RASSOULZADEGAN GRUP

Yayınlar:

1. Yilmaz Sukranli Z, Korkmaz Bayram K, Mehmetbeyoglu E, Doganyigit Z, Beyaz F, Sener EF, Taheri S, Ozkul Y, Rassoulzadegan M. Trans Species RNA Activity: Sperm RNA of the Father of an Autistic Child Programs Glial Cells and Behavioral Disorders in Mice. Biomolecules. 2024 Feb 7;14(2):201. doi: 10.3390/biom14020201.
2. Mehmetbeyoglu E, Duman A, Taheri S, Ozkul Y, Rassoulzadegan M. From Data to Insights: Machine Learning Empowers Prognostic Biomarker Prediction in Autism. J Pers Med. 2023 Dec 15;13(12):1713. doi: 10.3390/jpm13121713.
3. Tufan E, Taheri S, Karaca Z, Mehmetbeyoglu E, Yilmaz Sukranli Z, Korkmaz Bayram K, Ulutabanca H, Tanrıverdi F, Unluhizarci K, Rassoulzadegan M, Kelestimur F. Alterations in serum miR-126-3p levels over time, a marker of pituitary insufficiency following head trauma. Neuroendocrinology. 2023 Dec 9. doi: 10.1159/000535748.
4. Sener EF, Dana H, Tahtasakal R, Hamurcu Z, Taheri S, Delibasi N, Mehmetbeyoglu E, Sukranli ZY, Dal F, Tufan E, Oflamaz AO, Doganyigit Z, Ozkul Y, Rassoulzadegan M. Heterozygous Cc2d1a mice show sex-dependent changes in the Beclin-1/p62 ratio with impaired prefrontal cortex and hippocampal autophagy. Prog Neuropsychopharmacol Biol Psychiatry. 2023 Jul 13;125:110764. doi: 10.1016/j.pnpbp.2023.110764.
5. Taheri S, Karaca Z, Mehmetbeyoglu E, Hamurcu Z, Yilmaz Z, Dal F, Çınar V, Ulutabanca H, Tanriverdi F, Unluhizarci K, Rassoulzadegan M, Kelestimur F. The Role of Apoptosis and Autophagy in the Hypothalamic-Pituitary-Adrenal (HPA) Axis after Traumatic Brain Injury (TBI). Int J Mol Sci. 2022 Dec 10;23(24):15699. doi: 10.3390/ijms232415699.
6. Sener EF, Dana H, Tahtasakal R, Hamurcu Z, Guler A, Tufan E, Doganyigit Z, Rassoulzadegan M. Partial changes in apoptotic pathways in hippocampus and hypothalamus of Cc2d1a heterozygous. Metab Brain Dis. 2023 Feb;38(2):531-541. doi: 10.1007/s11011-022-01125-y.
7. Kocyigit I, Taheri S, Uysal C, Memis M, Ozayturk SG, Zararsiz G, Rassoulzadegan M. Predicting Progression of Autosomal Dominant Polycystic Kidney Disease by Changes in the Telomeric Epigenome. Cells. 2022 Oct 20;11(20):3300. doi: 10.3390/cells11203300.
8. Satir-Basaran G, Kianmehr L, Mehmetbeyoglu E, Korkmaz Bayram K, Memis M, Yilmaz Z, Tufan E, Taheri S, Kelestimur F, Rassoulzadegan M. Mouse Paternal RNAs Initiate a Pattern of Metabolic Disorders in a Line-Dependent Manner. Front Genet. 2022 Mar 28;13:839841. doi: 10.3389/fgene.2022.839841.
9. Mehmetbeyoglu E, Kianmehr L, Borlu M, Yilmaz Z, Basar Kılıc S, Rajabi-Maham H, Taheri S, Rassoulzadegan M. Decrease in RNase HII and Accumulation of lncRNAs/DNA Hybrids: A Causal Implication in Psoriasis? Biomolecules. 2022 Feb 25;12(3):368. doi: 10.3390/biom12030368.
