Moazzeni H - Search Results

1

Diagnosis of cystathionine beta-synthase deficiency by genetic analysis.

Suri F, Narooie-Nejad M, Safari I, Moazzeni H, Rohani MR, Khajeh A, Klotzle B, Fan JB, Elahi E. Suri F, et al. Among authors: moazzeni h. J Neurol Sci. 2014 Dec 15;347(1-2):305-9. doi: 10.1016/j.jns.2014.10.031. Epub 2014 Oct 22. J Neurol Sci. 2014. PMID: 25455305

2

FOXC1 in human trabecular meshwork cells is involved in regulatory pathway that includes miR-204, MEIS2, and ITGβ1.

Paylakhi SH, Moazzeni H, Yazdani S, Rassouli P, Arefian E, Jaberi E, Arash EH, Gilani AS, Fan JB, April C, Amin S, Suri F, Elahi E. Paylakhi SH, et al. Among authors: moazzeni h. Exp Eye Res. 2013 Jun;111:112-21. doi: 10.1016/j.exer.2013.03.009. Epub 2013 Mar 27. Exp Eye Res. 2013. PMID: 23541832

3

Insights into the regulatory molecules involved in glaucoma pathogenesis.

Moazzeni H, Khani M, Elahi E. Moazzeni H, et al. Am J Med Genet C Semin Med Genet. 2020 Sep;184(3):782-827. doi: 10.1002/ajmg.c.31833. Epub 2020 Sep 16. Am J Med Genet C Semin Med Genet. 2020. PMID: 32935930 Review.

4

Non-housekeeping genes expressed in human trabecular meshwork cell cultures.

Paylakhi SH, Yazdani S, April C, Fan JB, Moazzeni H, Ronaghi M, Elahi E. Paylakhi SH, et al. Among authors: moazzeni h. Mol Vis. 2012;18:241-54. Epub 2012 Jan 28. Mol Vis. 2012. PMID: 22312193 Free PMC article.

5

Expression of CXCL6 and BBS5 that may be glaucoma relevant genes is regulated by PITX2.

Moazzeni H, Akbari MT, Yazdani S, Elahi E. Moazzeni H, et al. Gene. 2016 Nov 15;593(1):76-83. doi: 10.1016/j.gene.2016.08.019. Epub 2016 Aug 9. Gene. 2016. PMID: 27520585

6

Identification of RNF13 as cause of recessively inherited ALS in a multi-case pedigree.

Khani M, Nafissi S, Shamshiri H, Moazzeni H, Taheri H, Elahi E. Khani M, et al. Among authors: moazzeni h. J Med Genet. 2022 Jul 25:jmedgenet-2022-108645. doi: 10.1136/jmg-2022-108645. Online ahead of print. J Med Genet. 2022. PMID: 35879052

7

Observation of nine previously reported and 10 non-reported SLC4A11 mutations among 20 Iranian CHED probands and identification of an MPDZ mutation as possible cause of CHED and FECD in one family.

Moazzeni H, Javadi MA, Asgari D, Khani M, Emami M, Moghadam A, Panahi-Bazaz MR, Hosseini Tehrani M, Karimian F, Hosseini B, Nekuie Moghadam T, Hassanpour H, Akbari MT, Elahi E. Moazzeni H, et al. Br J Ophthalmol. 2020 Nov;104(11):1621-1628. doi: 10.1136/bjophthalmol-2019-314377. Epub 2019 Aug 16. Br J Ophthalmol. 2020. PMID: 31420327

8

MicroRNAs that target RGS5.

Banaei-Esfahani A, Moazzeni H, Nosar PN, Amin S, Arefian E, Soleimani M, Yazdani S, Elahi E. Banaei-Esfahani A, et al. Among authors: moazzeni h. Iran J Basic Med Sci. 2015 Feb;18(2):108-14. Iran J Basic Med Sci. 2015. PMID: 25810883 Free PMC article.

9

FMNL2 with Functions Related to the Cytoskeleton is Partially Regulated by PAX6.

Ghorbanpour E, Pasalar P, Yazdani S, Moazzeni H, Elahi E. Ghorbanpour E, et al. Among authors: moazzeni h. J Ophthalmic Vis Res. 2017 Oct-Dec;12(4):407-412. doi: 10.4103/jovr.jovr_8_17. J Ophthalmic Vis Res. 2017. PMID: 29090051 Free PMC article.

10

Identification of genes involved in glaucoma pathogenesis using combined network analysis and empirical studies.

Moazzeni H, Mirrahimi M, Moghadam A, Banaei-Esfahani A, Yazdani S, Elahi E. Moazzeni H, et al. Hum Mol Genet. 2019 Nov 1;28(21):3637-3663. doi: 10.1093/hmg/ddz222. Hum Mol Genet. 2019. PMID: 31518395

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

23 results

Search Page

Filters