Results 271 to 280 of about 91,885 (305)
Classic Hairy Cell Leukemia With MAP2K1 Mutation: Diagnosis and Targeted Therapy
American Journal of Hematology, Volume 101, Issue 2, Page 339-340, February 2026.
Andrea Duminuco +5 more
wiley +1 more source
Abstract Background WFS1 spectrum disorder, also known as Wolfram syndrome (WS) is an ultra‐rare (<1:500,000; ORPHA: 3463) monogenic (OMIM #222300) progressive neuroendocrine and neurodegenerative disorder, characterised by early‐onset insulin‐dependent diabetes, optic atrophy, central diabetes insipidus and sensi‐neuronal deafness.
Julia Rohayem +6 more
wiley +1 more source
The effects of Non3 mutations on chromatin organization in Drosophila melanogaster. [PDF]
Yushkova AA +5 more
europepmc +1 more source
ABSTRACT Aim Identifying interactors in sensorimotor processing and neurotransmission remains a current challenge for understanding neural information processing and brain function. Methods To evaluate the role of p11 in sensorimotor processing and excitatory synaptic neurotransmission, neuron‐specific lentivirus‐directed p11 silencing, small ...
Esther Vilches‐Herrando +7 more
wiley +1 more source
AML Disparities Across Racial Ancestry Groups: A Spotlight on the NPM1 Mutations. [PDF]
Sanaullah SA, Vidi PA, Pardee TS.
europepmc +1 more source
Correction: Nuclei Segmentation and Classification from Histopathology Images using Federated Learning for End-Edge Platform. [PDF]
PLOS One Staff.
europepmc +1 more source
The nucleolus of a matrix game and other nucleoli
J.A.M. Potters, S.H. Tijs
openalex +1 more source
Positive coactivator PC4 shows dynamic nucleolar distribution required for rDNA transcription and protein synthesis. [PDF]
Kaypee S +7 more
europepmc +1 more source
The science and legacies of Ronald Phillips: A brief perspective. [PDF]
Flavell RB.
europepmc +1 more source

