Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Fereshteh Chitsazian"'
Autor:
Fereshteh Esfandiari, Fereshteh Chitsazian, Masoumeh Golestan Jahromi, Raha Favaedi, Masood Bazrgar, Reza Aflatoonian, Parvaneh Afsharian, Abbas Aflatoonian, Maryam Shahhoseini
Publikováno v:
Reproductive Biology and Endocrinology, Vol 19, Iss 1, Pp 1-10 (2021)
Abstract Endometriosis is major gynecological disease that affects over 10% of women worldwide and 30%-50% of these women have pelvic pain, abnormal uterine bleeding and infertility. The cause of endometriosis is unknown and there is no definite cure
Externí odkaz:
https://doaj.org/article/60c567744ed04721916bad1c427b9429
Autor:
Marzieh Khani, Shahriar Nafissi, Hosein Shamshiri, Hamidreza Moazzeni, Hanieh Taheri, Mehdi Sadeghi, Najmeh Salehi, Fereshteh Chitsazian, Elahe Elahi
Publikováno v:
European journal of neurologyREFERENCES. 29(12)
Spinal-bulbar muscular atrophy (SBMA) (Kennedy's disease) is a motor neuron disease. Kennedy's disease is nearly exclusively caused by mutations in the androgen receptor encoding gene (AR). The results of studies aimed at identification of the geneti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::245c71f9292f336daa8b357def7b9fd4
https://pubmed.ncbi.nlm.nih.gov/35996994
https://pubmed.ncbi.nlm.nih.gov/35996994
Autor:
Fatemeh Suri, Fereshteh Chitsazian, Betsabeh Khoramian-Tusi, Heidar Amini, Shahin Yazdani, Naveed Nilforooshan, S. Jalal Zargar, Elahe Elahi
Publikováno v:
Journal of Ophthalmic & Vision Research, Vol 4, Iss 2, Pp 75-78 (2009)
PURPOSE: To investigate variations in sex ratio among Iranian primary congenital glaucoma (PCG) patients with and without mutations in the CYP1B1 gene and to evaluate possible clinical variations associated with sex in these two groups. METHODS: Phen
Externí odkaz:
https://doaj.org/article/af604efc3c9f427db52b5496586d7b92
Autor:
Masoumeh Golestan Jahromi, Masood Bazrgar, Fereshteh Esfandiari, Fereshteh Chitsazian, Reza Aflatoonian, Maryam Shahhoseini, Parvaneh Afsharian, Abbas Aflatoonian, Raha Favaedi
Publikováno v:
Reproductive Biology and Endocrinology : RB&E
Reproductive Biology and Endocrinology, Vol 19, Iss 1, Pp 1-10 (2021)
Reproductive Biology and Endocrinology, Vol 19, Iss 1, Pp 1-10 (2021)
Endometriosis is major gynecological disease that affects over 10% of women worldwide and 30%-50% of these women have pelvic pain, abnormal uterine bleeding and infertility. The cause of endometriosis is unknown and there is no definite cure mainly b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a63149c43b9879a943ac0bdde794854
http://europepmc.org/articles/PMC8409001
http://europepmc.org/articles/PMC8409001
Autor:
Fereshteh Esfandiari, Simin Yari, Hossein Baharvand, Raha Favaedi, Fereshteh Chitsazian, Maryam Shahhoseini, Heidar Heidari-Khoei, Abbas Piryaei, Firouzeh Ghafari
Publikováno v:
Fertility and sterility. 115(1)
Objective To evaluate and compare the methylation pattern of Human Homeobox (HOX) clusters (A–D) and HOX cofactors in normal, eutopic, and ectopic endometrial tissues with ectopic and eutopic endometriosis organoids as advanced preclinical research
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3e7df5a7cacfb8260a48fe59556ddb5
https://pubmed.ncbi.nlm.nih.gov/33413960
https://pubmed.ncbi.nlm.nih.gov/33413960
Autor:
