Hydrolethalus syndrome

Networked: 6 relevant articles (0 outcomes, 0 trials/studies)

1.	Hu, Jinghua: 3 articles (01/2021 - 01/2016)
2.	Dammermann, Alexander: 3 articles (01/2017 - 09/2009)
3.	Ling, Kun: 2 articles (01/2021 - 01/2016)
4.	Zhang, Yuxia: 2 articles (01/2021 - 01/2016)
5.	Wei, Qing: 2 articles (01/2020 - 01/2016)
6.	Chen, Chuan: 1 article (01/2021)
7.	Davies, Brian A: 1 article (01/2021)
8.	Harris, Peter C: 1 article (01/2021)
9.	Huang, Yan: 1 article (01/2021)
10.	Katzmann, David J: 1 article (01/2021)

Drugs and Important Biological Agents (IBA) related to Hydrolethalus syndrome:

1.	Proteins (Proteins, Gene)FDA Link 01/01/2020 - "Functional Analysis of Hydrolethalus Syndrome Protein HYLS1 in Ciliogenesis and Spermatogenesis in Drosophila." 01/01/2017 - "The hydrolethalus syndrome protein HYLS-1 is the only centriolar protein known to remain at the base of mature cilia and is required for intraflagellar transport trafficking. " 01/01/2016 - "elegans orthologue of hydrolethalus syndrome protein 1, is required for TF formation, TZ organization and ciliary gating. " 01/01/2016 - "The hydrolethalus syndrome protein HYLS-1 regulates formation of the ciliary gate." 09/01/2009 - "The hydrolethalus syndrome protein HYLS-1 links core centriole structure to cilia formation."
2.	SqualeneIBA 08/30/2004 - "Hydrolethalus syndrome, in contrast to Smith-Lemli-Opitz syndrome, is not due to a defect in post-squalene cholesterol biosynthesis: a case report."
3.	CholesterolIBA 08/30/2004 - "Hydrolethalus syndrome, in contrast to Smith-Lemli-Opitz syndrome, is not due to a defect in post-squalene cholesterol biosynthesis: a case report."
4.	Amino Acids FDA Link 09/01/2009 - "A single amino acid change in human HYLS1 leads to a perinatal lethal disorder termed hydrolethalus syndrome, and we show that this mutation impairs HYLS-1 function in ciliogenesis. "