Results 241 to 250 of about 7,770,494 (359)
Neonatal hypophosphatasia: a case report of a rare genetic disorder. [PDF]
Vohra WI, Chohan N, Mirza A.
europepmc +1 more source
Genetic variation in IL28B predicts hepatitis C treatment-induced viral clearance
D. Ge +12 more
semanticscholar +1 more source
Detection of extrachromosomal circular DNA (eccDNA) in plasma samples from EGFR‐mutated non‐small cell lung cancer patients. Plasma was collected before and during treatment with the EGFR‐tyrosine kinase inhibitor osimertinib. Plasma eccDNA was detected in all cancer samples, and the presence of the EGFR gene on eccDNA serves as a potential biomarker ...
Simone Stensgaard +5 more
wiley +1 more source
Antibody-Positive Type 1 Diabetes in a Family With a Pathogenic <i>HNF1A</i>-MODY Variant and Variable Age of Onset. [PDF]
McCullough ME +5 more
europepmc +1 more source
Survivin and Aurora Kinase A control cell fate decisions during mitosis
Aurora A interacts with survivin during mitosis and regulates its centromeric role. Loss of Aurora A activity mislocalises survivin, the CPC and BubR1, leading to disruption of the spindle checkpoint and triggering premature mitotic exit, which we refer to as ‘mitotic slippage’.
Hana Abdelkabir +2 more
wiley +1 more source
Vunakizumab for Treatment of Acrodermatitis Continua of Hallopeau: A Case Report and Literature Review. [PDF]
Yao Y +6 more
europepmc +1 more source
A mouse model for vascular normalization and a human breast cancer cohort were studied to understand the relationship between vascular leakage and tumor immune suppression. For this, endothelial and immune cell RNAseq, staining for vascular function, and immune cell profiling were employed.
Liqun He +8 more
wiley +1 more source
Diabetes mellitus <i>HNF4A</i>-MODY in children from the Russian population: clinical and genetic features. [PDF]
Sechko EA +9 more
europepmc +1 more source

