Francois Cuzin
Overview
Explore the profile of Francois Cuzin including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
29
Citations
874
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Yilmaz Sukranli Z, Bayram K, Taheri S, Cuzin F, Ozkul Y, Rassoulzadegan M
Sci Rep
. 2024 Aug;
14(1):19014.
PMID: 39152124
We previously identified a unique genetic feature of Autism Spectrum Disorder (ASD) in human patients and established mouse models, a low to very low level of six microRNAs, miR-19a-3p, miR-361-5p,...
2.
Ozkul Y, Taheri S, Bayram K, Sener E, Mehmetbeyoglu E, Oztop D, et al.
Sci Rep
. 2020 Jun;
10(1):9011.
PMID: 32514154
Autism spectrum disorder (ASD) is a group of developmental pathologies that impair social communication and cause repetitive behaviors. The suggested roles of noncoding RNAs in pathology led us to perform...
3.
Kianmehr L, Khazali H, Rajabi-Maham H, Sharifi-Zarchi A, Cuzin F, Rassoulzadegan M
Cells
. 2019 Oct;
8(10).
PMID: 31623338
Mature spermatozoa contain a whole repertoire of the various classes of cellular RNAs, both coding and non-coding. It was hypothesized that after fertilization they might impact development, a claim supported...
4.
Lopez P, Yaman R, Lopez-Fernandez L, Vidal F, Puel D, Clertant P, et al.
J Biol Chem
. 2019 Sep;
294(37):13832.
PMID: 31519761
No abstract available.
5.
Rassoulzadegan M, Cuzin F
Environ Epigenet
. 2018 May;
4(2):dvy006.
PMID: 29732170
RNA-based inheritance provides a reasonable hypothesis to explain multigenerational maintenance of the disease in the progeny of either a male or female parent suffering from the metabolic syndrome (obesity and...
6.
Ghanbarian H, Wagner N, Michiels J, Cuzin F, Wagner K, Rassoulzadegan M
Sci Rep
. 2017 Feb;
7:41799.
PMID: 28165496
Microinjection of small noncoding RNAs in one-cell embryos was reported in several instances to result in transcriptional activation of target genes. To determine the molecular mechanisms involved and to explore...
7.
Ghanbarian H, Wagner N, Polo B, Baudouy D, Kiani J, Michiels J, et al.
PLoS One
. 2016 Jun;
11(6):e0156953.
PMID: 27270731
Dnmt2/Trdmt1 is a methyltransferase, which has been shown to methylate tRNAs. Deficient mutants were reported to exhibit various, seemingly unrelated, defects in development and RNA-mediated epigenetic heredity. Here we report...
8.
Rassoulzadegan M, Cuzin F
Semin Cell Dev Biol
. 2015 Sep;
44:47-50.
PMID: 26335266
Epigenetic variation, a stable alteration in gene expression, occurs at multiple moments during development. Several instances of non-Mendelian transmission to the progenies modes are very intriguing. Studies of the mode...
9.
Rassoulzadegan M, Cuzin F
Ann N Y Acad Sci
. 2015 Mar;
1341:172-5.
PMID: 25726734
In addition to the Mendelian mutations, several instances of heritable phenotypic variation have been reported. We have observed, in mice, a role for sperm RNAs in the induction of such...
10.