans, 030223 otorhinolaryngology, business.industry, De novo mutation, General Medicine, Sequence Analysis, DNA, medicine.disease, Dermatology, Pedigree, Connexin 26, Palmoplantar keratoderma, Otorhinolaryngology, Pediatrics, Perinatology and Child Health, Mutation (genetic algorithm), Mutation, Sensorineural hearing loss, Female, medicine.symptom, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7238427478cb31802cbd5364291a144d
https://pubmed.ncbi.nlm.nih.gov/31785923

المؤلفون: Somayeh, Kazeminasab, Ibrahim Ihsan, Taskiran, Zohreh, Fattahi, Niloofar, Bazazzadegan, Masoumeh, Hosseini, Maryam, Rahimi, Morteza, Oladnabi, Mohammad, Haddadi, Arzu, Celik, Hans-Hilger, Ropers, Hossein, Najmabadi, Kimia, Kahrizi

المصدر: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics. 177(8)

مصطلحات موضوعية: Adult, Male, Adolescent, MAP Kinase Signaling System, Intracellular Signaling Peptides and Proteins, Brain, High-Throughput Nucleotide Sequencing, Genes, Recessive, Syndrome, Iran, Pedigree, Drosophila melanogaster, Intellectual Disability, Mutation, Animals, Drosophila Proteins, Humans, Family, Female, Adaptor Proteins, Signal Transducing, Signal Transduction

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::4199a3affc3537eb5b4c1659336aeafd
https://pubmed.ncbi.nlm.nih.gov/30450701

المؤلفون: Nooshin Nikzat, Kevin T. Booth, Richard J.H. Smith, Allen C. Simpson, Kimia Kahrizi, Maryam Beheshtian, Reza Mozafari, Fariba Ardalani, Mojgan Babanejad, Farahnaz Sabbagh, Kathy L. Frees, Nicole C. Meyer, Leila Jamali, Zohreh Mehrjoo, Niloofar Bazazzadegan, Sanaz Arzhangi, Hossein Khodaei, Christina M. Sloan-Heggen, Tara Akhtarkhavari, Maryam Taghdiri, Hela Azaiez, Mohammad Farhadi, Marzieh Mohseni, Hasan Otukesh, Seyed Morteza Seifati, Hossein Najmabadi, Saeideh Vaziri, Ahmad Daneshi

المصدر: Journal of Medical Genetics. 52:823-829

مصطلحات موضوعية: MYO15A, medicine.medical_specialty, Hearing loss, Genes, Recessive, Consanguinity, Iran, Biology, Connexins, Article, Gene Frequency, Molecular genetics, otorhinolaryngologic diseases, Genetics, medicine, Humans, Genetic Predisposition to Disease, Hearing Loss, Genetic Association Studies, Genetics (clinical), Massive parallel sequencing, Genetic heterogeneity, Founder Effect, Connexin 26, Medical genetics, medicine.symptom, Founder effect

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::73e2cc709ef1b865779bf39e22505b6b
https://doi.org/10.1136/jmedgenet-2015-103389

المؤلفون: Niloofar, Bazazzadegan, Marzieh, Dehghan Shasaltaneh, Kioomars, Saliminejad, Koorosh, Kamali, Mehdi, Banan, Hamid Reza, Khorram Khorshid

المصدر: Avicenna Journal of Medical Biotechnology

مصطلحات موضوعية: Original Article, Gene expression, Alzheimer disease, Herbal medicine

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::3022e431e1d024f3f03bca2220c07abd
https://pubmed.ncbi.nlm.nih.gov/28706608

المؤلفون: Todd E. Scheetz, Marta L. Tamayo, Thomas L. Casavant, Josef Ekstein, Sean S. Ephraim, E. Ann Black-Ziegelbein, Scott Happe, Kimia Kahrizi, Richard J.H. Smith, A. Giuffre, Shin-ichi Usami, Hela Azaiez, Allen C. Simpson, Kevin T. Booth, Terry A. Braun, Tao Yang, Michael S. Hildebrand, Hossein Najmabadi, Niloofar Bazazzadegan, Mehmet Emin Erdal, Irene Gazquez, A. Eliot Shearer, Swati Joshi, Harini Ravi, Nancy Gelvez, Yıldırım Ahmet Bayazıt, Greizy López Leal, Chaim Jalas, Jose Gurrola, Emily M LeProust, Robert W. Eppsteiner, Jose A. Lopez-Escamez

المصدر: American journal of human genetics, vol 95, iss 4

مصطلحات موضوعية: dbSNP, Evolution, Genome-wide association study, Biology, Medical and Health Sciences, Connexins, Evolution, Molecular, Gene Frequency, Clinical Research, Report, Ethnicity, Genetics, medicine, 2.1 Biological and endogenous factors, Humans, Exome, Genetics(clinical), Aetiology, Ethnic-Specific Differences, 1000 Genomes Project, Hearing Loss, Allele frequency, Phylogeny, Genetics (clinical), Genetic testing, Genetics & Heredity, Genome, Massive parallel sequencing, medicine.diagnostic_test, Genome, Human, Human Genome, Molecular, Minor Allele Frequency, Genetic Variation, Biological Sciences, Connexin 26, Minor allele frequency, Case-Control Studies, Pathogenic Deafness Variants, Human, Genome-Wide Association Study

