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BBA - Reviews on Cancer, ISSN 0304-419X, 12/2019, Volume 1872, Issue 2, p. 188310
Systemic therapy often results in the reduction of tumor size but rarely succeeds in eradicating all cancer cells. Drug efflux, persistence of cancer stem... 
Tumor heterogeneity | Mutation | Drug resistance | Cancer
Journal Article
Current pharmaceutical design, 2017, Volume 23, Issue 32, pp. 4794 - 4806
Journal Article
Journal of Human Genetics, ISSN 1434-5161, 05/2018, Volume 63, Issue 5, pp. 597 - 604
Tuberous sclerosis (TS) is a rare autosomal-dominant genetic disease. TS is manifested by the development of multiple hamartomas, which affect brain, kidneys,... 
COMPLEX | GENOTYPE-PHENOTYPE CORRELATIONS | UNRELATED PATIENTS | GENE | EVEROLIMUS | FREQUENCY | GENETICS & HEREDITY | KOREAN PATIENTS | JAPANESE PATIENTS | IDENTIFICATION | SEVERITY
Journal Article
Investigational new drugs, ISSN 0167-6997, 08/2019, pp. 1 - 5
Colorectal carcinomas (CRCs) caused by hereditary biallelic MUTYH gene mutations are characterized by elevated mutation load and high lymphocyte infiltration.... 
Microsatellites | Stability | Invasiveness | Colorectal carcinoma | Colorectal cancer | Microsatellite instability | Metastases | Chemotherapy | Immune checkpoint | Lymphocytes | Infiltration | Mutation | Tumors | Cancer
Journal Article
European journal of medical genetics, ISSN 1769-7212, 09/2019, p. 103753
Hereditary non-polyposis colorectal cancer (HNPCC), also known as Lynch syndrome (LS), is a common cancer-predisposing syndrome. This study aimed to... 
Journal Article
Biochimie, ISSN 0300-9084, 11/2018, Volume 154, pp. 19 - 24
Journal Article
Journal Article
Cureus, ISSN 2168-8184, 02/2018, Volume 10, Issue 2
This report describes an estrogen receptor-positive breast cancer patient, who relapsed at two and a half years after the completion of adjuvant chemotherapy... 
Chemotherapy | Liver | Clinical trials | Cytotoxicity | Breast cancer | Metastasis | Mutation | Patients | Cancer therapies | Drug dosages | Deoxyribonucleic acid--DNA | Tumors
Journal Article
Cancer Research, ISSN 0008-5472, 07/2016, Volume 76, Issue 14 Supplement, pp. 2928 - 2928
Approximately 15-25 ovarian cancer (OC) patients carry germ-line mutation in BRCA1 or BRCA2 genes. BRCA deficiency underlies the pronounced sensitivity of... 
Journal Article
Cancer Cytopathology, ISSN 1934-662X, 07/2013, Volume 121, Issue 7, pp. 370 - 376
Journal Article
Molecular Syndromology, ISSN 1661-8769, 05/2016, Volume 7, Issue 2, pp. 62 - 71
Bardet-Biedl syndrome (BBS) is a rare autosomal recessive genetic disorder. It is characterized by heterogeneous clinical manifestations including primary... 
Review Article | Ciliopathy | Bardet-Biedl syndrome | Treatment | Review | Recurrent mutations | Ethnic variations
Journal Article
Case Reports in Oncology, ISSN 1662-6575, 01/2019, Volume 12, Issue 1, pp. 109 - 112
Approximately 15% of acral and mucous melanomas carry activating mutations in KIT oncogene. There is a diversity of spectrum of KIT mutations, with some of... 
Case Report | Imatinib | Mutation | Melanoma | KIT
Journal Article
Cancer Research, ISSN 0008-5472, 04/2012, Volume 72, Issue 8 Supplement, pp. 2597 - 2597
Journal Article
Translational Cancer Research, ISSN 2218-676X, 08/2017, Volume 6, Issue S6, pp. S995 - S998
Journal Article