[HTML][HTML] Established and Evolving Roles of the Multifunctional Non-POU Domain-Containing Octamer-Binding Protein (NonO) and Splicing Factor Proline-and …
D Yu, CJ Huang, HO Tucker - Journal of Developmental Biology, 2024 - mdpi.com
It has been more than three decades since the discovery of multifunctional factors, the Non-
POU-Domain-Containing Octamer-Binding Protein, NonO, and the Splicing Factor Proline …
POU-Domain-Containing Octamer-Binding Protein, NonO, and the Splicing Factor Proline …
[HTML][HTML] Case Report: Non-ossifying fibromas with pathologic fractures in a patient with NONO-associated X-linked syndromic intellectual developmental disorder
The NONO gene encodes a nuclear protein involved in transcriptional regulation, RNA
synthesis and DNA repair. Hemizygous loss-of function, de novo or maternally inherited …
synthesis and DNA repair. Hemizygous loss-of function, de novo or maternally inherited …
[HTML][HTML] X-linked intellectual developmental disorder with onset of neonatal heart failure: A case report and literature review
H Xi, L Ma, X Yin, P Yang, X Li, L Li - Molecular Genetics and Metabolism …, 2024 - Elsevier
X-linked intellectual developmental disorder is a rare X-linked genetic disease, manifested
as heart disease, intellectual impairment, and developmental disorders. We report a male …
as heart disease, intellectual impairment, and developmental disorders. We report a male …
A novel NONO nonsense variant in a fetus with renal abnormalities
L Rodriguez‐Revenga, A Nadal, V Borobio… - Prenatal …, 2024 - Wiley Online Library
Abstract At 16+ 6‐weeks a fetal scan performed in the second pregnancy of a 42 yo woman
identified a right multicystic dysplastic kidney, left renal agenesis, absent urinary bladder …
identified a right multicystic dysplastic kidney, left renal agenesis, absent urinary bladder …
RNA binding proteins in cardiovascular development and disease.
SK Verma, MN Kuyumcu-Martinez - Current Topics in …, 2024 - europepmc.org
Congenital heart disease (CHD) is the most common birth defect affecting> 1.35 million
newborn babies worldwide. CHD can lead to prenatal, neonatal, postnatal lethality or life …
newborn babies worldwide. CHD can lead to prenatal, neonatal, postnatal lethality or life …
A Novel Mutation of NONO-Associated X-linked Syndromic Intellectual Developmental Disorder-34 in a Fetus
R Huang, S Wu, H Ding, L Wu, H Pi, W Liu, J Liu… - 2024 - researchsquare.com
Background The NONO gene is located on chromosome Xq13. 1 and encodes a nuclear
protein involved in RNA synthesis, transcriptional regulation, and DNA repair. Hemizygous …
protein involved in RNA synthesis, transcriptional regulation, and DNA repair. Hemizygous …
[引用][C] Karin Writzl1, 2*, Blaž Mavčič2, 3, Aleš Maver1, 2, Alenka Hodžić1 and Borut Peterlin1
The NONO-associated X-linked syndromic intellectual developmental disorder-34 (NONO-
XLID) is a rare genetic disorder first described 8years ago (Mircsof et al., 2015). It is caused …
XLID) is a rare genetic disorder first described 8years ago (Mircsof et al., 2015). It is caused …