-
1دورية أكاديمية
المؤلفون: Tayybeh Khamar, Mehrnaz Narooie-Nejad, Leila Kordi, Farahnaz Farzaneh
المصدر: Crescent Journal of Medical and Biological Sciences, Vol 7, Iss 4, Pp 560-563 (2020)
مصطلحات موضوعية: sperm dna fragmentation index, dfi, infertility, semen analysis, male factor, Medicine
وصف الملف: electronic resource
-
2
المؤلفون: Nickie Stangel, Yongwook Dan, Conceição Egas, Terri L. Young, Kristina N. Whisenhunt, Jacob S Martin, Fatemeh Suri, Reza Maroofian, Samuel J Huang, Susana Carmona, Susan E. Quaggin, Tomokazu Souma, Emmanuelle Souzeau, Behzad Fallahi Motlagh, Jing Jin, Sarah M LaMartina, Nicole M Jody, Brendan M Lawson, Mehrnaz Narooie-Nejad, Heather D. Potter, Emily C. Higuchi, Owen M. Siggs, Jamie E Craig, Eduardo Silva, Vachiranee Limviphuvadh, Sebastian Maurer-Stroh, Xue Zhang, Elahe Elahi, Yasmin S. Bradfield, Maria José Simões, Evie Anagnos, Sean Martin, Stuart W. Tompson
المصدر: Investigative Ophthalmology & Visual Science
مصطلحات موضوعية: 0301 basic medicine, Male, Pathology, genetic structures, Genotyping Techniques, Glaucoma, Penetrance, Mice, 0302 clinical medicine, Gene Frequency, Missense mutation, Protein Isoforms, Phosphorylation, Exome sequencing, Middle Aged, Receptor, TIE-2, Pedigree, Schlemm's canal, Child, Preschool, Female, Haploinsufficiency, medicine.medical_specialty, Blotting, Western, Mutation, Missense, Biology, 03 medical and health sciences, Dysgenesis, Exome Sequencing, medicine, Genetics, Human Umbilical Vein Endothelial Cells, Animals, Humans, Allele, Allele frequency, SVEP1, Intraocular Pressure, Aged, modifier, Genes, Modifier, Hydrophthalmos, Infant, Newborn, Infant, medicine.disease, 030104 developmental biology, glaucoma, HEK293 Cells, TEK, 030221 ophthalmology & optometry, Cell Adhesion Molecules
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b98fc5b18cd56f614b4b1c8935f903e8
http://europepmc.org/articles/PMC7545080 -
3
المؤلفون: Mehrnaz Narooie-Nejad, Maryam Moossavi, Milad Mohammadoo-Khorasani, Danial Jahantigh, Mahdieh Mousavi, Ali Moghtaderi, Saeedeh Salimi
المصدر: Russian Journal of Genetics. 53:147-152
مصطلحات موضوعية: 0301 basic medicine, Genetics, biology, Multiple sclerosis, medicine.disease, Human genetics, law.invention, Genotype frequency, 03 medical and health sciences, 030104 developmental biology, law, biology.protein, medicine, Gene polymorphism, Allele, Gene, Polymerase chain reaction, Polymerase
-
4
المصدر: Biomedical Reports. 6:108-112
مصطلحات موضوعية: 0301 basic medicine, Autoimmune disease, General Neuroscience, Thyroid, Single-nucleotide polymorphism, Articles, General Medicine, Biology, medicine.disease, General Biochemistry, Genetics and Molecular Biology, Thyroiditis, 03 medical and health sciences, 030104 developmental biology, 0302 clinical medicine, medicine.anatomical_structure, 030220 oncology & carcinogenesis, Immunology, Genotype, medicine, Cytotoxic T cell, General Pharmacology, Toxicology and Pharmaceutics, Genotyping, Allele frequency
-
5
المؤلفون: Saeid Sadabadi, Susan Banihashemi, Hossein Darvish, Peyman Jamali, Hassan Farbod Mofidi Tehrani, Hossein Najmabadi, Javad Jamshidi, Abbas Tafakhori, Farkhondeh Behjati, Mehrnaz Narooie-Nejad, Hamid Ghaedi, Hossein Dehghani, Saghar Ghasemi Firouzabadi, Roxana Kariminejad, Mahboubeh Firouzkouhi Moghaddam, Roshanak Vameghi
المصدر: Molecular Neurobiology. 54:7019-7027
مصطلحات موضوعية: 0301 basic medicine, Candidate gene, DNA Copy Number Variations, Neuroscience (miscellaneous), Biology, Bioinformatics, 03 medical and health sciences, Cellular and Molecular Neuroscience, Neurodevelopmental disorder, Gene Duplication, mental disorders, Intellectual disability, Gene duplication, medicine, Humans, Heritability of autism, Copy-number variation, Autistic Disorder, Genetics, Syndrome, medicine.disease, 030104 developmental biology, Neurology, Receptors, Vasoactive Intestinal Peptide, Type II, Autism, VIPR2
-
6
المؤلفون: Saeedeh Salimi, Omid Taji, Mohammad Hormozi, Ava Rasouli, Fateme Zarei, Mehrnaz Narooie-Nejad
المصدر: Gene, Cell and Tissue.
