The ankyrin repeat as molecular architecture for protein recognition
LK Mosavi, TJ Cammett, DC Desrosiers… - Protein science, 2004 - Wiley Online Library
The ankyrin repeat is one of the most frequently observed amino acid motifs in protein
databases. This protein–protein interaction module is involved in a diverse set of cellular …
databases. This protein–protein interaction module is involved in a diverse set of cellular …
Regulatory Mechanisms of Tumor Suppressor P16INK4A and Their Relevance to Cancer
J Li, MJ Poi, MD Tsai - Biochemistry, 2011 - ACS Publications
P16INK4A (also known as P16 and MTS1), a protein consisting exclusively of four ankyrin
repeats, is recognized as a tumor suppressor mainly because of the prevalence of genetic …
repeats, is recognized as a tumor suppressor mainly because of the prevalence of genetic …
[HTML][HTML] Vemurafenib induces senescence features in melanoma cells
S Haferkamp, A Borst, C Adam, TM Becker… - Journal of Investigative …, 2013 - Elsevier
A large proportion of human melanomas harbor a mutation leading to permanent activation
of the serine/threonine kinase BRAF, and as a consequence, they have developed …
of the serine/threonine kinase BRAF, and as a consequence, they have developed …
The p16INK4A tumor suppressor regulates cellular oxidative stress
NC Jenkins, T Liu, P Cassidy, SA Leachman… - Oncogene, 2011 - nature.com
Mutations or deletions in the cyclin-dependent kinase inhibitor p16 INK4A are associated
with multiple cancer types, but are more commonly found in melanoma tumors and …
with multiple cancer types, but are more commonly found in melanoma tumors and …
Interpreting missense variants: comparing computational methods in human disease genes CDKN2A, MLH1, MSH2, MECP2, and tyrosinase (TYR)
PA Chan, S Duraisamy, PJ Miller, JA Newell… - Human …, 2007 - Wiley Online Library
The human genome contains frequent single‐basepair variants that may or may not cause
genetic disease. To characterize benign vs. pathogenic missense variants, numerous …
genetic disease. To characterize benign vs. pathogenic missense variants, numerous …
Assessment of functional effects of unclassified genetic variants
FJ Couch, LJ Rasmussen, R Hofstra… - Human …, 2008 - Wiley Online Library
Inherited predisposition to disease is often linked to reduced activity of a disease associated
gene product. Thus, quantitation of the influence of inherited variants on gene function can …
gene product. Thus, quantitation of the influence of inherited variants on gene function can …
Evaluation of Bioactive Properties of Lipophilic Fractions of Edible and Non-Edible Parts of Nasturtium officinale (Watercress) in a Model of Human Malignant …
Watercress is an enriched source of phenethyl isothiocyanate (PEITC), among other
phytochemicals, with an antioxidant capacity. The aim of this study was to (i) chemically …
phytochemicals, with an antioxidant capacity. The aim of this study was to (i) chemically …
[HTML][HTML] Blood-based DNA methylation biomarkers for early detection of colorectal cancer
L Dong, H Ren - Journal of proteomics & bioinformatics, 2018 - ncbi.nlm.nih.gov
Colorectal cancer (CRC) is a leading cause of cancer-related deaths worldwide. Early
detection of CRC can significantly reduce this mortality rate. Unfortunately, recommended …
detection of CRC can significantly reduce this mortality rate. Unfortunately, recommended …
Genetic alterations in the INK4a/ARF locus: effects on melanoma development and progression
Genetic alterations in the INK4a/ARF (or CDKN2A) locus have been reported in many
cancer types, including melanoma; head and neck squamous cell carcinomas; lung, breast …
cancer types, including melanoma; head and neck squamous cell carcinomas; lung, breast …
CDKN2A Gene Mutations: Implications for Hereditary Cancer Syndromes
A Danishevich, A Bilyalov, S Nikolaev, N Khalikov… - Biomedicines, 2023 - mdpi.com
Malignant neoplasms, including pancreatic cancer and melanoma, are major global health
challenges. This study investigates melanoma pancreatic syndrome, a rare hereditary tumor …
challenges. This study investigates melanoma pancreatic syndrome, a rare hereditary tumor …