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Molecular portraits of cell cycle checkpoint kinases in cancer evolution, progression, and treatment responsiveness | Science Advances
Genes | Free Full-Text | Clinicopathologic Profile of Breast Cancer in Germline ATM and CHEK2 Mutation Carriers
Homozygosity for CHEK2 p.Gly167Arg leads to a unique cancer syndrome with multiple complex chromosomal translocations in peripheral blood karyotype | Journal of Medical Genetics
Genetic Disorder Reference Sheet: CHEK2 Gene Pathogenic Variants
A novel recurrent CHEK2 Y390C mutation identified in high-risk Chinese breast cancer patients impairs its activity and is associated with increased breast cancer risk | Oncogene
The CHEK2 gene and its putative association with human ageing
Skin cancer risk in CHEK2 mutation carriers - Bui - 2021 - Journal of the European Academy of Dermatology and Venereology - Wiley Online Library
Novel and Loss of Function CHEK2 Mutation Underlies Early Onset Breast Cancer in China----Chinese Academy of Sciences
ICARE Social Media Post July 2020Breast Cancer Risks May be Higher in Women with Two CHEK2 Mutations Versus One CHEK2 Mutation – Inherited Cancer Registry (ICARE)
a ) Structure of human CHEK2 gene. The CHEK2 gene localizes to... | Download Scientific Diagram
CHEK2 - Wikipedia
CHEK2 Gene Mutations Increase Breast Cancer Risk - CancerConnect
CHEK2 variants: linking functional impact to cancer risk: Trends in Cancer
CHEK2: Cancer Genetic Test
JCI Insight - Germline mutations in a DNA repair pathway are associated with familial colorectal cancer
Breasts at risk: researchers decipher hundreds of variants of breast cancer gene - Akademie věd České republiky
CHeK2 pathway. CHeK2 is activated upon DNA damage. it is phosphorylated... | Download Scientific Diagram
Cancer risk and CHEK2 gene mutations
Impact of germline and somatic cell cycle checkpoint kinase mutations on breast cancer presentation and prognosis | bioRxiv
ICARE Social Media Post March 2020Study Based on ICARE Participants with ATM and CHEK2 Mutations – Inherited Cancer Registry (ICARE)
A risk of essential thrombocythemia in carriers of constitutional CHEK2 gene mutations | Haematologica
Moderate penetrance genes complicate genetic testing for breast cancer diagnosis: ATM, CHEK2, BARD1 and RAD51D - The Breast
Association of Germline CHEK2 Gene Variants with Risk and Prognosis of Non-Hodgkin Lymphoma | PLOS ONE
CHEK2 Carrier Modification with Polygenic Risk Score | Myriad Oncology
Gene Mutation CHEK2 and Cancer Risk
CHEK2 contribution to hereditary breast cancer in non-BRCAfamilies | Breast Cancer Research | Full Text
