Huang J, Sung P, Hsieh S
Front Immunol. 2025; 15():1513713.
PMID: 39850902
PMC: 11754051.
DOI: 10.3389/fimmu.2024.1513713.
Liu X, Qin H, Liu Y, Ma J, Li Y, He Y
Heliyon. 2024; 10(8):e28863.
PMID: 38638974
PMC: 11024568.
DOI: 10.1016/j.heliyon.2024.e28863.
Cavusoglu D, Ozturk G, Turkdogan D, Kurul S, Yis U, Komur M
Cerebellum. 2024; 23(5):1950-1965.
PMID: 38622473
PMC: 11489189.
DOI: 10.1007/s12311-024-01690-1.
Weeratunga S, Gormal R, Liu M, Eldershaw D, Livingstone E, Malapaka A
J Biol Chem. 2023; 300(1):105541.
PMID: 38072052
PMC: 10820826.
DOI: 10.1016/j.jbc.2023.105541.
Guo Q, Kouyama-Suzuki E, Shirai Y, Cao X, Yanagawa T, Mori T
Cells. 2023; 12(8).
PMID: 37190086
PMC: 10136522.
DOI: 10.3390/cells12081177.
loss of function differentially regulates neuronal maturation and synaptic function in human induced cortical excitatory neurons.
McSweeney D, Gabriel R, Jin K, Pang Z, Aronow B, Pak C
iScience. 2022; 25(10):105187.
PMID: 36262316
PMC: 9574418.
DOI: 10.1016/j.isci.2022.105187.
Case report: A novel mutation in a Chinese female child with microcephaly with pontine and cerebellar hypoplasia.
Xie G, Zhang Y, Yang W, Yang L, Wang R, Xu M
Front Genet. 2022; 13:856636.
PMID: 36159992
PMC: 9490368.
DOI: 10.3389/fgene.2022.856636.
Case Report: Identification of a novel missense variant in a Chinese family with MICPCH.
Zhang R, Jia P, Yao Y, Zhu F
Front Genet. 2022; 13:933785.
PMID: 36092876
PMC: 9452731.
DOI: 10.3389/fgene.2022.933785.
Bi-allelic loss-of-function variants in PPFIBP1 cause a neurodevelopmental disorder with microcephaly, epilepsy, and periventricular calcifications.
Rosenhahn E, OBrien T, Zaki M, Sorge I, Wieczorek D, Rostasy K
Am J Hum Genet. 2022; 109(8):1421-1435.
PMID: 35830857
PMC: 9388382.
DOI: 10.1016/j.ajhg.2022.06.008.
A de novo variant in CASK gene causing intellectual disability and brain hypoplasia: a case report and literature review.
Zhang Y, Nie Y, Mu Y, Zheng J, Xu X, Zhang F
Ital J Pediatr. 2022; 48(1):73.
PMID: 35550617
PMC: 9097383.
DOI: 10.1186/s13052-022-01248-z.
Dietary zinc supplementation rescues fear-based learning and synaptic function in the Tbr1 mouse model of autism spectrum disorders.
Lee K, Jung Y, Vyas Y, Skelton I, Abraham W, Hsueh Y
Mol Autism. 2022; 13(1):13.
PMID: 35303947
PMC: 8932001.
DOI: 10.1186/s13229-022-00494-6.
CASK Silence Overcomes Sorafenib Resistance of Hepatocellular Carcinoma Through Activating Apoptosis and Autophagic Cell Death.
Ding B, Bao C, Jin L, Xu L, Fan W, Lou W
Front Oncol. 2021; 11:681683.
PMID: 34249726
PMC: 8260832.
DOI: 10.3389/fonc.2021.681683.
Crosstalk among Calcium ATPases: PMCA, SERCA and SPCA in Mental Diseases.
Boczek T, Sobolczyk M, Mackiewicz J, Lisek M, Ferenc B, Guo F
Int J Mol Sci. 2021; 22(6).
PMID: 33801794
PMC: 8000800.
DOI: 10.3390/ijms22062785.
Cask methylation involved in the injury of insulin secretion function caused by interleukin1-β.
Wang T, Liu X, Xie J, Yuan Q, Wang Y
J Cell Mol Med. 2020; 24(24):14247-14256.
PMID: 33188567
PMC: 7753871.
DOI: 10.1111/jcmm.16041.
Effect of Transgenesis on mRNA and miRNA Profiles in Cucumber Fruits Expressing .
Pawelkowicz M, Skarzynska A, Sroka M, Szwacka M, Pniewski T, Plader W
Genes (Basel). 2020; 11(3).
PMID: 32245082
PMC: 7140888.
DOI: 10.3390/genes11030334.
Functional characterization of TBR1 variants in neurodevelopmental disorder.
den Hoed J, Sollis E, Venselaar H, Estruch S, Deriziotis P, Fisher S
Sci Rep. 2018; 8(1):14279.
PMID: 30250039
PMC: 6155134.
DOI: 10.1038/s41598-018-32053-6.
Novel CASK mutations in cases with syndromic microcephaly.
Cristofoli F, Devriendt K, Davis E, Van Esch H, Vermeesch J
Hum Mutat. 2018; 39(7):993-1001.
PMID: 29691940
PMC: 5995665.
DOI: 10.1002/humu.23536.
Calcium/calmodulin-dependent serine protein kinase (CASK), a protein implicated in mental retardation and autism-spectrum disorders, interacts with T-Brain-1 (TBR1) to control extinction of associative memory in male mice.
Huang T, Hsueh Y
J Psychiatry Neurosci. 2017; 42(1):37-47.
PMID: 28234597
PMC: 5373711.
DOI: 10.1503/jpn.150359.
Sumoylation in Synaptic Function and Dysfunction.
Schorova L, Martin S
Front Synaptic Neurosci. 2016; 8:9.
PMID: 27199730
PMC: 4848311.
DOI: 10.3389/fnsyn.2016.00009.
The Involvement of Neuron-Specific Factors in Dendritic Spinogenesis: Molecular Regulation and Association with Neurological Disorders.
Hu H, Shih P, Shih Y, Hsueh Y
Neural Plast. 2016; 2016:5136286.
PMID: 26819769
PMC: 4706964.
DOI: 10.1155/2016/5136286.