Dogan ME - Search Results

1

EVs vs. EVs: MSCs and Tregs as a source of invisible possibilities.

Heydari Z, Peshkova M, Gonen ZB, Coretchi I, Eken A, Yay AH, Dogan ME, Gokce N, Akalin H, Kosheleva N, Galea-Abdusa D, Ulinici M, Vorojbit V, Shpichka A, Groppa S, Vosough M, Todiras M, Butnaru D, Ozkul Y, Timashev P. Heydari Z, et al. Among authors: dogan me. J Mol Med (Berl). 2023 Feb;101(1-2):51-63. doi: 10.1007/s00109-022-02276-2. Epub 2022 Dec 17. J Mol Med (Berl). 2023. PMID: 36527475 Free PMC article. Review.

2

The molecular basis and genotype-phenotype correlations of congenital adrenal hyperplasia (CAH) in Anatolian population.

Dundar A, Bayramov R, Onal MG, Akkus M, Dogan ME, Kenanoglu S, Cerrah Gunes M, Kazimli U, Ozbek MN, Ercan O, Yildirim R, Celmeli G, Parlak M, Dundar I, Hatipoglu N, Unluhizarci K, Akalin H, Ozkul Y, Saatci C, Dundar M. Dundar A, et al. Among authors: dogan me. Mol Biol Rep. 2019 Aug;46(4):3677-3690. doi: 10.1007/s11033-019-04809-4. Epub 2019 Apr 20. Mol Biol Rep. 2019. PMID: 31006099

3

A rare cause of membranoproliferative patterns of injury in siblings with steroid-resistant nephrotic syndrome: Questions.

Günay N, Pınarbaşı AS, Doğan ME, Yel S, Balaban AG, Dursun İ, Eken A, Akgün H, Dündar M, Poyrazoğlu MH. Günay N, et al. Among authors: dogan me. Pediatr Nephrol. 2021 Dec;36(12):4027-4028. doi: 10.1007/s00467-021-05138-0. Epub 2021 Jun 29. Pediatr Nephrol. 2021. PMID: 34185134 No abstract available.

4

A rare cause of membranoproliferative patterns of injury in siblings with steroid-resistant nephrotic syndrome: Answers.

Günay N, Pınarbaşı AS, Doğan ME, Yel S, Balaban AG, Dursun İ, Eken A, Akgün H, Dündar M, Poyrazoğlu MH. Günay N, et al. Among authors: dogan me. Pediatr Nephrol. 2021 Dec;36(12):4029-4032. doi: 10.1007/s00467-021-05154-0. Epub 2021 Jun 29. Pediatr Nephrol. 2021. PMID: 34185135 No abstract available.

5

The Effect of Gene Mutations on Metastasis and Overall Survival in Metastatic and Nonmetastatic Colon Cancers.

Ozdemir Y, Cag M, Colak E, Coskun N, Basgoz N, Sarici H, Kaan D, Dogan M, Deniz K, Inanc M, Ozkul Y. Ozdemir Y, et al. Asian Pac J Cancer Prev. 2021 Dec 1;22(12):3839-3846. doi: 10.31557/APJCP.2021.22.12.3839. Asian Pac J Cancer Prev. 2021. PMID: 34967562 Free PMC article.

6

A novel missense mutation outside the DNAJ domain of DNAJC21 is associated with Shwachman-Diamond syndrome.

Alsavaf MB, Verboon JM, Dogan ME, Azizoglu ZB, Okus FZ, Ozcan A, Dundar M, Eken A, Donmez-Altuntas H, Sankaran VG, Unal E. Alsavaf MB, et al. Among authors: dogan me. Br J Haematol. 2022 Jun;197(6):e88-e93. doi: 10.1111/bjh.18112. Epub 2022 Mar 17. Br J Haematol. 2022. PMID: 35298850 No abstract available.

7

Change in gene expression levels of GABA, glutamate and neurosteroid pathways due to acoustic trauma in the cochlea.

Cerrah Gunes M, Gunes MS, Vural A, Aybuga F, Bayram A, Bayram KK, Sahin MI, Dogan ME, Ozdemir SY, Ozkul Y. Cerrah Gunes M, et al. Among authors: dogan me. J Neurogenet. 2021 Mar;35(1):45-57. doi: 10.1080/01677063.2021.1904922. Epub 2021 Apr 7. J Neurogenet. 2021. PMID: 33825593

8

Pyruvate kinase deficiency in 29 Turkish patients with two novel intronic variants.

Gök V, Leblebisatan G, Gürlek Gökçebay D, Güler S, Doğan ME, Tuğ Bozdoğan S, Koca Yozgat A, Özcan A, Pekpak Şahinoğlu E, Tokgöz H, Çil M, Özemri Sağ Ş, Yilmaz E, Şaşmaz Hİ, Evim MS, Akbayram S, Karadoğan M, Mutlu FT, Boğa İ, Yeter Doğan B, Yarali N, Çalişkan Ü, Bişgin A, Temel ŞG, Proven M, Gibson K, Demir BŞ, Saraçoğlu H, Eken A, Karakükçü Ç, Karakükçü M, Güneş AM, Özbek NY, Kilinç Y, Patiroğlu T, Özdemir MA, Roy NBA, Ünal E. Gök V, et al. Among authors: dogan me. Br J Haematol. 2024 Jul;205(1):236-242. doi: 10.1111/bjh.19575. Epub 2024 May 29. Br J Haematol. 2024. PMID: 38811201

9

Increased vitamin D receptor gene expression and rs11568820 and rs4516035 promoter polymorphisms in autistic disorder.

Balta B, Gumus H, Bayramov R, Korkmaz Bayramov K, Erdogan M, Oztop DB, Dogan ME, Taheri S, Dundar M. Balta B, et al. Among authors: dogan me. Mol Biol Rep. 2018 Aug;45(4):541-546. doi: 10.1007/s11033-018-4191-y. Epub 2018 May 18. Mol Biol Rep. 2018. PMID: 29777458

10

A novel MTX2 gene splice site variant resulting in exon skipping, causing the recently described mandibuloacral dysplasia progeroid syndrome.

Yeter Doğan B, Günay N, Ada Y, Doğan ME. Yeter Doğan B, et al. Among authors: dogan me. Am J Med Genet A. 2023 Jan;191(1):173-182. doi: 10.1002/ajmg.a.63010. Epub 2022 Oct 21. Am J Med Genet A. 2023. PMID: 36269149

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