Lysyl oxidase homolog 1, also known as LOXL1, is an enzyme which in humans is encoded by the LOXL1 gene. This gene encodes a member of the lysyl oxidase...
8 KB (1,012 words) - 02:53, 1 January 2024
has associated PEX with polymorphisms in gene LOXL1. A report suggested that a specific gene named LOXL1 which was a member of the family of enzymes which...
29 KB (3,531 words) - 20:16, 9 September 2024
Wolosin JM (July 2018). "Exfoliation syndrome: A disease of autophagy and LOXL1 proteopathy". Journal of Glaucoma. 27 (Supplement 1): S44–S53. doi:10.1097/IJG...
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HGNC:6663 P23490 8813 LOX HGNC:6664 P28300 8814 LOXHD1 HGNC:26521 Q8IVV2 8815 LOXL1 HGNC:6665 Q08397 8816 LOXL2 HGNC:6666 Q9Y4K0 8817 LOXL3 HGNC:13869 P58215...
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extracellular matrix, including neurodegenerative and cardiovascular diseases. LOXL1 LOXL2 LOXL3 LOXL4 Menkes disease Occipital horn syndrome GRCh38: Ensembl...
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September 2010; G Thorleifsson et al., "Common Sequence Variants in the LOXL1 Gene Confer Susceptibility to Exfoliation Glaucoma," Science (subscription...
103 KB (12,457 words) - 02:27, 23 October 2024
of several types of cancer and fibrotic diseases such as liver fibrosis. LOXL1 LOXL3 LOXL4 GRCh38: Ensembl release 89: ENSG00000134013 – Ensembl, May 2017...
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arthropathy (joint pathology) and vitreoretinopathy (pathology of the eye). LOXL1 LOXL2 LOXL4 GRCh38: Ensembl release 89: ENSG00000115318 – Ensembl, May 2017...
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suppression, cell growth control, and chemotaxis to each member of the family. LOXL1 LOXL2 LOXL3 GRCh38: Ensembl release 89: ENSG00000138131 – Ensembl, May 2017...
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vascular development and remodeling. FBLN5 has been shown to interact with LOXL1 and apolipoprotein(a). FBLN5 mutations have been described in patients with...
11 KB (1,401 words) - 05:00, 24 December 2023