Zobrazeno 1 - 10
of 16
pro vyhledávání: '"A Tolooi"'
Autor:
M Hashemzadeh Chaleshtori, L Hoghooghi Rad, M Dolati, R Sasanfar, A Hoseinipour, M Montazer Zohour, H Pourjafari, A Tolooi, M Ghadami, DD Farhud, MA Patton
Publikováno v:
Iranian Journal of Public Health, Vol 34, Iss 1, Pp 1-7 (2005)
While hearing loss has been considered to be a very heterogeneous disorder, mutations in Gap junction beta 2 (GJB2) gene encoding Connexin 26 (Cx26) protein are the major cause of autosomal recessive and sporadic non-syndromic deafness in many popula
Externí odkaz:
https://doaj.org/article/5e3612f03f464d559a75c18adfbc9247
Autor:
A Hosseinipour, M Hashemzadeh Chaleshtori, R Sasanfar, DD Farhud, A Tolooi, M Doulati, L Hoghooghi Rad, M Montazer zohour, M Ghadami
Publikováno v:
Iranian Journal of Public Health, Vol 34, Iss 1, Pp 47-50 (2005)
Autosomal recessive and sporadic non-syndromic hearing loss (ARSNSHL) is the major form of hereditary deafness.Mutations in the GJB2 gene encoding the gap-junction protein Connexin 26 have been identified to be highly associated with ARSNSHL. In this
Externí odkaz:
https://doaj.org/article/b7821cb7395c4601940b4fc2ffa18cf5
Autor:
M Hashemzadeh Chaleshtori, M Dowlati, DD Farhud, L Hoghooghi Rad, R Sasanfar A Hoseinipour, M Montazer Zohour, A Tolooi, M Ghadami, HR Pourjafari, MA Oshaghi, MA Patton "
Publikováno v:
Iranian Journal of Public Health, Vol 33, Iss 2, Pp 14-19 (2004)
Mutations in the GJB2 gene encoding Connexin 26 (Cx26) protein are a major cause for autosomal recessive non syndromic and sporadic deafness in many populations. In this study we have investigated the prevalence of the GJB2 gene mutations using neste
Externí odkaz:
https://doaj.org/article/a458d4a14e3543a18e8b538ea71f31ec
Publikováno v:
Revista Fatec Zona Sul, Vol 4, Iss 4, Pp 1-13 (2018)
Dentro da matriz de transporte brasileira o transporte rodoviário responde por 65% do total de mercadorias transportadas sendo que em relação ao PIB, o transporte equivale a 6,8% dos custos logísticos. Este artigo tem como objetivo apresentar as
Externí odkaz:
https://doaj.org/article/db3ad3c778ee40c5856ab397a81294d6
Autor:
Niloofar Tolooi
Publikováno v:
Jentashapir Journal of Cellular and Molecular Biology. 12
Background: The paraoxonase1 gene (PON1) is part of the paraoxonase family of multifactorial antioxidants (EC 3.1.1.2). The functional single-nucleotide polymorphisms L55M and Q192R are located in the coding site of this gene. The association between
Autor:
Niloofar Tolooi, Ahmad Hamta
Publikováno v:
Jentashapir Journal of Cellular and Molecular Biology. 12
Background: Colorectal cancer (CRC) is one of the most common malignant tumors in the world, which has been introduced as the third most common cancer and the third leading cause of death. This cancer is uncommon before the age of 50. Its prognosis i
Autor:
Hosseinipour, A., Chaleshtori, M. H., Sasanfar, R., Farhud, D. D., Tolooi, A., Doulati, M., Rad, L. H., Mostafa Montazer zohour, Ghadami, M.
Publikováno v:
Iranian Journal of Public Health, Vol 34, Iss 1, Pp 47-50 (2005)
Scopus-Elsevier
Iranian Journal of Public Health, Vol 34, Iss 1 (2005)
Scopus-Elsevier
Iranian Journal of Public Health, Vol 34, Iss 1 (2005)
Autosomal recessive and sporadic non-syndromic hearing loss (ARSNSHL) is the major form of hereditary deafness.Mutations in the GJB2 gene encoding the gap-junction protein Connexin 26 have been identified to be highly associated with ARSNSHL. In this
Autor:
'M Hashemzadeh Chaleshtori, M Dowlati, DD Farhud, L Hoghooghi Rad, R Sasanfar A Hoseinipour, M Montazer Zohour, A Tolooi, M Ghadami, HR Pourjafari, MA Oshaghi, MA Patton \\'
Publikováno v:
Iranian Journal of Public Health, Vol 33, Iss 2 (2004)
Iranian Journal of Public Health, Vol 33, Iss 2, Pp 14-19 (2004)
Iranian Journal of Public Health, Vol 33, Iss 2, Pp 14-19 (2004)
Mutations in the GJB2 gene encoding Connexin 26 (Cx26) protein are a major cause for autosomal recessive non syndromic and sporadic deafness in many populations. In this study we have investigated the prevalence of the GJB2 gene mutations using neste
Autor:
morteza hashemzadeh Chaleshtori, Hoghooghi Rad, L., Dolati, M., Sasanfar, R., Hoseinipour, A., Montazer Zohour, M., Pourjafari, H., Tolooi, A., Ghadami, M., Farhud, D. D., Patton, M. A.
Publikováno v:
Scopus-Elsevier
Iranian Journal of Public Health, Vol 34, Iss 1, Pp 1-7 (2005)
Iranian Journal of Public Health, Vol 34, Iss 1 (2005)
Iranian Journal of Public Health, Vol 34, Iss 1, Pp 1-7 (2005)
Iranian Journal of Public Health, Vol 34, Iss 1 (2005)
While hearing loss has been considered to be a very heterogeneous disorder, mutations in Gap junction beta 2 (GJB2) gene encoding Connexin 26 (Cx26) protein are the major cause of autosomal recessive and sporadic non-syndromic deafness in many popula
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::4f456fe9adfbf64858e4bc628ce9b61c
http://www.scopus.com/inward/record.url?eid=2-s2.0-25444504571&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-25444504571&partnerID=MN8TOARS
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