Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Ziba Morovvati"'
Autor:
Marzieh Rahbaran, Maryam Hassani Doabsari, Simindokht Salavitabar, Neda Mokhberian, Ziba Morovvati, Saeid Morovvati
Publikováno v:
Cellular & Molecular Biology Letters, Vol 24, Iss 1, Pp 1-8 (2019)
Abstract Purpose Ectodermal dysplasias are characterized by developmental abnormalities in ectodermal structures. Hypohidrotic ectodermal dysplasias (HED) are the most common subtype. They are most commonly inherited via X-linked recessive routes. We
Externí odkaz:
https://doaj.org/article/41baa1c3fec74390b0eca820f9c5c84a
Autor:
Ehsan Moghanloo, Ziba Morovvati, Maghsoud Seifi, Fatemeh Minoochehr, Saeid Morovvati, Shahram Teimourian
Publikováno v:
Iranian Journal of Medical Sciences, Vol 44, Iss 3, Pp 262-264 (2019)
Hereditary ataxias (HA) are a group of inherited neurological disorders caused by changes in genes. At least 115 different mutations in the senataxin (SETX) gene causing ataxia have been identified. There are no reports of any SETX gene mutation amon
Externí odkaz:
https://doaj.org/article/65fa829adb124f0fbc6059ad6daabf63
Autor:
Saeid Morovvati, Paniz Farshadyeganeh, Mojdeh Hamidizadeh, Ziba Morovvati, Samaneh Doost Mohammadi
Publikováno v:
Acta Medica Iranica, Vol 56, Iss 7 (2018)
Lipoid proteinosis (LP) is a rare autosomal recessive disorder caused by malfunction mutations in extracellular matrix protein 1 gene (ECM1) with common features such as hoarseness of the voice, infiltration of the skin and mucosa, and varying degree
Externí odkaz:
https://doaj.org/article/337ba50df44f42cc99eae0495b8ec93d
Autor:
Ziba Morovvati, Saeid Morovvati, Gholamhossein Alishiri, Seyed Hossein Moosavi, Reza Ranjbar, Yaser Bolouki Moghaddam
Publikováno v:
Cell Journal, Vol 16, Iss 1, Pp 91-94 (2014)
Fibrodysplasia Ossificans Progressiva (FOP, MIM 135100) is a rare genetic disease that is often inherited sporadically in an autosomal dominant pattern. The disease manifests in early life with malformed great toes and, its episodic and progressive b
Externí odkaz:
https://doaj.org/article/da0d15006da1484aac8e0e042174ce80
Publikováno v:
Cell Journal, Vol 13, Iss 2, Pp 103-106 (2011)
Objective: Mitochondrial DNA (mtDNA) is a useful tool for population studies, identificationof humans and forensic DNA studies. The existence of several hundreds copies ofmtDNA per cell permit its extraction from minute or degraded samples. In additi
Externí odkaz:
https://doaj.org/article/0bc7692a4ffe402298ee4bb39753bb6a
Autor:
Neda Mokhberian, Ziba Morovvati, Simindokht Salavitabar, Marzieh Rahbaran, Maryam Hassani Doabsari, Saeid Morovvati
Publikováno v:
Cellular & Molecular Biology Letters, Vol 24, Iss 1, Pp 1-8 (2019)
Cellular & Molecular Biology Letters
Cellular & Molecular Biology Letters
Purpose Ectodermal dysplasias are characterized by developmental abnormalities in ectodermal structures. Hypohidrotic ectodermal dysplasias (HED) are the most common subtype. They are most commonly inherited via X-linked recessive routes. We report o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23157d9bb2c322881c968071a3be73d8
http://link.springer.com/article/10.1186/s11658-019-0174-9
http://link.springer.com/article/10.1186/s11658-019-0174-9
Publikováno v:
International Journal of Medical Laboratory.
Background and Aims: Azoospermia factor (AZF) region of the Ychromosome has several genes which are responsible for normal spermatogenesis. Microdeletions of these genes are associated with azoospermia and oligospermia. These microdeletions are too s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bc1e8577f9197206c29cd2636621c37f
https://doi.org/10.18502/ijml.v7i2.2918
https://doi.org/10.18502/ijml.v7i2.2918