Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Martine W. Tremblay"'
Autor:
Jonathan P. Kastan, Martine W. Tremblay, Michael C. Brown, Joseph D. Trimarco, Elena Y. Dobrikova, Mikhail I. Dobrikov, Matthias Gromeier
Publikováno v:
mBio, Vol 12, Iss 2 (2021)
It is believed that ∼7,000 messenger RNAs (mRNAs) are subject to N6
Externí odkaz:
https://doaj.org/article/eba075ab535042b3a16853b5e2479596
Autor:
Yong-hui Jiang, Martine W. Tremblay
Publikováno v:
Annual Review of Medicine. 70:151-166
The prevalence of autism spectrum disorder (ASD) has been increasing steadily over the last 20 years; however, the molecular basis for the majority of ASD cases remains unknown. Recent advances in next-generation sequencing and detection of DNA modif
Autor:
Mikhail I. Dobrikov, Joseph D. Trimarco, Michael C. Brown, Martine W. Tremblay, Elena Y. Dobrikova, Matthias Gromeier, Jonathan P. Kastan
Publikováno v:
mBio, Vol 12, Iss 2 (2021)
mBio
mBio
It is believed that ∼7,000 messenger RNAs (mRNAs) are subject to N6-methyladenosine modification. The biological significance of this remains mysterious.
Enteroviruses (EV) deploy two proteases that mediate viral polyprotein cleavage and host
Enteroviruses (EV) deploy two proteases that mediate viral polyprotein cleavage and host
Autor:
Martine W Tremblay, Matthew V Green, Jill A Rosenfeld, Haley Streff, William Craigen, Nasim Bekheirnia, Saeed Al Tala, Wendy D Tan, Anne E West, Yong-hui Jiang
Background: Rahman syndrome (RMNS) is a rare genetic disorder characterized by mild to severe intellectual disability, hypotonia, anxiety, autism spectrum disorder, vision problems, brittle bones, and dysmorphic facies. De novo heterozygous mutations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::07d8a3a2d48be5f55291ebc9854f6c5b
https://doi.org/10.21203/rs.3.rs-135774/v1
https://doi.org/10.21203/rs.3.rs-135774/v1
Autor:
Xinyu Cao, Martine W. Tremblay, Yong-hui Jiang, Lara J. Duffney, Allyn McConkie-Rosell, Purnima T. Valdez, Sarah Montgomery
Genetic mutations in genes encoding proteins involved in epigenetic machinery have been reported in individuals with autism spectrum disorder (ASD), intellectual disability, congenital heart disease, and other disorders. H1 histone linker protein, th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c61048f40968d24f24ad33b86846ad7e
https://europepmc.org/articles/PMC5980735/
https://europepmc.org/articles/PMC5980735/
Autor:
Alexandra L. Bey, Stephen K. Siecinski, Simon G. Gregory, Leeyup Chung, Wei Xie, Xinyu Cao, Aaron J. Towers, Xiangyin Kong, Xin-lei Li, Sonia Xu, Lara J. Duffney, Martine W. Tremblay, Xiaoming Wang, Ping Wang, Yong-hui Jiang, Wen-Hao Zhang, Yuna Kim
Publikováno v:
JCI insight. 3(23)
OXTR modulates a variety of behaviors in mammals, including social memory and recognition. Genetic and epigenetic dysregulation of OXTR has been suggested to be implicated in neuropsychiatric disorders, including autism spectrum disorder (ASD). While