All Relations between Autism Spectrum Disorder and Hydrocephalus
| Publication | Sentence | Publish Date | Extraction Date | Species |
|---|---|---|---|---|
| Melinda Moseley-Alldredge, Caroline Aragón, Marcus Vargus, Divya Alley, Nirali Somia, Lihsia Che. The L1CAM SAX-7 is an antagonistic modulator of Erk Signaling. bioRxiv : the preprint server for biology. 2024-09-30. PMID:39345534. | in addition to being associated with the autism and schizophrenia spectrum disorders, mutations in the l1cam family of genes also underlie distinct developmental syndromes with neurological conditions, such as intellectual disability, spastic paraplegia, hypotonia and congenital hydrocephalus. | 2024-09-30 | 2024-10-02 | Not clear |
| Videep Soni, Joseph J LoTurc. KATNAL2 mutations link ciliary dysfunction to hydrocephalus and autism. Proceedings of the National Academy of Sciences of the United States of America. vol 121. issue 30. 2024-07-15. PMID:39008680. | katnal2 mutations link ciliary dysfunction to hydrocephalus and autism. | 2024-07-15 | 2024-07-18 | Not clear |
| Melinda Moseley-Alldredge, Seema Sheoran, Hayoung Yoo, Calvin O'Keefe, Janet E Richmond, Lihsia Che. A role for the Erk MAPK pathway in modulating SAX-7/L1CAM-dependent locomotion in Caenorhabditis elegans. Genetics. 2021-12-01. PMID:34849872. | besides being associated with autism and schizophrenia spectrum disorders, impaired l1cam function also underlies the x-linked l1 syndrome, which encompasses a group of neurological conditions, including spastic paraplegia and congenital hydrocephalus. | 2021-12-01 | 2023-08-13 | caenorhabditis_elegans |
| Tyrone DeSpenza, Marina Carlson, Shreyas Panchagnula, Stephanie Robert, Phan Q Duy, Nell Mermin-Bunnell, Benjamin C Reeves, Adam Kundishora, Aladine A Elsamadicy, Hannah Smith, Jack Ocken, Seth L Alper, Sheng Chih Jin, Ellen J Hoffman, Kristopher T Kahl. PTEN mutations in autism spectrum disorder and congenital hydrocephalus: developmental pleiotropy and therapeutic targets. Trends in neurosciences. vol 44. issue 12. 2021-11-25. PMID:34625286. | pten mutations in autism spectrum disorder and congenital hydrocephalus: developmental pleiotropy and therapeutic targets. | 2021-11-25 | 2023-08-13 | human |