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Year | Number of Results |
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2010 | 1 |
2018 | 1 |
2019 | 1 |
2023 | 1 |
2024 | 1 |
PubMed (GeneRIF) for id: 57685
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Biallelic loss-of-function variants in CACHD1 cause a novel neurodevelopmental syndrome with facial dysmorphism and multisystem congenital abnormalities.
Genet Med. 2024 Apr;26(4):101057. doi: 10.1016/j.gim.2023.101057. Epub 2023 Dec 27.
Genet Med. 2024.
PMID: 38158856
Free article.
CACHD1: A new activity-modifying protein for voltage-gated calcium channels.
Stephens GJ, Cottrell GS.
Stephens GJ, et al.
Channels (Austin). 2019 Dec;13(1):120-123. doi: 10.1080/19336950.2019.1600968.
Channels (Austin). 2019.
PMID: 30983497
Free PMC article.
No abstract available.
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CACHD1 is an α2δ-Like Protein That Modulates CaV3 Voltage-Gated Calcium Channel Activity.
Cottrell GS, Soubrane CH, Hounshell JA, Lin H, Owenson V, Rigby M, Cox PJ, Barker BS, Ottolini M, Ince S, Bauer CC, Perez-Reyes E, Patel MK, Stevens EB, Stephens GJ.
Cottrell GS, et al.
J Neurosci. 2018 Oct 24;38(43):9186-9201. doi: 10.1523/JNEUROSCI.3572-15.2018. Epub 2018 Sep 4.
J Neurosci. 2018.
PMID: 30181139
Free PMC article.
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Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.
Rose JE, Behm FM, Drgon T, Johnson C, Uhl GR.
Rose JE, et al.
Mol Med. 2010 Jul-Aug;16(7-8):247-53. doi: 10.2119/molmed.2009.00159. Epub 2010 Mar 17.
Mol Med. 2010.
PMID: 20379614
Free PMC article.
Clinical Trial.
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