10. Rassoulzadegan M, Sharifi-Zarchi A, Kianmehr L. DNA-RNA Hybrid (R-Loop): From a Unified Picture of the Mammalian Telomere to the Genome-Wide Profile. Cells. 2021 Jun 19;10(6):1556. doi: 10.3390/cells10061556.
11. Wagner N, Ninkov M, Vukolic A, Cubukcuoglu Deniz G, Rassoulzadegan M, Michiels JF, Wagner KD. Implications of the Wilms’ Tumor Suppressor Wt1 in Cardiomyocyte Differentiation. Int J Mol Sci. 2021 Apr 21;22(9):4346. doi: 10.3390/ijms22094346.
12. Taheri S, Karaca Z, Rassoulzadegan M, Mehmetbeyoglu E, Zararsiz G, Sener EF, Bayram KK, Tufan E, Sahin MC, Marasli MK, Memis M, Canatan H, Ozturk F, Tanriverdi F, Unluhizarci K, Kelestimur F. The Characterization of Sex Differences in Hypoglycemia-Induced Activation of HPA Axis on the Transcriptomic Level. Cell Mol Neurobiol. 2022 Jul;42(5):1523-1542. doi: 10.1007/s10571-021-01043-0.
13. Ozkul Y, Taheri S, Bayram KK, Sener EF, Mehmetbeyoglu E, Öztop DB, Aybuga F, Tufan E, Bayram A, Dolu N, Zararsiz G, Kianmehr L, Beyaz F, Doganyigit Z, Cuzin F, Rassoulzadegan M. A heritable profile of six miRNAs in autistic patients and mouse models. Sci Rep. 2020 Jun 9;10(1):9011. doi: 10.1038/s41598-020-65847-8.
14. Rassoulzadegan M, Ala F, Jazebi M, Enayat MS, Tabibian S, Shams M, Bahraini M, Dorgalaleh A. Molecular and clinical profile of type 2 von Willebrand disease in Iran: a thirteen-year experience. Int J Hematol. 2020 Apr;111(4):535-543. doi: 10.1007/s12185-019-02814-8.
15. Kianmehr L, Khazali H, Rajabi-Maham H, Sharifi-Zarchi A, Cuzin F, Rassoulzadegan M. Genome-Wide Distribution of Nascent Transcripts in Sperm DNA, Products of a Late Wave of General Transcription. Cells. 2019 Oct 3;8(10):1196. doi: 10.3390/cells8101196.
16. Lopez P, Yaman R, Lopez-Fernandez LA, Vidal F, Puel D, Clertant P, Cuzin F, Rassoulzadegan M. Withdrawal: A novel germ line-specific gene of the phosducin-like protein (PhLP) family: A meiotic function conserved from yeast to mice. J Biol Chem. 2019 Sep 13;294(37):13832. doi: 10.1074/jbc.W119.010673.
17. Ghassemi B, Ajami M, Shamsara M, Soleimani M, Kiani J, Rassoulzadegan M. Corrigendum to “Pipeline for the generation of gene knockout mice using dual sgRNA CRISPR/Cas9-mediated gene editing”[Anal. Biochem. 568 (2019) 31-40]. Anal Biochem. 2019 Oct 15;583:113343. doi: 10.1016/j.ab.2019.113343.
18. Bohacek J, Rassoulzadegan M. Sperm RNA: Quo vadis? Semin Cell Dev Biol. 2020 Jan;97:123-130. doi: 10.1016/j.semcdb.2019.07.005.
19. Zhang Y, Shi J, Rassoulzadegan M, Tuorto F, Chen Q. Sperm RNA code programmes the metabolic health of offspring. Nat Rev Endocrinol. 2019 Aug;15(8):489-498. doi: 10.1038/s41574-019-0226-2.
20. Vidal F, Lopez P, Lopez-Fernandez LA, Ranc F, Scimeca JC, Cuzin F, Rassoulzadegan M. Expression of Concern: Gene trap analysis of germ cell signaling to Sertoli cells: NGF-TrkA mediated induction of Fra1 and Fos by post-meiotic germ cells. J Cell Sci. 2019 May 15;132(10):jcs233692. doi: 10.1242/jcs.233692.
