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Page 1
Human genome meeting 2016 : Houston, TX, USA. 28 February - 2 March 2016.
Srivastava AK, Wang Y, Huang R, Skinner C, Thompson T, Pollard L, Wood T, Luo F, Stevenson R, Polimanti R, Gelernter J, Lin X, Lim IY, Wu Y, Teh AL, Chen L, Aris IM, Soh SE, Tint MT, MacIsaac JL, Yap F, Kwek K, Saw SM, Kobor MS, Meaney MJ, Godfrey KM, Chong YS, Holbrook JD, Lee YS, Gluckman PD, Karnani N; GUSTO study group; Kapoor A, Lee D, Chakravarti A, Maercker C, Graf F, Boutros M, Stamoulis G, Santoni F, Makrythanasis P, Letourneau A, Guipponi M, Panousis N, Garieri M, Ribaux P, Falconnet E, Borel C, Antonarakis SE, Kumar S, Curran J, Blangero J, Chatterjee S, Kapoor A, Akiyama J, Auer D, Berrios C, Pennacchio L, Chakravarti A, Donti TR, Cappuccio G, Miller M, Atwal P, Kennedy A, Cardon A, Bacino C, Emrick L, Hertecant J, Baumer F, Porter B, Bainbridge M, Bonnen P, Graham B, Sutton R, Sun Q, Elsea S, Hu Z, Wang P, Zhu Y, Zhao J, Xiong M, Bennett DA, Hidalgo-Miranda A, Romero-Cordoba S, Rodriguez-Cuevas S, Rebollar-Vega R, Tagliabue E, Iorio M, D’Ippolito E, Baroni S, Kaczkowski B, Tanaka Y, Kawaji H, Sandelin A, Andersson R, Itoh M, Lassmann T; The FANTOM5 Consortium; Hayashizaki Y, Carninci P, Forrest ARR, Semple CA, Rosenthal EA, Shirts B, Amendola L, Gallego C, Horike-Pyne… See abstract for full author list ➔ Srivastava AK, et al. Hum Genomics. 2016 May 26;10 Suppl 1(Suppl 1):12. doi: 10.1186/s40246-016-0063-5. Hum Genomics. 2016. PMID: 27294413 Free PMC article.
O1 The metabolomics approach to autism: identification of biomarkers for early detection of autism spectrum disorder A. ...Hu, P. Wang, Y. Zhu, J. Zhao, M. Xiong, David A Bennett O11 A microRNA signature identifies subtypes of triple-negative breast ca …
O1 The metabolomics approach to autism: identification of biomarkers for early detection of autism spectrum disorder A. …
The role of microRNAs in the molecular link between circadian rhythm and autism spectrum disorder.
Kim JY, Kim W, Lee KH. Kim JY, et al. Anim Cells Syst (Seoul). 2023 Feb 23;27(1):38-52. doi: 10.1080/19768354.2023.2180535. eCollection 2023. Anim Cells Syst (Seoul). 2023. PMID: 36860270 Free PMC article. Review.
If the circadian rhythm is abnormal, sleep disorders, such as insomnia and several other diseases, can occur. The term 'autism spectrum disorder (ASD)' is used to characterize people who exhibit a certain set of repetitive behaviors, severely constrained interests, …
If the circadian rhythm is abnormal, sleep disorders, such as insomnia and several other diseases, can occur. The term 'autism spectr …
On-going consequences of in utero exposure of Pb: An epigenetic perspective.
Tasin FR, Ahmed A, Halder D, Mandal C. Tasin FR, et al. J Appl Toxicol. 2022 Oct;42(10):1553-1569. doi: 10.1002/jat.4287. Epub 2022 Jan 24. J Appl Toxicol. 2022. PMID: 35023172 Review.
Apart from these, down-regulation and up-regulation of certain microRNAs crucial for fetal development have been shown to be associated with in utero Pb exposure in human placenta samples. All these modifications in the developing fetus during the prenatal and perinatal st …
Apart from these, down-regulation and up-regulation of certain microRNAs crucial for fetal development have been shown to be associat …
MeCP2 caught moonlighting as a suppressor of MicroRNA processing.
Woo JS, Kim VN. Woo JS, et al. Dev Cell. 2014 Mar 10;28(5):477-8. doi: 10.1016/j.devcel.2014.02.015. Dev Cell. 2014. PMID: 24636253 Free article.
MeCP2 is a transcriptional regulator important for neurodevelopment and is involved in Rett syndrome and autism. In this issue of Developmental Cell, Cheng and colleagues (2014) report that MeCP2 also regulates microRNA biogenesis. MeCP2 phosphorylation induces a di …
MeCP2 is a transcriptional regulator important for neurodevelopment and is involved in Rett syndrome and autism. In this issue of Dev …
Maternal immune activation alters brain microRNA expression in mouse offspring.
Sunwoo JS, Jeon D, Lee ST, Moon J, Yu JS, Park DK, Bae JY, Lee DY, Kim S, Jung KH, Park KI, Jung KY, Kim M, Lee SK, Chu K. Sunwoo JS, et al. Ann Clin Transl Neurol. 2018 Sep 19;5(10):1264-1276. doi: 10.1002/acn3.652. eCollection 2018 Oct. Ann Clin Transl Neurol. 2018. PMID: 30349861 Free PMC article.
OBJECTIVE: Maternal immune activation (MIA) is associated with an increased risk of autism spectrum disorder (ASD) in offspring. Herein, we investigate the altered expression of microRNAs (miRNA), and that of their target genes, in the brains of MIA mouse off …
OBJECTIVE: Maternal immune activation (MIA) is associated with an increased risk of autism spectrum disorder (ASD) in offsprin …
Post-transcriptional regulation of SHANK3 expression by microRNAs related to multiple neuropsychiatric disorders.
Choi SY, Pang K, Kim JY, Ryu JR, Kang H, Liu Z, Kim WK, Sun W, Kim H, Han K. Choi SY, et al. Mol Brain. 2015 Nov 16;8(1):74. doi: 10.1186/s13041-015-0165-3. Mol Brain. 2015. PMID: 26572867 Free PMC article.
The SHANK3 gene encoding core scaffolding proteins at glutamatergic postsynapse is a typical dosage-sensitive gene, both deletions and duplications of which are associated with Phelan-McDermid syndrome, autism spectrum disorders, bipolar disorder, intellectual disab …
The SHANK3 gene encoding core scaffolding proteins at glutamatergic postsynapse is a typical dosage-sensitive gene, both deletions and dupli …
An atypical 12q24.31 microdeletion implicates six genes including a histone demethylase KDM2B and a histone methyltransferase SETD1B in syndromic intellectual disability.
Labonne JD, Lee KH, Iwase S, Kong IK, Diamond MP, Layman LC, Kim CH, Kim HG. Labonne JD, et al. Hum Genet. 2016 Jul;135(7):757-71. doi: 10.1007/s00439-016-1668-4. Epub 2016 Apr 22. Hum Genet. 2016. PMID: 27106595
Microdeletion syndromes are frequent causes of neuropsychiatric disorders leading to intellectual disability as well as autistic features accompanied by epilepsy and craniofacial anomalies. ...The four additional candidate genes (ORAI1, MORN3, TMEM120B, RHOF), a microRN …
Microdeletion syndromes are frequent causes of neuropsychiatric disorders leading to intellectual disability as well as autistic feat …