Results 91 to 100 of about 13,403 (131)

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

Targeting the Notch Signaling Pathway to Treat Atherosclerosis. [PDF]

Cells
Blagov A, Borodko D, Rozhkova U, Antonov S, Utkina A, Kovyanova T.   +5 more
europepmc   +1 more source

NICD3 mediates pro-angiogenic effects through SMAD3/TGFBI axis in colorectal cancer. [PDF]

Cell Death Dis
An R, Yu R, Wen X, Ma Q, Mao K, Zhang Q, Mao L, Feng X, Xin F, Liu P, Wang Y, Zhang J, Huang H, Yan X, Wang W.   +14 more
europepmc   +1 more source

Age-dependent vascular and neurological characteristics of CADASIL are recapitulated in Notch3 mutant zebrafish, implicating a role for type IV collagen in disease progression. [PDF]

Acta Neuropathol Commun
Kanoh T, Oubayashi S, Furukawa K, Fujimoto K, Inoue A, Mizoguchi T, Yamaguchi M, Takahashi-Nakaguchi A, Hasegawa Y, Ohara O, Aoki I, Itoh M.   +11 more
europepmc   +1 more source

Camrelizumab plus nimotuzumab as second-line therapy for advanced esophageal squamous cell carcinoma: a multicenter phase II study. [PDF]

J Immunother Cancer
Xia J, Meng X, Jiang G, Hong Y, Ji Y, Wang C, Yang X, Meng Y, Zhang W, Luo Z, Cui D, Wang J, Shan Z, Guan L, Lu Y, Yang X, Ren C, Meng X, Wang H, Shen L, Zhang Y, Kou Z, Lu T, Fan Q, Quante M, Zhao T, Li S, Wang F.   +27 more
europepmc   +1 more source

Pan-cancer analysis of Notch pathway-linked gene expression identifies tumour-specific and sex-stratified prognostic associations. [PDF]

Clin Transl Radiat Oncol
O'Hea H, Bourbonne V, Marignol L.
europepmc   +1 more source

NOTCH3 gene polymorphism is associated with the prognosis of gliomas in Chinese patients. [PDF]

Medicine (Baltimore), 2015
Shen Z, Hou X, Chen B, Chen P, Zhang Q.
europepmc   +1 more source

Prenatal Etiology Diagnosis of Rare Compound Heterozygous PROC Gene Variants in a Fetus With Ocular Ultrasonic Anomaly Using Whole Exome Sequencing. [PDF]

Mol Genet Genomic Med
Zhuang J, Huang N, Gu L, Fu W.
europepmc   +1 more source

Shared molecular features and candidate pathways underlying gastric cancer-depression comorbidity: a systems biology analysis. [PDF]

Front Bioinform
Liu B, Hou B, Zhao Y, Niu J, Hou J, He J, Liu F.   +6 more
europepmc   +1 more source