Results 51 to 60 of about 63,165 (118)
Signaling through the mechanistic target of rapamycin complex 1 (mTORC1) is a major regulatory node of pro‐inflammatory mediator production by macrophages (MΦs).
M. William +5 more
semanticscholar +1 more source
The dynamic mechanism of 4E-BP1 recognition and phosphorylation by mTORC1.
R. Böhm +5 more
semanticscholar +1 more source
The 15q11.2 BP1–BP2 microdeletion (Burnside–Butler) syndrome is an emerging disorder that encompasses four genes (NIPA1, NIPA2, CYFIP1, and TUBGCP5).
M. Butler
semanticscholar +1 more source
Rotavirus infection is a major cause of severe dehydrating diarrhea in infants younger than 5 y old and in particular cases of immunocompromised patients irrespective to the age of the patients. Although vaccines have been developed, antiviral therapy is
Yuebang Yin +11 more
semanticscholar +1 more source
Objective: Major depression (MDD) and a lifetime history of MDD are characterized by increased nitrosylation, while bipolar disorder type 1 (BP1), but not BP2, is accompanied by highly increased levels of oxidative stress and nitric oxide (NO) production.
M. Maes +3 more
semanticscholar +1 more source
The consequences of increased 4E-BP1 in polycystic kidney disease.
Autosomal Dominant Polycystic kidney disease (ADPKD) is the most common hereditary renal disease, characterized by cyst formation and growth. Hyperproliferation is a major contributor to cyst growth.
S. Holditch +11 more
semanticscholar +1 more source
The 15q11.2 BP1–BP2 Microdeletion Syndrome: A Review
Patients with the 15q11.2 BP1–BP2 microdeletion can present with developmental and language delay, neurobehavioral disturbances and psychiatric problems. Autism, seizures, schizophrenia and mild dysmorphic features are less commonly seen. The 15q11.2 BP1–
Devin M Cox, M. Butler
semanticscholar +1 more source
Expression of 4E-BP1 in juvenile mice alleviates mTOR-induced neuronal dysfunction and epilepsy.
Lena H. Nguyen +7 more
semanticscholar +1 more source

