المؤلفون: Mohammadreza Hajjari, Iman Sadeghi, Abbas Salavaty, Habib Nasiri, Maryam Tahmasebi Birgani

المصدر: Genomics & Informatics, Vol 14, Iss 4, Pp 234-240 (2016)

مصطلحات موضوعية: apoptosis, codon, gene expression regulation, translation, Genetics, QH426-470

وصف الملف: electronic resource

Relation: http://genominfo.org/upload/pdf/gni-14-234.pdf; https://doaj.org/toc/1598-866X; https://doaj.org/toc/2234-0742

URL الوصول: https://doaj.org/article/c19223cd49bc473fb6c37ec3eb51dcf3

المؤلفون: Habib Nasiri, Jila Dastan, Mohammad Hasan Seifi, Noori Dalooi, Saeed Reza Ghaffari

المصدر: Journal of Family and Reproductive Health, Vol 3, Iss 2 (2009)

مصطلحات موضوعية: Prenatal diagnosis, Chromosomal aberration, Short tandem repeat, Heterozygosity, Iranian population, Gynecology and obstetrics, RG1-991

وصف الملف: electronic resource

Relation: https://jfrh.tums.ac.ir/index.php/jfrh/article/view/66; https://doaj.org/toc/1735-8949; https://doaj.org/toc/1735-9392

URL الوصول: https://doaj.org/article/a4225d0fd84744aaa1395e4a45171b0c

المؤلفون: Mina Izadyar, Jila Dastan, Tayebeh Sabokbar, Solmaz Shoraka, Azadeh Shojaei, Habib Nasiri, Saeed Reza Ghaffari

المصدر: Journal of Family and Reproductive Health, Vol 1, Iss 2 (2007)

مصطلحات موضوعية: Carrier detection, RBC indices, HbA2, Mutation analysis, Gynecology and obstetrics, RG1-991

وصف الملف: electronic resource

Relation: https://jfrh.tums.ac.ir/index.php/jfrh/article/view/18; https://doaj.org/toc/1735-8949; https://doaj.org/toc/1735-9392

URL الوصول: https://doaj.org/article/fe14f2873e204a3287457477ad2dd82f

المؤلفون: Mandana Mahmoodi, Hossein Ansari, Javad Mohammadi-Asl, Habib Nasiri, Mohammadreza Hajjari, Maryam Tahmasebi-Birgani, Abolghasem Kollaee

المصدر: Gene. 708:10-13

مصطلحات موضوعية: Male, 0301 basic medicine, medicine.medical_specialty, dbSNP, Iran, Biology, DNA sequencing, Mitochondrial Proteins, Consanguinity, 03 medical and health sciences, 0302 clinical medicine, Exome Sequencing, Genetics, medicine, Humans, Spinocerebellar Ataxias, Exome sequencing, Sequence Deletion, Homozygote, High-Throughput Nucleotide Sequencing, Autosomal recessive cerebellar ataxia, General Medicine, medicine.disease, Pedigree, 030104 developmental biology, 030220 oncology & carcinogenesis, Mutation (genetic algorithm), Spinocerebellar ataxia, Medical genetics, Female, ADCK3

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08c4984e88f0c7f11b7468b4ad77ada8
https://doi.org/10.1016/j.gene.2019.05.016

المؤلفون: A. Kollaee, Habib Nasiri, M J Tahmasebi Birgani, Javad Mohammadi-Asl, K. Riahi, Mohamadreza Hajjari

المصدر: Annals of Human Genetics. 82:304-308

مصطلحات موضوعية: Male, 0301 basic medicine, Microcephaly, Disease, Iran, Biology, Cockayne syndrome, 03 medical and health sciences, Exome Sequencing, Genetics, medicine, Humans, Amino Acid Sequence, Child, Cockayne Syndrome, Gene, Genetics (clinical), Exome sequencing, Sequence Deletion, Genetic heterogeneity, medicine.disease, Pedigree, DNA Repair Enzymes, 030104 developmental biology, ERCC8, Failure to thrive, Female, medicine.symptom, Transcription Factors

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::915c0cd3dc6fb41e31076310d7d4dc12
https://doi.org/10.1111/ahg.12255

المؤلفون: Habib Nasiri, Majid Jafari-Sabet, Ramin Ataee

المصدر: Journal of Archives in Military Medicine. 4

مصطلحات موضوعية: Molar, Chemistry, Cross-link, Extraction (chemistry), 02 engineering and technology, Matrix (biology), 010402 general chemistry, 021001 nanoscience & nanotechnology, 01 natural sciences, 0104 chemical sciences, chemistry.chemical_compound, Tissue engineering, Pharmaceutics, 0210 nano-technology, Wound healing, Nuclear chemistry, Carbodiimide

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::7cb508a78bdfb68811edd2035537be00
https://doi.org/10.5812/jamm.42367

المؤلفون: Mark Meerum Terwogt, Habib Nasiri, Morteza Latifian, Carolien Rieffe, Sheida Novin, Paul Oosterveld

المساهمون: Clinical Developmental Psychology

المصدر: Personality and Individual Differences, 48, 425-430. Elsevier BV
Rieffe, C J, Oosterveld, P, Meerum Terwogt, M, Novin Farahbakhsh, S, Nasiri, H & Latifian, M 2010, ' Relationship between alexithymia, mood and internalizing symptoms in children and young adolescents: Evidence from an Iranian sample ', Personality and Individual Differences, vol. 48, pp. 425-430 . https://doi.org/10.1016/j.paid.2009.11.010

مصطلحات موضوعية: education.field_of_study, media_common.quotation_subject, education, Population, medicine.disease, Developmental psychology, Mood, Alexithymia, Rumination, medicine, Personality, Anxiety, Worry, medicine.symptom, Psychology, General Psychology, Psychopathology, media_common

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1d21e5ff0443a2af60d158bc7a993b0
https://doi.org/10.1016/j.paid.2009.11.010

المؤلفون: Iman Sadeghi, Habib Nasiri, Abbas Salavaty, Maryam Tahmasebi Birgani, Mohammadreza Hajjari

المصدر: Genomics & Informatics
Genomics & Informatics, Vol 14, Iss 4, Pp 234-240 (2016)

مصطلحات موضوعية: 0301 basic medicine, Silent mutation, lcsh:QH426-470, translation, Health Informatics, Biology, 03 medical and health sciences, Genetics, medicine, Gene, Ecology, Evolution, Behavior and Systematics, Regulation of gene expression, chemistry.chemical_classification, apoptosis, Cancer, Translation (biology), gene expression regulation, medicine.disease, Amino acid, lcsh:Genetics, 030104 developmental biology, chemistry, Apoptosis, Codon usage bias, Original Article, codon

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3fd0071f8461402a19da5562d013a26f
https://doi.org/10.5808/gi.2016.14.4.234

المؤلفون: Habib, Nasiri, Mohammad-Reza, Noori-Dalooi, Jila, Dastan, Saeed-Reza, Ghaffari

المصدر: Iranian Journal of Pediatrics

مصطلحات موضوعية: Chromosomal Aberration, Short Tandem Repeats, Prenatal Diagnosis, Original Article, QF-PCR

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::724bd61599dd416dc8f374061f821b7a
https://pubmed.ncbi.nlm.nih.gov/23056758