Cargando…
Deleterious mutations in ALDH1L2 suggest a novel cause for neuro-ichthyotic syndrome
Neuro-ichthyotic syndromes are a group of rare genetic diseases mainly associated with perturbations in lipid metabolism, intracellular vesicle trafficking, or glycoprotein synthesis. Here, we report a patient with a neuro-ichthyotic syndrome associated with deleterious mutations in the ALDH1L2 (ald...
Autores principales: | Sarret, Catherine, Ashkavand, Zahra, Paules, Evan, Dorboz, Imen, Pediaditakis, Peter, Sumner, Susan, Eymard-Pierre, Eléonore, Francannet, Christine, Krupenko, Natalia I., Boespflug-Tanguy, Odile, Krupenko, Sergey A. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6650503/ https://www.ncbi.nlm.nih.gov/pubmed/31341639 http://dx.doi.org/10.1038/s41525-019-0092-9 |
Ejemplares similares
-
CHIP E3 ligase mediates proteasomal degradation of the proliferation regulatory protein ALDH1L1 during the transition of NIH3T3 fibroblasts from G(0)/G(1) to S-phase
por: Khan, Qasim A., et al.
Publicado: (2018) -
Aldh1l2 knockout mouse metabolomics links the loss of the mitochondrial folate enzyme to deregulation of a lipid metabolism observed in rare human disorder
por: Krupenko, Natalia I., et al.
Publicado: (2020) -
Knockout of Putative Tumor Suppressor Aldh1l1 in Mice Reprograms Metabolism to Accelerate Growth of Tumors in a Diethylnitrosamine (DEN) Model of Liver Carcinogenesis
por: Krupenko, Natalia I., et al.
Publicado: (2021) -
Neuro-ichthyotic Syndromes: A Case Series
por: Incecık, Faruk, et al.
Publicado: (2018) -
Structure of putative tumor suppressor ALDH1L1
por: Tsybovsky, Yaroslav, et al.
Publicado: (2022)