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb7b535ca2596b6aef410ec089b2b89c
https://doi.org/10.1016/j.ajhg.2014.09.001

المؤلفون: Maryam, Beheshtian, Mojgan, Babanejad, Hela, Azaiez, Niloofar, Bazazzadegan, Diana, Kolbe, Christina, Sloan-Heggen, Sanaz, Arzhangi, Kevin, Booth, Marzieh, Mohseni, Kathy, Frees, Mohammad Hossein, Azizi, Ahmad, Daneshi, Mohammad, Farhadi, Kimia, Kahrizi, Richard Jh, Smith, Hossein, Najmabadi

المصدر: Archives of Iranian medicine. 19(10)

مصطلحات موضوعية: Hearing Loss, Sensorineural, Membrane Transport Proteins, Iran, Myosins, Connexins, Article, Connexin 26, Consanguinity, Sulfate Transporters, Myosin VIIa, Mutation, otorhinolaryngologic diseases, Humans, Genetic Testing, Delivery of Health Care

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::07d4468617125ac00e26546749353b24
https://pubmed.ncbi.nlm.nih.gov/27743438

المؤلفون: Hossein Najmabadi, Amin Najmabadi, Elahe Sohrabi, Mojgan Babanejad, Niloofar Bazazzadegan, Zohreh Fattahi, Nicole C. Meyer, Peyman Jamali, Carla Nishimura, Kimia Kahrizi, Nooshin Nikzat, Richard J.H. Smith, Farkhonde Habibi

المصدر: American Journal of Medical Genetics Part A. :2485-2492

مصطلحات موضوعية: Hearing loss, Hearing Loss, Sensorineural, Genes, Recessive, Locus (genetics), Iran, Biology, Connexins, Gjb2 gene, otorhinolaryngologic diseases, Genetics, medicine, Humans, Family, Nonsyndromic deafness, Gene, Genetics (clinical), Homozygote, Chromosome Mapping, medicine.disease, Disease gene identification, Phenotype, Genetic load, Connexin 26, Mutation, medicine.symptom, Microsatellite Repeats

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0267742015add5cf30484ff9693ba808
https://doi.org/10.1002/ajmg.a.35572

المؤلفون: Farahnaz Sabbagh Kermani, Hossein Najmabadi, Narges Nouri, Atie Kashef, Shima Sahraian, Atefeh Khoshaeen, Faezeh Mojahedi, Mojgan Babanejad, Niloofar Bazazzadegan, Maryam Taghdiri, Kimia Kahrizi, Batool Azadeh, Payman Jamali, Hilda Yazdan, Richard J.H. Smith, Haleh Habibi, Zohreh Fattahi, Nicole C. Meyer, Farahnaz Reyhanifar, Nooshin Nikzat, Carla Nishimura

المصدر: International Journal of Pediatric Otorhinolaryngology. 76:1164-1174

مصطلحات موضوعية: Proband, Hearing loss, DNA Mutational Analysis, Population, Locus (genetics), Consanguinity, Iran, Connexins, Exon, Prevalence, otorhinolaryngologic diseases, Humans, Medicine, Allele, Hearing Loss, education, Genetics, education.field_of_study, Polymorphism, Genetic, business.industry, General Medicine, Cline (biology), Connexin 26, Otorhinolaryngology, Mutation, Pediatrics, Perinatology and Child Health, medicine.symptom, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9c0e2aeb3e8d0791170edd0a07206dc
https://doi.org/10.1016/j.ijporl.2012.04.026

المؤلفون: Hossein Najmabadi, A. Eliot Shearer, Kimia Kahrizi, Zohreh Fattahi, Seyed Navid Almadani, Sanaz Arzhangi, Batool Azadeh, Richard J.H. Smith, Niloofar Bazazzadegan, Mojgan Babanejad, Fatemehsadat Esteghamat, Khadijeh Jalalvand, Nooshin Nikzat, Rezvan Abtahi

المصدر: American Journal of Medical Genetics Part A. :1857-1864

مصطلحات موضوعية: Male, MYO15A, Population, Nonsense mutation, Genes, Recessive, Locus (genetics), Deafness, Iran, Myosins, Gene mutation, Biology, Article, Connexins, Genetic linkage, otorhinolaryngologic diseases, Genetics, Humans, Missense mutation, Mutation frequency, education, Genetics (clinical), education.field_of_study, Chromosome Mapping, Molecular biology, Pedigree, Connexin 26, Mutation, Female, Chromosomes, Human, Pair 17

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e84d6481b8539325e1667c4bf9e0c2d8
https://doi.org/10.1002/ajmg.a.34411