Results 131 to 140 of about 2,529,587 (194)

LncRNA <i>RAMS11</i>-dependent <i>NOTCH3</i> activation drives tumor progression in non-small cell lung cancer. [PDF]

NAR Cancer
Jeffers GG, Kim Y, White NM, Lin L, Rozycki EB, Ly A, Maher CA.   +6 more
europepmc   +1 more source

NOTCH3 disrupts the osteoblast transcriptome in femoral bone of 1-month-old male C57BL/6 mice. [PDF]

Bone
Canalis E, Schilling L, Denker E.
europepmc   +1 more source

Impairment of hippocampal gamma oscillations, mitochondria and neurovascular function in CADASIL. [PDF]

Brain
Shao W, Oliveira DV, Naia L, Li Y, Bjørnholm KD, Isla AG, Uhlén P, Kalaria R, Lesnik Oberstein SAJ, Lendahl U, Enrique Arroyo-García L, Jin S, Karlström H.   +12 more
europepmc   +1 more source

Small molecule-mediated activation of Notch signal transduction. [PDF]

Cell Death Dis
Dey S, Giaimo BD, Zöllner IK, Yang Q, Zarrin H, Ballout J, Diener M, Friedrich T, Ferrante F, Dreute J, Schmitz ML, Weiss A, Polo P, Lauth M, Gahr B, Just S, Bartkuhn M, Oswald F, Borggrefe T.   +18 more
europepmc   +1 more source

Loss-of-function Mutation in the NOTCH3 Gene: Simply a Polymorphism? [PDF]

Human Mutation, 2013
openaire   +2 more sources

Notch3/4 Knockdown Inhibits Colon Adenocarcinoma Progression by Suppressing Tumor Cell Activity and Orchestrating VEGFA-Dependent Tumor Immune Microenvironment. [PDF]

Cancer Med
Liu W, Tang G, Li N, Wang J, Zhao H, Li C.   +5 more
europepmc   +1 more source

NOTCH3 regulates myofibroblastic CAF differentiation via the P62-ROS signaling axis to promote bladder cancer progression. [PDF]

J Exp Clin Cancer Res
Hu D, Shen C, Liu C, Xie F, Wang X, Wang H, Chen Y, Zhao X, Qin R, Li C, Ge H, Zhu J, Xi Z, Wang Y.   +13 more
europepmc   +1 more source

The Association Between the Genetic Variants of the NOTCH3 Gene and Ischemic Stroke Risk. [PDF]

Med Sci Monit, 2016
Yuan X, Dong Z.
europepmc   +1 more source

A novel missense variant Cys559Gly in <i>NOTCH3</i> in CADASIL family and vascular lesions in patients with migraine. [PDF]

Postep Psychiatr Neurol
Jastrzębski K, Kępczyński Ł, Plucińska A, Kowalska-Gałecka M, Gajos A.   +4 more
europepmc   +1 more source

A Clinical Genetics-Driven Dual Diagnosis of Prader-Willi Syndrome Due to Mosaic Maternal UPD(15) and <i>NOTCH3</i>-Related CADASIL. [PDF]

Genes (Basel)
Bogliardi FM, D'Ambrosio P, Quattromini G, Di Mario G, Pomponi MG, Miele L, Vergani E, Zampino G, Liguori A, Zollino M, Crinò A.   +10 more
europepmc   +1 more source