Emerging Role of <i>ODC1</i> in Neurodevelopmental Disorders and Brain Development
Ornithine decarboxylase 1 (<i>ODC1</i> gene) has been linked through gain-of-function variants to a rare disease featuring developmental delay, alopecia, macrocephaly, and structural brain anomalies. <i>ODC1</i> has been linked to additional diseases like cancer, with growing...
Main Authors: | Jeremy W. Prokop, Caleb P. Bupp, Austin Frisch, Stephanie M. Bilinovich, Daniel B. Campbell, Daniel Vogt, Chad R. Schultz, Katie L. Uhl, Elizabeth VanSickle, Surender Rajasekaran, André S. Bachmann |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2021-03-01
|
Series: | Genes |
Subjects: | |
Online Access: | https://www.mdpi.com/2073-4425/12/4/470 |
Similar Items
-
The ODC 3′-Untranslated Region and 5′-Untranslated Region Contain cis-Regulatory Elements: Implications for Carcinogenesis
by: Shannon L. Nowotarski, et al.
Published: (2017-12-01) -
Effects of ODC on polyamine metabolism, hormone levels, cell proliferation and apoptosis in goose ovarian granulosa cells
by: Chunyang Niu, et al.
Published: (2021-08-01) -
Plasmodium AdoMetDC/ODC bifunctional enzyme is essential for male sexual stage development and mosquito transmission
by: Robert J. Hart, et al.
Published: (2016-08-01) -
Polyamine Biosynthetic Pathway as a Drug Target for Osteosarcoma Therapy
by: Rebecca R. Weicht, et al.
Published: (2018-08-01) -
Investigation on Ornithine Decarboxylase Activity and Level of Putrescine, Spermidine and Spermine in Hydatid Cyst
by: Somayeh Bahrami, et al.
Published: (2017-01-01)