21. Ghassemi B, Shamsara M, Soleimani M, Kiani J, Rassoulzadegan M. Pipeline for the generation of gene knockout mice using dual sgRNA CRISPR/Cas9-mediated gene editing. Anal Biochem. 2019 Mar 1;568:31-40. doi: 10.1016/j.ab.2018.12.002.
22. Rassoulzadegan M, Cuzin F. Nutrition meets heredity: a case of RNA-mediated transmission of acquired characters. Environ Epigenet. 2018 Apr 26;4(2):dvy006. doi: 10.1093/eep/dvy006.
23. Kohram F, Fallah P, Shamsara M, Bolandi Z, Rassoulzadegan M, Soleimani M, Ghanbarian H. Cell type-dependent functions of microRNA-92a. J Cell Biochem. 2018 Jul;119(7):5798-5804. doi: 10.1002/jcb.26765.
24. Niavarani A, Shahrabi Farahani A, Sharafkhah M, Rassoulzadegan M. Pancancer analysis identifies prognostic high-APOBEC1 expression level implicated in cancer in-frame insertions and deletions. Carcinogenesis. 2018 Mar 8;39(3):327-335. doi: 10.1093/carcin/bgy005.
25. Druelle N, Vieira A, Shabro A, Courtney M, Mondin M, Rekima S, Napolitano T, Silvano S, Navarro-Sanz S, Hadzic B, Avolio F, Rassoulzadegan M, Schmid HA, Mansouri A, Collombat P. Ectopic expression of Pax4 in pancreatic δ cells results in β-like cell neogenesis. J Cell Biol. 2017 Dec 4;216(12):4299-4311. doi: 10.1083/jcb.201704044.
26. Capovilla M, Robichon A, Rassoulzadegan M. A new paramutation-like example at the Delta gene of Drosophila. PLoS One. 2017 Mar 29;12(3):e0172780. doi: 10.1371/journal.pone.0172780.
27. Ghanbarian H, Wagner N, Michiels JF, Cuzin F, Wagner KD, Rassoulzadegan M. Small RNA-directed epigenetic programming of embryonic stem cell cardiac differentiation. Sci Rep. 2017 Feb 6;7:41799. doi: 10.1038/srep41799.
28. Ghanbarian H, Wagner N, Polo B, Baudouy D, Kiani J, Michiels JF, Cuzin F, Rassoulzadegan M, Wagner KD. Dnmt2/Trdmt1 as Mediator of RNA Polymerase II Transcriptional Activity in Cardiac Growth. PLoS One. 2016 Jun 6;11(6):e0156953. doi: 10.1371/journal.pone.0156953.
29. Grandjean V, Fourré S, De Abreu DA, Derieppe MA, Remy JJ, Rassoulzadegan M. RNA-mediated paternal heredity of diet-induced obesity and metabolic disorders. Sci Rep. 2015 Dec 14;5:18193. doi: 10.1038/srep18193.
30. Rassoulzadegan M, Cuzin F. From paramutation to human disease: RNA-mediated heredity. Semin Cell Dev Biol. 2015 Aug;44:47-50. doi: 10.1016/j.semcdb.2015.08.007.
31. Rassoulzadegan M, Cuzin F. Epigenetic heredity: RNA-mediated modes of phenotypic variation. Ann N Y Acad Sci. 2015 Apr;1341:172-5. doi: 10.1111/nyas.12694.
32. Liebers R, Rassoulzadegan M, Lyko F. Epigenetic regulation by heritable RNA. PLoS Genet. 2014 Apr 17;10(4):e1004296. doi: 10.1371/journal.pgen.1004296.
33. Kiani J, Grandjean V, Liebers R, Tuorto F, Ghanbarian H, Lyko F, Cuzin F, Rassoulzadegan M. RNA-mediated epigenetic heredity requires the cytosine methyltransferase Dnmt2. PLoS Genet. 2013 May;9(5):e1003498. doi: 10.1371/journal.pgen.1003498.