مصطلحات موضوعية: Genetics, TPH2, business.industry, medicine.disease, Hypomania, Polymorphism (computer science), Genotype, medicine, Bipolar disorder, medicine.symptom, Allele, business, Mania, Allele frequency
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::09f37ce6b53c936f15b26765c385ca2b
https://doi.org/10.5812/gct.86109 -
7
المؤلفون: Mehrnaz Narooie-Nejad, Saeedeh Salimi, Hosein Moghadam, Mahmoud Ali Kaykhaei, Soroosh Dabiri, Danial Jahantigh, Dor Mohammad Kordi Tamandani, Ava Rasouli
المصدر: Meta Gene. 24:100693
مصطلحات موضوعية: 0301 basic medicine, Genetics, chemical and pharmacologic phenomena, Biology, medicine.disease, Thyroiditis, PTPN22, 03 medical and health sciences, 030104 developmental biology, 0302 clinical medicine, 030220 oncology & carcinogenesis, Genotype, medicine, CTLA4 Gene, Gene polymorphism, Allele, Gene, Allele frequency, Genetics (clinical)
-
8
المؤلفون: Mehrnaz Narooie-Nejad
المصدر: Gene, Cell and Tissue. 5
مصطلحات موضوعية: medicine.medical_specialty, Intraocular pressure, genetic structures, business.industry, Glaucoma, Disease, Gene mutation, medicine.disease, eye diseases, Genetic linkage, Ophthalmology, medicine, Optic nerve, Eye disorder, sense organs, Age of onset, business
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::d3054a85872e683f62996cd72fe0c092
https://doi.org/10.5812/gct.74203 -
9
المؤلفون: Golbarg Talebian, Saeedeh Salimi, Farzaneh Farajian-Mashhadi, Mehrnaz Narooie-Nejad, Roya Alavi-Naini
المصدر: Biomedical Reports. 3:189-194
مصطلحات موضوعية: Genetics, integumentary system, business.industry, General Neuroscience, Haplotype, Case-control study, Articles, macromolecular substances, General Medicine, environment and public health, Genetic analysis, Calcitriol receptor, General Biochemistry, Genetics and Molecular Biology, law.invention, law, Immunology, Genotype, Medicine, General Pharmacology, Toxicology and Pharmaceutics, Restriction fragment length polymorphism, Allele, business, Polymerase chain reaction
-
10
المؤلفون: Brandy Klotzle, Iman Safari, Hamidreza Moazzeni, Jian-Bing Fan, Elahe Elahi, Mehrnaz Narooie-Nejad, Fatemeh Suri, Mohammad-Reza Rohani, Ali Khajeh
المصدر: Journal of the Neurological Sciences. 347:305-309
مصطلحات موضوعية: Adult, Male, Heterozygote, Adolescent, Turkey, Cystathionine beta-Synthase, Homocystinuria, Bioinformatics, Polymorphism, Single Nucleotide, Young Adult, Intellectual Disability, Intellectual disability, medicine, Humans, SNP, Genetic Predisposition to Disease, Allele, Genetics, biology, Genetic heterogeneity, Homozygote, medicine.disease, Disease gene identification, Cystathionine beta synthase, Neurology, Mutation, Mutation (genetic algorithm), biology.protein, Female, Neurology (clinical)