Galehdari H - Search Results

1

PKHD1L1, A Gene Involved in the Stereocilia Coat, Causes Autosomal Recessive Nonsyndromic Hearing Loss.

Redfield SE, De-la-Torre P, Zamani M, Wang H, Khan H, Morris T, Shariati G, Karimi M, Kenna MA, Seo GH, Xu H, Lu W, Naz S, Galehdari H, Indzhykulian AA, Shearer AE, Vona B. Redfield SE, et al. Among authors: galehdari h. medRxiv [Preprint]. 2023 Dec 19:2023.10.08.23296081. doi: 10.1101/2023.10.08.23296081. medRxiv. 2023. PMID: 37873491 Free PMC article. Updated. Preprint.

2

HBV genotyping in HBsAg-positive blood donors from Southwestern Iran.

Kohshour MO, Galehdari H, Foroughmand AM, Andashti B, Jalalifar MA, Bidmeshkipour A. Kohshour MO, et al. Among authors: galehdari h. Hepat Mon. 2010 Spring;10(2):147-8. Epub 2010 Jun 1. Hepat Mon. 2010. PMID: 22312388 Free PMC article. No abstract available.

3

Homology modeling and molecular dynamics simulation of odonthubuthus doriae (Od1) scorpion toxin in comparison to the BmK M1.

Karimi Z, Falsafi-Zadeh S, Galehdari H, Jalali A. Karimi Z, et al. Among authors: galehdari h. Bioinformation. 2012;8(10):474-8. doi: 10.6026/97320630008474. Epub 2012 May 31. Bioinformation. 2012. PMID: 22715302 Free PMC article.

4

The role of Ca(2+) ions in the complex assembling of protein Z and Z-dependent protease inhibitor: A structure and dynamics investigation.

Karimi Z, Falsafi-Zade S, Galehdari H. Karimi Z, et al. Among authors: galehdari h. Bioinformation. 2012;8(9):407-11. doi: 10.6026/97320630008407. Epub 2012 May 15. Bioinformation. 2012. PMID: 22715309 Free PMC article.

5

Deficiency of terminal ADP-ribose protein glycohydrolase TARG1/C6orf130 in neurodegenerative disease.

Sharifi R, Morra R, Appel CD, Tallis M, Chioza B, Jankevicius G, Simpson MA, Matic I, Ozkan E, Golia B, Schellenberg MJ, Weston R, Williams JG, Rossi MN, Galehdari H, Krahn J, Wan A, Trembath RC, Crosby AH, Ahel D, Hay R, Ladurner AG, Timinszky G, Williams RS, Ahel I. Sharifi R, et al. Among authors: galehdari h. EMBO J. 2013 May 2;32(9):1225-37. doi: 10.1038/emboj.2013.51. Epub 2013 Mar 12. EMBO J. 2013. PMID: 23481255 Free PMC article.

6

Frequent loss of heterozygosity at 8p22 chromosomal region in diffuse type of gastric cancer.

Hosseini HA, Ahani A, Galehdari H, Froughmand AM, Hosseini M, Masjedizadeh A, Zali MR. Hosseini HA, et al. Among authors: galehdari h. World J Gastroenterol. 2007 Jun 28;13(24):3354-8. doi: 10.3748/wjg.v13.i24.3354. World J Gastroenterol. 2007. PMID: 17659675 Free PMC article.

7

CYP2E1*5B, CYP2E1*6, CYP2E1*7B, CYP2E1*2, and CYP2E1*3 allele frequencies in iranian populations.

Shahriary GM, Galehdari H, Jalali A, Zanganeh F, Alavi SM, Aghanoori MR. Shahriary GM, et al. Among authors: galehdari h. Asian Pac J Cancer Prev. 2012;13(12):6505-10. doi: 10.7314/apjcp.2012.13.12.6505. Asian Pac J Cancer Prev. 2012. PMID: 23464483 Free article.

8

VMD DisRg: New User-Friendly Implement for calculation distance and radius of gyration in VMD program.

Falsafi-Zadeh S, Karimi Z, Galehdari H. Falsafi-Zadeh S, et al. Among authors: galehdari h. Bioinformation. 2012;8(7):341-3. doi: 10.6026/97320630008341. Epub 2012 Apr 13. Bioinformation. 2012. PMID: 22553393 Free PMC article.

9

Identification of IVS-I (-1) (G > C) or Hb Monroe as a report on the beta-globin gene with a beta-thalassemia minor phenotype in south of Iran.

Hamid M, Shariati G, Saberi A, Kaikhaei B, Galehdari H, Mohammadi-Anaei M. Hamid M, et al. Among authors: galehdari h. Arch Iran Med. 2013 Sep;16(9):563-4. Arch Iran Med. 2013. PMID: 23981164

10

Exon sequencing of PKD1 gene in an Iranian patient with autosomal-dominant polycystic kidney disease.

Hafizi A, Khatami SR, Galehdari H, Shariati G, Saberi AH, Hamid M. Hafizi A, et al. Among authors: galehdari h. Iran Biomed J. 2014 Jul;18(3):143-50. doi: 10.6091/ibj.1317.2014. Iran Biomed J. 2014. PMID: 24842140 Free PMC article.

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