Found: 9
Select item for more details and to access through your institution.
The UPF3B gene, implicated in intellectual disability, autism, ADHD and childhood onset schizophrenia regulates neural progenitor cell behaviour and neuronal outgrowth.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 23, p. 4673, doi. 10.1093/hmg/ddt315
- By:
- Publication type:
- Article
Disrupted Excitatory Synaptic Contacts and Altered Neuronal Network Activity Underpins the Neurological Phenotype in PCDH19-Clustering Epilepsy (PCDH19-CE).
- Published in:
- Molecular Neurobiology, 2021, v. 58, n. 5, p. 2005, doi. 10.1007/s12035-020-02242-4
- By:
- Publication type:
- Article
Transcription factor genetics and biology in predisposition to bone marrow failure and hematological malignancy.
- Published in:
- Frontiers in Oncology, 2023, p. 1, doi. 10.3389/fonc.2023.1183318
- By:
- Publication type:
- Article
Zinc and Zinc Transporters in Macrophages and Their Roles in Efferocytosis in COPD.
- Published in:
- PLoS ONE, 2014, v. 9, n. 10, p. 1, doi. 10.1371/journal.pone.0110056
- By:
- Publication type:
- Article
Pcdh19 Loss-of-Function Increases Neuronal Migration In Vitro but is Dispensable for Brain Development in Mice.
- Published in:
- Scientific Reports, 2016, p. 26765, doi. 10.1038/srep26765
- By:
- Publication type:
- Article
Cover, Volume 42, Issue 11.
- Published in:
- Human Mutation, 2021, v. 42, n. 11, p. i, doi. 10.1002/humu.24288
- By:
- Publication type:
- Article
GATA2 deficiency syndrome: A decade of discovery.
- Published in:
- Human Mutation, 2021, v. 42, n. 11, p. 1399, doi. 10.1002/humu.24271
- By:
- Publication type:
- Article
Severe neurocognitive and growth disorders due to variation in THOC2, an essential component of nuclear mRNA export machinery.
- Published in:
- Human Mutation, 2018, v. 39, n. 8, p. 1126, doi. 10.1002/humu.23557
- By:
- Publication type:
- Article
Protocadherin 19 (PCDH19) interacts with paraspeckle protein NONO to co-regulate gene expression with estrogen receptor alpha (ERα).
- Published in:
- Human Molecular Genetics, 2017, v. 26, n. 11, p. 2042, doi. 10.1093/hmg/ddx094
- By:
- Publication type:
- Article