Maryam Shahhoseini, Masood Bazrgar, Parvaneh Afsharian, Fereshteh Chitsazian, Masoumeh Golestan Jahromi, Reza Aflatoonian, Raha Favaedi, Abbas Aflatoonian
Background: Dysregulation of some HOX genes are important for the development of endometriosis. Endometriosis is a complex gynecologic disorder affecting as many as 10-15% of premenopausal women. The pathogenesis of endometriosis, as the presence of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6bc65617ee0db02742c85aae3f5e9b0
https://doi.org/10.21203/rs.2.19857/v1
https://doi.org/10.21203/rs.2.19857/v1
Autor:
Tahereh Poursaberi, Fereshteh Chitsazian, S. Mojtaba Mostafavi, Ali Akbar Miran Beigi, Mohammad Teymouri, Shahram Abolhassan Tash, Parviz Soleimani, Mojtaba Shamsipur
Publikováno v:
Biodegradation. 23:311-318
Methyl tert-butyl ether (MTBE) is widely used as gasoline oxygenate and octane number enhancer for more complete combustion in order to reduce the air pollution caused by motor vehicle exhaust. The possible adverse effects of MTBE on human health are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd483923c01177d7d8e3c3a69e95c44d
https://doi.org/10.1007/s10532-011-9510-0
https://doi.org/10.1007/s10532-011-9510-0
Autor:
Brandy Klotzle, Elham Jaberi, Masoud Houshmand, Elahe Elahi, Mohammad Rohani, Iman Safari, Maryam Malakouti Nejad, Farzad Sina, Fereshteh Chitsazian, Gholam Ali Shahidi
Publikováno v:
Journal of human genetics. 58(8)
SUCLA2 is one of several nuclear-encoded genes that can cause encephalomyopathy accompanied by mitochondrial DNA depletion. The disorder usually manifests in early childhood and leads to early death. The gene encodes one of the subunits of succinyl-C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a7a0386080bde260e9fd686edac5dd1
https://pubmed.ncbi.nlm.nih.gov/23759946
https://pubmed.ncbi.nlm.nih.gov/23759946
Autor:
Behnaz, Bayat, Shahin, Yazdani, Afagh, Alavi, Mohsen, Chiani, Fereshteh, Chitsazian, Betsabeh Khoramian, Tusi, Fatemeh, Suri, Mehrnaz, Narooie-Nejhad, Mohammad H, Sanati, Elahe, Elahi
Publikováno v:
Molecular Vision
Purpose To investigate the role of MYOC and CYP1B1 in Iranian juvenile open angle glaucoma (JOAG) patients. Methods Twenty-three JOAG probands, their available affected and unaffected family members, and 100 ethnically matched control individuals wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d6b6986e0e14782e71cb3f8166d7d82f
https://pubmed.ncbi.nlm.nih.gov/18385784
https://pubmed.ncbi.nlm.nih.gov/18385784
Autor:
Mehdi Sadeghi, Yadollah Eslami, Shahin Yazdani, Reza Zareei, Akram Rismanchian, Elahe Elahi, Navid Nilforooshan, Mohammad Ali Zare Mehrjerdi, Behnaz Bayat, Mohammad Hossein Sanati, Mohammad Pakravan, Ali R. Lasheyee, Mahmood Jabbarvand, Yvonne R. Thorstenson, Mansoor Sarfarazi, Fereshteh Chitsazian, Heidar Amini Saroei, Behnam Ghafarzadeh, Mohammad Rohani, Ali Abdolahi, Betsabeh Khoramian Tusi, Arash Etemadi, Mohammad Mehdi Banoei
Publikováno v:
The Journal of molecular diagnostics : JMD. 9(3)
The mutation spectrum of CYP1B1 among 104 primary congenital glaucoma patients of the genetically heterogeneous Iranian population was investigated by sequencing. We also determined intragenic single nucleotide polymorphism (SNP) haplotypes associate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ac1bfbe4ffb7e1be588de44097de06b
https://pubmed.ncbi.nlm.nih.gov/17591938
https://pubmed.ncbi.nlm.nih.gov/17591938