المؤلفون: Vahid Nasiri, Farnoosh Jameie, Habibollah Paykari, Nahideh Mazhari, Saba Soltani, Mahdieh Pashaei

المصدر: Journal of Veterinary Science and Research, 1(1), 78-91, (2019-12-13)

مصطلحات موضوعية: Wild animals, Zoological park, Parasite, Iran

Relation: https://doi.org/10.36811/jvsr.2019.110009; oai:zenodo.org:3589381

الاتاحة: https://doi.org/10.36811/jvsr.2019.110009

المؤلفون: Reza Hajati, Atefeh Davarzani, Mahdieh Pashaei, Farzaneh Larti, Afagh Alavi, Babak Zamani, Shahriar Nafissi, Mohammad Rohani, Yalda Nilipour

المصدر: Journal of neurogenetics. 35(2)

مصطلحات موضوعية: 0301 basic medicine, Proband, Adult, Male, Adolescent, Hereditary spastic paraplegia, Cytochrome P450 Family 7, Disease, Biology, Genetic analysis, 03 medical and health sciences, Cellular and Molecular Neuroscience, Young Adult, 0302 clinical medicine, Exome Sequencing, Genetics, medicine, Humans, Child, Gene, Genetic heterogeneity, Spastic Paraplegia, Hereditary, Apyrase, medicine.disease, Phenotype, Pedigree, 030104 developmental biology, Child, Preschool, Mutation, Steroid Hydroxylases, Allelic heterogeneity, Female, Carrier Proteins, 030217 neurology & neurosurgery

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c2cd962763332dfd6ca3c6b40906cf4
https://pubmed.ncbi.nlm.nih.gov/33771085

المؤلفون: Mahdieh Pashaei (10485652), Atefeh Davarzani (10485655), Reza Hajati (10485658), Babak Zamani (9302810), Shahriar Nafissi (547379), Farzaneh Larti (10485661), Yalda Nilipour (6041981), Mohammad Rohani (9302807), Afagh Alavi (6041975)

مصطلحات موضوعية: Biochemistry, Medicine, Genetics, Neuroscience, Cancer, Computational Biology, Space Science, Biological Sciences not elsewhere classified, Hereditary spastic paraplegia (HSP), CYP7B1 (SPG5A), ENTPD1 (SPG64), ZFYVE26 (SPG15), Whole-exome sequencing (WES)

Relation: https://figshare.com/articles/dataset/Description_of_clinical_features_and_genetic_analysis_of_one_ultra-rare_SPG64_and_two_common_forms_SPG5A_and_SPG15_of_hereditary_spastic_paraplegia_families/14329075

الاتاحة: https://doi.org/10.6084/m9.figshare.14329075.v1

المؤلفون: Hossein Najmabadi, Farzad Fatehi, Ramona Haji-Seyed-Javadi, Afagh Alavi, Mahdieh Pashaei, Davood Zare-Abdollahi, Mohammad Masoud Rahimi Bidgoli

المصدر: J Assist Reprod Genet

مصطلحات موضوعية: 0301 basic medicine, Infertility, Proband, Adult, Male, endocrine system, Hereditary spastic paraplegia, Biology, urologic and male genital diseases, Male infertility, 03 medical and health sciences, Consanguinity, Mice, 0302 clinical medicine, Exome Sequencing, medicine, Genetics, Animals, Humans, Genetic Predisposition to Disease, Central element, Genetics (clinical), Infertility, Male, Azoospermia, 030219 obstetrics & reproductive medicine, Splice site mutation, Homozygote, Obstetrics and Gynecology, General Medicine, medicine.disease, Pedigree, DNA-Binding Proteins, Synaptonemal complex, Meiosis, 030104 developmental biology, Reproductive Medicine, Codon, Nonsense, Mutation, RNA Splice Sites, Developmental Biology

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::efbff1f63868126c590414b7dd7c2f2d
https://pubmed.ncbi.nlm.nih.gov/31916078