Results 221 to 230 of about 946,920 (339)
Dynamic Gene Regulatory Networks of Human Myeloid Differentiation.
Ricardo N. Ramirez +5 more
semanticscholar +1 more source
ABSTRACT Objective Super‐Refractory Status Epilepticus (SRSE) is a rare, life‐threatening neurological emergency with unclear etiology in many cases. Mitochondrial dysfunction, often due to disease‐causing genetic variants, is increasingly recognized as a cause, with each gene producing distinct pathophysiological mechanisms.
Pouria Mohammadi +2 more
wiley +1 more source
SC-MO-GRN-DB: A comprehensive repository for single-cell multiomic gene regulatory networks. [PDF]
Valensi H +5 more
europepmc +1 more source
Epigenetic reprogramming in hematopoietic stem and progenitor cells (HSPCs) and downstream myeloid cells, mediated by H3.3 downregulation and endogenous retroelement (ERE) overexpression, contributes to the progression of multiple sclerosis (MS). ABSTRACT Background Skewed myelopoiesis in the bone marrow has been identified as a key driver of multiple ...
Li‐Mei Xiao +6 more
wiley +1 more source
Dissecting gene regulatory networks governing human cortical cell fate. [PDF]
Ding JW +8 more
europepmc +1 more source
Computational inference of gene regulatory networks: Approaches, limitations and opportunities.
M. Banf, S. Rhee
semanticscholar +1 more source
A Depolarizing Leak in Sodium Bicarbonate Cotransporter NBCe1 Causes Brain Edema
ABSTRACT Objectives SLC4A4 encodes electrogenic sodium bicarbonate cotransporter NBCe1, prominently expressed in kidney and brain. Recessive loss‐of‐function variants in SLC4A4 cause proximal renal tubular acidosis, no brain edema. In the brain, NBCe1 is expressed by astrocytes, where it regulates pH and mediates astrocyte volume changes.
Quinty Bisseling +16 more
wiley +1 more source
Big data approaches to understanding gene regulatory networks in the shoot apical meristem and <i>de novo</i> shoot regeneration. [PDF]
Carpenter JH +3 more
europepmc +1 more source
SPG4 and Dementia: Expanding the Clinical Spectrum
ABSTRACT Objective Hereditary spastic paraplegia (HSP) is a group of disorders characterized by progressive spasticity and lower limb weakness, with mutations in SPG4/SPAST being the most common cause. Detailed studies and clinical and molecular comparisons across different populations are missing.
Emanuele Panza +19 more
wiley +1 more source
RegNetwork 2025: an integrative data repository for gene regulatory networks in human and mouse. [PDF]
Li B, Wang C, Wang Y, Li P, Liu ZP.
europepmc +1 more source

