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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2006 1
2008 1
2009 3
2010 2
2011 1
2012 5
2013 1
2014 2
2015 4
2016 5
2017 2
2019 1
2020 3
2021 1
2022 1
2023 3
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30 results

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Page 1
Human cerebral organoids - a new tool for clinical neurology research.
Eichmüller OL, Knoblich JA. Eichmüller OL, et al. Nat Rev Neurol. 2022 Nov;18(11):661-680. doi: 10.1038/s41582-022-00723-9. Epub 2022 Oct 17. Nat Rev Neurol. 2022. PMID: 36253568 Free PMC article. Review.
We discuss different methodologies for producing organoids and how organoids can be and have been used to model neurological disorders, including microcephaly, Zika virus infection, Alzheimer disease and other neurodegenerative disorders, and neurodevelopmental diseases, such as …
We discuss different methodologies for producing organoids and how organoids can be and have been used to model neurological disorders, incl …
CACNA1C-Related Channelopathies.
Herold KG, Hussey JW, Dick IE. Herold KG, et al. Handb Exp Pharmacol. 2023;279:159-181. doi: 10.1007/164_2022_624. Handb Exp Pharmacol. 2023. PMID: 36598608 Free PMC article. Review.
The first mutations identified within CACNA1C were shown to cause a severe, multisystem disorder known as Timothy syndrome (TS), which is characterized by neurodevelopmental deficits, long-QT syndrome, life-threatening cardiac arrhythmias, craniofacial abnormalities …
The first mutations identified within CACNA1C were shown to cause a severe, multisystem disorder known as Timothy syndrome (TS …
Timothy syndrome iPSC modeling.
Bekdash R, Klein AD, Yazawa M. Bekdash R, et al. Mol Cell Neurosci. 2020 Sep;107:103529. doi: 10.1016/j.mcn.2020.103529. Epub 2020 Jul 3. Mol Cell Neurosci. 2020. PMID: 32629111 Review.
Particular gain-of-function mutations in CACNA1C encoding Ca(V)1.2 have been associated with Timothy Syndrome, a devastating disease with a multi-organ phenotype. Efforts to understand the underlying pathophysiology and find therapeutic strategy have been spurred re …
Particular gain-of-function mutations in CACNA1C encoding Ca(V)1.2 have been associated with Timothy Syndrome, a devastating d …
Current updates on arrhythmia within Timothy syndrome: genetics, mechanisms and therapeutics.
Jiang C, Zhang Y. Jiang C, et al. Expert Rev Mol Med. 2023 May 3;25:e17. doi: 10.1017/erm.2023.11. Expert Rev Mol Med. 2023. PMID: 37132248 Free PMC article. Review.
Timothy syndrome (TS), characterised by multiple system malfunction especially the prolonged corrected QT interval and synchronised appearance of hand/foot syndactyly, is an extremely rare disease affecting early life with devastating arrhythmia. ...
Timothy syndrome (TS), characterised by multiple system malfunction especially the prolonged corrected QT interval and synchro …
Syndromic forms of congenital hyperinsulinism.
Zenker M, Mohnike K, Palm K. Zenker M, et al. Front Endocrinol (Lausanne). 2023 Mar 30;14:1013874. doi: 10.3389/fendo.2023.1013874. eCollection 2023. Front Endocrinol (Lausanne). 2023. PMID: 37065762 Free PMC article. Review.
Turner, Kabuki, and Costello syndromes), congenital disorders of glycosylation, and syndromic channelopathies (e.g. Timothy syndrome). This article reviews syndromic conditions that have been asserted by the literature to be associated with CHI. ...
Turner, Kabuki, and Costello syndromes), congenital disorders of glycosylation, and syndromic channelopathies (e.g. Timothy syndro …
Voltage-Gated Calcium Channels in Nonexcitable Tissues.
Pitt GS, Matsui M, Cao C. Pitt GS, et al. Annu Rev Physiol. 2021 Feb 10;83:183-203. doi: 10.1146/annurev-physiol-031620-091043. Epub 2020 Oct 26. Annu Rev Physiol. 2021. PMID: 33106102 Free PMC article. Review.
The identification of a gain-of-function mutation in CACNA1C as the cause of Timothy syndrome, a rare disorder characterized by cardiac arrhythmias and syndactyly, highlighted roles for the L-type voltage-gated Ca(2+) channel Ca(V)1.2 in nonexcitable cells. ...
The identification of a gain-of-function mutation in CACNA1C as the cause of Timothy syndrome, a rare disorder characterized b …
L-type Ca2+ channel function during Timothy syndrome.
Dixon RE, Cheng EP, Mercado JL, Santana LF. Dixon RE, et al. Trends Cardiovasc Med. 2012 Apr;22(3):72-6. doi: 10.1016/j.tcm.2012.06.015. Trends Cardiovasc Med. 2012. PMID: 22999068 Free PMC article. Review.
Two de novo point mutations of Ca(v)1.2 glycine residues, G406R and G402S, cause a rare multisystem disorder called Timothy syndrome (TS). Here, we discuss recent work on the mechanisms by which Ca(v)1.2 channels bearing TS mutations display slowed inactivation that …
Two de novo point mutations of Ca(v)1.2 glycine residues, G406R and G402S, cause a rare multisystem disorder called Timothy syndro …
Genetics of long QT syndrome.
Tester DJ, Ackerman MJ. Tester DJ, et al. Methodist Debakey Cardiovasc J. 2014 Jan-Mar;10(1):29-33. doi: 10.14797/mdcj-10-1-29. Methodist Debakey Cardiovasc J. 2014. PMID: 24932360 Free PMC article. Review.
In addition, three atypical LQTS or multisystem syndromic disorders that have been associated with QT prolongation have been described, including ankyrin-B syndrome, Anderson-Tawil syndrome (ATS), and Timothy syndrome (TS). Genetic testing for LQTS is recommended in …
In addition, three atypical LQTS or multisystem syndromic disorders that have been associated with QT prolongation have been described, incl …
Cav1.2 channelopathies causing autism: new hallmarks on Timothy syndrome.
Marcantoni A, Calorio C, Hidisoglu E, Chiantia G, Carbone E. Marcantoni A, et al. Pflugers Arch. 2020 Jul;472(7):775-789. doi: 10.1007/s00424-020-02430-0. Epub 2020 Jul 3. Pflugers Arch. 2020. PMID: 32621084 Free article. Review.
De novo mutations in the gene encoding Cav1.2 (CACNA1C) causes two forms of Timothy syndrome (TS1, TS2), characterized by a multisystem disorder inclusive of cardiac arrhythmias, long QT, autism, and adrenal gland dysfunction. ...
De novo mutations in the gene encoding Cav1.2 (CACNA1C) causes two forms of Timothy syndrome (TS1, TS2), characterized by a mu …
Modeling psychiatric disorders with patient-derived iPSCs.
Wen Z, Christian KM, Song H, Ming GL. Wen Z, et al. Curr Opin Neurobiol. 2016 Feb;36:118-27. doi: 10.1016/j.conb.2015.11.003. Epub 2015 Dec 17. Curr Opin Neurobiol. 2016. PMID: 26705693 Free PMC article. Review.
30 results