Ghanbari A - Search Results

1

Frequencies of gap- and tight-junction mutations in Turkish families with autosomal-recessive non-syndromic hearing loss.

Uyguner O, Emiroglu M, Uzumcu A, Hafiz G, Ghanbari A, Baserer N, Yuksel-Apak M, Wollnik B. Uyguner O, et al. Among authors: ghanbari a. Clin Genet. 2003 Jul;64(1):65-9. doi: 10.1034/j.1399-0004.2003.00101.x. Clin Genet. 2003. PMID: 12791041

2

Homozygous and heterozygous inheritance of PAX3 mutations causes different types of Waardenburg syndrome.

Wollnik B, Tukel T, Uyguner O, Ghanbari A, Kayserili H, Emiroglu M, Yuksel-Apak M. Wollnik B, et al. Among authors: ghanbari a. Am J Med Genet A. 2003 Sep 15;122A(1):42-5. doi: 10.1002/ajmg.a.20260. Am J Med Genet A. 2003. PMID: 12949970

3

The novel R75Q mutation in the GJB2 gene causes autosomal dominant hearing loss and palmoplantar keratoderma in a Turkish family.

Uyguner O, Tukel T, Baykal C, Eris H, Emiroglu M, Hafiz G, Ghanbari A, Baserer N, Yuksel-Apak M, Wollnik B. Uyguner O, et al. Among authors: ghanbari a. Clin Genet. 2002 Oct;62(4):306-9. doi: 10.1034/j.1399-0004.2002.620409.x. Clin Genet. 2002. PMID: 12372058

4

The identification of small supernumerary marker chromosomes; the experiences of 15,792 fetal karyotyping from Turkey.

Karaman B, Aytan M, Yilmaz K, Toksoy G, Onal EP, Ghanbari A, Engur A, Kayserili H, Yuksel-Apak M, Basaran S. Karaman B, et al. Among authors: ghanbari a. Eur J Med Genet. 2006 May-Jun;49(3):207-14. doi: 10.1016/j.ejmg.2005.06.002. Epub 2005 Jul 12. Eur J Med Genet. 2006. PMID: 16762822

5

The results of cytogenetic analysis with regard to intracytoplasmic sperm injection in males, females and fetuses.

Basaran S, Engur A, Aytan M, Karaman B, Ghanbari A, Toksoy G, Yuksel A, Cankat D, Kervancioglu E, Wollnik B, Bahceci M, Yuksel-Apak M. Basaran S, et al. Among authors: ghanbari a. Fetal Diagn Ther. 2004 Jul-Aug;19(4):313-8. doi: 10.1159/000077958. Fetal Diagn Ther. 2004. PMID: 15192289

6

Pallister-Killian syndrome: clinical, cytogenetic and molecular findings in 15 cases.

Karaman B, Kayserili H, Ghanbari A, Uyguner ZO, Toksoy G, Altunoglu U, Basaran S. Karaman B, et al. Among authors: ghanbari a. Mol Cytogenet. 2018 Aug 17;11:45. doi: 10.1186/s13039-018-0395-z. eCollection 2018. Mol Cytogenet. 2018. PMID: 30140312 Free PMC article.

7

Augmentation of neural stem cell proliferation and enhanced differentiation toward neural and oligodendroglia lineages through sonic hedgehog pathway: Cross-activation of Notch1 and SOX10.

Azizi A, Azarmehr N, Shahraki MH, Arynpour R, Enanat E, Fard PD, Barmak MJ, Ghanbari A. Azizi A, et al. Among authors: ghanbari a. Neurosci Lett. 2025 Jan 3:138098. doi: 10.1016/j.neulet.2024.138098. Online ahead of print. Neurosci Lett. 2025. PMID: 39756602

8

Availability and affordability of selected medicines in the Islamic Republic of Iran.

Ghanbari AR, Moazen M, Azizi A, Abdollahiasll A, Soleymani F. Ghanbari AR, et al. East Mediterr Health J. 2024 Oct 1;30(9):632-640. doi: 10.26719/2024.30.9.632. East Mediterr Health J. 2024. PMID: 39574381 Free article.

9

Worldwide trends in diabetes prevalence and treatment from 1990 to 2022: a pooled analysis of 1108 population-representative studies with 141 million participants.

NCD Risk Factor Collaboration (NCD-RisC). NCD Risk Factor Collaboration (NCD-RisC). Lancet. 2024 Nov 23;404(10467):2077-2093. doi: 10.1016/S0140-6736(24)02317-1. Epub 2024 Nov 13. Lancet. 2024. PMID: 39549716 Free PMC article.

10

D-galactose Induces Senescence in Adult Mouse Neural Stem Cells by Imbalanced Oxidant and Antioxidant Activity and Differential Expression of Specific Hub Genes.

Ghanbari A, Danaie Fard P, Azarmehr N, Mahmoudi R, Roozbehi A, Zibara K, Hosseini E. Ghanbari A, et al. Mol Neurobiol. 2024 Oct 19. doi: 10.1007/s12035-024-04546-1. Online ahead of print. Mol Neurobiol. 2024. PMID: 39425831

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