34. Enayat MS, Ravanbod S, Rassoulzadegan M, Jazebi M, Ala F, Budde U, Schneppenheim S, Obser T, Schneppenheim R. Identification of a homozygous Cys410Ser mutation in the von Willebrand factor D2 domain causing type 2A(IIC) von Willebrand disease phenotype in an Iranian patient. Haemophilia. 2013 Jul;19(4):e261-4. doi: 10.1111/hae.12161.
35. Kiani J, Rassoulzadegan M. A load of small RNAs in the sperm – how many bits of hereditary information? Cell Res. 2013 Jan;23(1):18-9. doi: 10.1038/cr.2012.181.
36. Enayat S, Ravanbod S, Rassoulzadegan M, Jazebi M, Tarighat S, Ala F, Emsley J, Othman M. A novel D235Y mutation in the GP1BA gene enhances platelet interaction with von Willebrand factor in an Iranian family with platelet-type von Willebrand disease. Thromb Haemost. 2012 Nov;108(5):946-54. doi: 10.1160/TH12-04-0189.
37. Kawano M, Kawaji H, Grandjean V, Kiani J, Rassoulzadegan M. Novel small noncoding RNAs in mouse spermatozoa, zygotes and early embryos. PLoS One. 2012;7(9):e44542. doi: 10.1371/journal.pone.0044542.
38. Ghanbarian H, Grandjean V, Cuzin F, Rassoulzadegan M. A Network of Regulations by Small Non-Coding RNAs: The P-TEFb Kinase in Development and Pathology. Front Genet. 2011 Dec 28;2:95. doi: 10.3389/fgene.2011.00095.
39. Ravanbod S, Rassoulzadegan M, Rastegar-Lari G, Jazebi M, Enayat S, Ala F. Identification of 123 previously unreported mutations in the F8 gene of Iranian patients with haemophilia A. Haemophilia. 2012 May;18(3):e340-6. doi: 10.1111/j.1365-2516.2011.02708.x.
40. Keber R, Motaln H, Wagner KD, Debeljak N, Rassoulzadegan M, Ačimovič  J, Rozman D, Horvat S. Mouse knockout of the cholesterogenic cytochrome P450 lanosterol 14alpha-demethylase (Cyp51) resembles Antley-Bixler syndrome. J Biol Chem. 2011 Aug 19;286(33):29086-29097. doi: 10.1074/jbc.M111.253245.
41. Rafati M, Ravanbod S, Hoseini A, Rassoulzadegan M, Jazebi M, Enayat MS, Ala FA, Ghaffari SR. Identification of ten large deletions and one duplication in the F8 gene of eleven unrelated Iranian severe haemophilia A families using the multiplex ligation-dependent probe amplification technique. Haemophilia. 2011 Jul;17(4):705-7. doi: 10.1111/j.1365-2516.2010.02476.x.
42. Cuzin F, Rassoulzadegan M. Non-Mendelian epigenetic heredity: gametic RNAs as epigenetic regulators and transgenerational signals. Essays Biochem. 2010 Sep 20;48(1):101-6. doi: 10.1042/bse0480101.
43. Rassoulzadegan M, Cuzin F. The making of an organ: RNA mediated developmental controls in mice. Organogenesis. 2010 Jan-Mar;6(1):33-6. doi: 10.4161/org.6.1.11094.
44. Grandjean V, Gounon P, Wagner N, Martin L, Wagner KD, Bernex F, Cuzin F, Rassoulzadegan M. The miR-124-Sox9 paramutation: RNA-mediated epigenetic control of embryonic and adult growth. Development. 2009 Nov;136(21):3647-55. doi: 10.1242/dev.041061.
45. Grandjean V, Rassoulzadegan M. Epigénétique du spermatozoïde: un rôle inattendu de l’ARN [Epigenetic inheritance of the sperm: an unexpected role of RNA]. Gynecol Obstet Fertil. 2009 Jun;37(6):558-61. French. doi: 10.1016/j.gyobfe.2009.04.005.
46. Rassoulzadegan M. A response to ‘Mammalian paramutation: a tail’s tale?’–a commentary by H. Arnheiter on our paramutation paper. Pigment Cell Melanoma Res. 2009 Feb;22(1):140-1; author reply 142-3. doi: 10.1111/j.1755-148X.2008.00521.x.