Mocan G - Search Results

1

Characterization of a Novel Frameshift Mutation Within the TRPS1 Gene Causing Trichorhinophalangeal Syndrome Type 1 in a Kindred Cypriot Family.

Ergoren MC, Akcan N, Manara E, Paolacci S, Fahrioğlu U, Betmezoglu M, Bundak R, Mocan G, Temel SG, Bertelli M. Ergoren MC, et al. Among authors: mocan g. Appl Immunohistochem Mol Morphol. 2022 Oct 1;30(9):635-639. doi: 10.1097/PAI.0000000000001056. Epub 2022 Sep 13. Appl Immunohistochem Mol Morphol. 2022. PMID: 36093893

2

Identification of a Novel De Novo COMP Gene Variant as a Likely Cause of Pseudoachondroplasia.

Tuncel G, Akcan N, Gul S, Sag SO, Bundak R, Mocan G, Temel SG, Ergoren MC. Tuncel G, et al. Among authors: mocan g. Appl Immunohistochem Mol Morphol. 2021 Aug 1;29(7):546-550. doi: 10.1097/PAI.0000000000000914. Appl Immunohistochem Mol Morphol. 2021. PMID: 33595934

3

Identification and characterization of a novel FBN1 gene variant in an extended family with variable clinical phenotype of Marfan syndrome.

Ergoren MC, Turkgenc B, Teralı K, Rodoplu O, Verstraeten A, Van Laer L, Mocan G, Loeys B, Tetik O, Temel SG. Ergoren MC, et al. Among authors: mocan g. Connect Tissue Res. 2019 Mar;60(2):146-154. doi: 10.1080/03008207.2018.1472589. Epub 2018 May 28. Connect Tissue Res. 2019. PMID: 29732924

4

CCR5-Δ32 gene variant frequency in the Turkish Cypriot population.

Fahrioglu U, Ergoren MC, Mocan G. Fahrioglu U, et al. Among authors: mocan g. Braz J Microbiol. 2020 Dec;51(4):1711-1717. doi: 10.1007/s42770-020-00352-8. Epub 2020 Jul 31. Braz J Microbiol. 2020. PMID: 32734471 Free PMC article.

5

The Story of a Ship Journey, Malaria, and the HBB Gene IVS-II-745 Mutation: Circassian Immigration to Cyprus.

Ergoren MC, Temel SG, Mocan G, Dundar M. Ergoren MC, et al. Among authors: mocan g. Glob Med Genet. 2021 Jun;8(2):69-71. doi: 10.1055/s-0041-1726336. Epub 2021 Mar 16. Glob Med Genet. 2021. PMID: 33987626 Free PMC article.

6

Natural selection at work? Vitamin D deficiency rates and rising health problems in young Turkish Cypriot professionals.

Kandemiş E, Tuncel G, Fahrioğlu U, Temel ŞG, Mocan G, Ergören MÇ. Kandemiş E, et al. Among authors: mocan g. Cent Eur J Public Health. 2021 Jun;29(2):130-133. doi: 10.21101/cejph.a6117. Cent Eur J Public Health. 2021. PMID: 34245553 Free article.

7

Psychomotor Delay in a Child with FGFR3 G380R Pathogenic Mutation Causing Achondroplasia.

Ergoren MC, Eren E, Manara E, Paolacci S, Tulay P, Sag SO, Bertelli M, Mocan G, Temel SG. Ergoren MC, et al. Among authors: mocan g. Glob Med Genet. 2021 Sep;8(3):100-103. doi: 10.1055/s-0041-1725070. Epub 2021 May 21. Glob Med Genet. 2021. PMID: 34430961 Free PMC article.

8

Functional coding/non-coding variants in EGFR, ROS1 and ALK genes and their role in liquid biopsy as a personalized therapy.

Ergoren MC, Cobanogulları H, Temel SG, Mocan G. Ergoren MC, et al. Among authors: mocan g. Crit Rev Oncol Hematol. 2020 Dec;156:103113. doi: 10.1016/j.critrevonc.2020.103113. Epub 2020 Sep 28. Crit Rev Oncol Hematol. 2020. PMID: 33038629 Review.

9

The expression profile of WNT/β-catanin signalling genes in human oocytes obtained from polycystic ovarian syndrome (PCOS) patients.

Ismail AB, Naji M'S, Nebih İ, Tuncel G, Ozbakir B, Temel SG, Tulay P, Mocan G, Ergoren MC. Ismail AB, et al. Among authors: mocan g. Zygote. 2022 Aug;30(4):536-542. doi: 10.1017/S0967199422000028. Epub 2022 Mar 31. Zygote. 2022. PMID: 35357301

10

CCR5-Δ32 gene variant frequency in the Nigerian and Zimbabwean populations living in North Cyprus.

Ndikom BC, Ergoren MC, Sayan M, Mocan G, Fahrioğlu U. Ndikom BC, et al. Among authors: mocan g. Afr Health Sci. 2022 Mar;22(1):361-366. doi: 10.4314/ahs.v22i1.44. Afr Health Sci. 2022. PMID: 36032469 Free PMC article.

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