X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (130) 130
index medicus (103) 103
female (78) 78
mutation (67) 67
oncology (56) 56
middle aged (53) 53
genetics & heredity (49) 49
adult (48) 48
male (46) 46
cancer (43) 43
genes (37) 37
genetic aspects (37) 37
colorectal cancer (35) 35
tumors (33) 33
aged (32) 32
colorectal neoplasms - genetics (32) 32
breast cancer (31) 31
genetics (31) 31
pathology (30) 30
genetic predisposition to disease (29) 29
risk (28) 28
risk factors (28) 28
germ-line mutation (24) 24
microsatellite instability (24) 24
research (24) 24
breast neoplasms - genetics (23) 23
heterozygote (23) 23
gene mutations (22) 22
gene (19) 19
medicin och hälsovetenskap (19) 19
mutations (19) 19
medical and health sciences (18) 18
medicine (18) 18
pedigree (18) 18
alleles (17) 17
base sequence (17) 17
deoxyribonucleic acid--dna (17) 17
netherlands (17) 17
colorectal neoplasms, hereditary nonpolyposis - genetics (16) 16
dna mutational analysis (16) 16
genes, brca1 (16) 16
genes, brca2 (16) 16
immunohistochemistry (16) 16
analysis (15) 15
biochemistry & molecular biology (15) 15
cancer och onkologi (15) 15
carcinoma (15) 15
expression (15) 15
lynch syndrome (15) 15
molecular sequence data (15) 15
young adult (15) 15
cell biology (14) 14
colorectal-cancer (14) 14
genotype (14) 14
health aspects (14) 14
adolescent (13) 13
article (13) 13
brca1 protein - genetics (13) 13
cancer and oncology (13) 13
genetic variation (13) 13
muts homolog 2 protein - genetics (13) 13
nonpolyposis colorectal-cancer (13) 13
skin and connective tissue diseases (13) 13
brca2 protein - genetics (12) 12
diagnosis (12) 12
genetic research (12) 12
genetic testing (12) 12
neoplasms - genetics (12) 12
ovarian cancer (12) 12
brca1 protein (11) 11
breast (11) 11
care and treatment (11) 11
clinical medicine (11) 11
cohort studies (11) 11
digestive system diseases (11) 11
epidemiology (11) 11
families (11) 11
germline mutations (11) 11
klinisk medicin (11) 11
medical research (11) 11
methylation (11) 11
polymorphism, single nucleotide (11) 11
reproducibility of results (11) 11
biomarkers, tumor - genetics (10) 10
brca2 protein (10) 10
cancer research (10) 10
dna methylation (10) 10
dna mutational analysis - methods (10) 10
dna sequencing (10) 10
genetic testing - methods (10) 10
identification (10) 10
medicine & public health (10) 10
metastasis (10) 10
mutation - genetics (10) 10
prognosis (10) 10
proteins (10) 10
research article (10) 10
stomach neoplasms - genetics (10) 10
age (9) 9
biomedicine (9) 9
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Scientific reports, ISSN 2045-2322, 06/2019, Volume 9, Issue 1, pp. 8239 - 13
Mutations in the RAS genes are identified in a variety of clinical settings, ranging from somatic mutations in oncology to germline mutations in developmental... 
Amino acids | GTP | Mutation | Guanine nucleotide exchange factor | Guanine | K-Ras protein
Journal Article
Journal of the National Cancer Institute, ISSN 0027-8874, 07/2019
Journal Article
Cancer Biology & Therapy, ISSN 1538-4047, 07/2019, Volume 20, Issue 7, pp. 949 - 955
Acinar cell carcinoma (ACC) is a rare pancreatic neoplasm with dismal prognosis. Insights into the molecular basis of ACC can pave the way for the application... 
Acinar cell carcinoma of the pancreas | BRCA1 | somatic mutation | BRCA2 | germline mutation | SURVIVAL | NEOPLASMS | ONCOLOGY | ADENOCARCINOMA | CANCER
Journal Article
BRITISH JOURNAL OF CANCER, ISSN 0007-0920, 07/2019, Volume 121, Issue 1, pp. 34 - 36
Advances in molecular tumour diagnostics and the number of targeted therapies increase rapidly. Molecular tumour boards (MTBs) are designated to interpret... 
UNIVERSITY-OF-CALIFORNIA | IMPACT | ONCOLOGY | MEDICINE | Medical research | Cost assessments | Diagnostic tests | Quality control | Clinical trials | Oncology | Knowledge management | Medical diagnosis | Patients | Tumors | Cancer
Journal Article
Virchows Archiv, ISSN 0945-6317, 2019, Volume 474, Issue 6, pp. 673 - 680
Journal Article
Nederlands tijdschrift voor geneeskunde, ISSN 0028-2162, 05/2019, Volume 163
Genetic testing in patients with cancer; new developments About 5% of patients with cancer have a causative germline mutation. When a germline mutation is... 
Journal Article
Nederlands tijdschrift voor geneeskunde, 05/2019, Volume 163
Journal Article
Journal of the National Cancer Institute, ISSN 0027-8874, 05/2019
Women with epithelial ovarian cancer (OC) have a higher chance to benefit from PARP inhibitor (PARPi) therapy if their tumor has a somatic or hereditary... 
Journal Article
Familial Cancer, ISSN 1389-9600, 4/2019, Volume 18, Issue 2, pp. 281 - 284
Journal Article
Cancer Cell, ISSN 1535-6108, 02/2019, Volume 35, Issue 2, pp. 256 - 266.e5
Biallelic germline mutations affecting predispose carriers to adenomatous polyposis and colorectal cancer, but the complete phenotype is unknown. We describe... 
adenomatous polyposis | colorectal cancer | somatic mutation spectrum | NTHL1 | base excision repair | genetic predisposition | DNA repair defect | breast cancer | multiple malignancies | mutational signature | ONCOLOGY | POLYPOSIS | GERMLINE MUTATIONS | RISK | LYNCH SYNDROME | SPECTRUM | CANCER | MUTYH | CELL BIOLOGY | Analysis | Genetic aspects | Tumors
Journal Article
Journal Article
Human Mutation, ISSN 1059-7794, 03/2018, Volume 39, Issue 3, pp. 394 - 405
Journal Article