Works matching IS 09646906 AND DT 2023 AND VI 32 AND IP 20

Results: 8

Predicted leukocyte telomere length and risk of myeloid neoplasms.
Published in:
Human Molecular Genetics, 2023, v. 32, n. 20, p. 2996, doi. 10.1093/hmg/ddad126
By:
- Sullivan, Shannon M;
- Cole, Ben;
- Lane, John;
- Meredith, John J;
- Langer, Erica;
- Hooten, Anthony J;
- Roesler, Michelle;
- McGraw, Kathy L;
- Pankratz, Nathan;
- Poynter, Jenny N
Publication type:
Article
Correction to: ''Hippocampal mutant APP and amyloid beta-induced cognitive decline, dendritic spine loss, defective autophagy, mitophagy and mitochondrial abnormalities in a mouse model of Alzheimer's disease''.
Published in:
Human Molecular Genetics, 2023, v. 32, n. 20, p. 3027, doi. 10.1093/hmg/ddad147
Publication type:
Article
Correction to: The potential of utrophin and dystrophin combination therapies for Duchenne muscular dystrophy.
Published in:
Human Molecular Genetics, 2023, v. 32, n. 20, p. 3026, doi. 10.1093/hmg/ddad145
Publication type:
Article
Arginine methylation of RNA-binding proteins is impaired in Huntington's disease.
Published in:
Human Molecular Genetics, 2023, v. 32, n. 20, p. 3006, doi. 10.1093/hmg/ddad125
By:
- Ratovitski, Tamara;
- Kamath, Siddhi V;
- O'Meally, Robert N;
- Gosala, Keerthana;
- Holland, Chloe D;
- Jiang, Mali;
- Cole, Robert N;
- Ross, Christopher A
Publication type:
Article
Hemizygous variants in protein phosphatase 1 regulatory subunit 3F (PPP1R3F) are associated with a neurodevelopmental disorder characterized by developmental delay, intellectual disability and autistic features.
Published in:
Human Molecular Genetics, 2023, v. 32, n. 20, p. 2981, doi. 10.1093/hmg/ddad124
By:
- Liu, Zhigang;
- Xin, Baozhong;
- Smith, Iris N;
- Sency, Valerie;
- Szekely, Julia;
- Alkelai, Anna;
- Shuldiner, Alan;
- Efthymiou, Stephanie;
- Rajabi, Farrah;
- Coury, Stephanie;
- Brownstein, Catherine A;
- Rudnik-Schöneborn, Sabine;
- Bruel, Ange-Line;
- Thevenon, Julien;
- Zeidler, Shimriet;
- Jayakar, Parul;
- Schmidt, Axel;
- Cremer, Kirsten;
- Engels, Hartmut;
- Peters, Sophia O
Publication type:
Article
Human herpesvirus 8 ORF57 protein is able to reduce TDP-43 pathology: network analysis identifies interacting pathways.
Published in:
Human Molecular Genetics, 2023, v. 32, n. 20, p. 2966, doi. 10.1093/hmg/ddad122
By:
- Webber, Chelsea J;
- Murphy, Caroline N;
- Rondón-Ortiz, Alejandro N;
- Spek, Sophie J F van der;
- Kelly, Elena X;
- Lampl, Noah M;
- Chiesa, Giulio;
- Khalil, Ahmad S;
- Emili, Andrew;
- Wolozin, Benjamin
Publication type:
Article
AAV9-mediated SMN gene therapy rescues cardiac desmin but not lamin A/C and elastin dysregulation in Smn<sup>2B/−</sup> spinal muscular atrophy mice.
Published in:
Human Molecular Genetics, 2023, v. 32, n. 20, p. 2950, doi. 10.1093/hmg/ddad121
By:
- Brown, Sharon J;
- Šoltić, Darija;
- Synowsky, Silvia A;
- Shirran, Sally L;
- Chilcott, Ellie;
- Shorrock, Hannah K;
- Gillingwater, Thomas H;
- Yáñez-Muñoz, Rafael J;
- Schneider, Bernard;
- Bowerman, Melissa;
- Fuller, Heidi R
Publication type:
Article
Mapping microRNA expression quantitative trait loci in the prenatal human brain implicates miR-1908-5p expression in bipolar disorder and other brain-related traits.
Published in:
Human Molecular Genetics, 2023, v. 32, n. 20, p. 2941, doi. 10.1093/hmg/ddad118
By:
- Toste, Carolina C;
- O'Donovan, Michael C;
- Bray, Nicholas J
Publication type:
Article