Results 271 to 280 of about 91,885 (305)

Classic Hairy Cell Leukemia With MAP2K1 Mutation: Diagnosis and Targeted Therapy

open access: yes
American Journal of Hematology, Volume 101, Issue 2, Page 339-340, February 2026.
Andrea Duminuco   +5 more
wiley   +1 more source

Gonadal function in males with WFS1 spectrum disorder (Wolfram syndrome)—A European cohort perspective

open access: yesAndrology, Volume 14, Issue 2, Page 398-410, February 2026.
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]

open access: yesVavilovskii Zhurnal Genet Selektsii
Yushkova AA   +5 more
europepmc   +1 more source

The Calcium‐Binding Protein S100A10 (p11) Is Required for Normal Motor Performance by Regulating Vesicle Dynamics at Excitatory Synapses

open access: yesActa Physiologica, Volume 242, Issue 2, February 2026.
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

Positive coactivator PC4 shows dynamic nucleolar distribution required for rDNA transcription and protein synthesis. [PDF]

open access: yesCell Commun Signal
Kaypee S   +7 more
europepmc   +1 more source

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