X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (13) 13
humans (12) 12
female (10) 10
child (8) 8
genetics & heredity (8) 8
male (8) 8
phenotype (6) 6
adolescent (5) 5
adult (5) 5
analysis (5) 5
child, preschool (5) 5
comparative genomic hybridization (5) 5
genes (5) 5
cancer (4) 4
chromosome deletion (4) 4
genetic aspects (4) 4
infant (4) 4
mutation (4) 4
oncology (4) 4
agronomy (3) 3
case-control studies (3) 3
children (3) 3
dna copy number variations (3) 3
gene expression (3) 3
obesity (3) 3
syndrome (3) 3
tomatoes (3) 3
wastewater (3) 3
water resources (3) 3
young adult (3) 3
alleles (2) 2
article (2) 2
association (2) 2
body mass index (2) 2
care and treatment (2) 2
case report (2) 2
cell biology (2) 2
chromosomes, human, pair 16 (2) 2
congenital, hereditary, and neonatal diseases and abnormalities (2) 2
copy number (2) 2
crop yields (2) 2
crops (2) 2
development and progression (2) 2
developmental disabilities - genetics (2) 2
diluted seawater (2) 2
encephalopathy (2) 2
epigenetic deregulation (2) 2
epigenetics (2) 2
escherichia-coli (2) 2
exome (2) 2
fast cell cycle related genes (2) 2
fruits (2) 2
gene (2) 2
gene expression array (2) 2
gene expression profiling (2) 2
gene mutations (2) 2
genetic predisposition to disease (2) 2
genetic research (2) 2
genetics (2) 2
genotype (2) 2
germ-line mutation (2) 2
heterozygote (2) 2
impact (2) 2
inactivation (2) 2
irrigation (2) 2
life sciences (2) 2
management (2) 2
methyl-cpg-binding protein 2 - genetics (2) 2
microsatellite instability (2) 2
middle aged (2) 2
msh6 protein (2) 2
mutations (2) 2
myxoid liposarcoma (2) 2
pedigree (2) 2
phenotypes (2) 2
polymorphism (2) 2
progression to round cell (2) 2
protein expression (2) 2
proteins (2) 2
rb1 gene (2) 2
retinoblastoma - genetics (2) 2
rett syndrome (2) 2
rett syndrome - genetics (2) 2
rett-syndrome (2) 2
reuse (2) 2
risk assessment (2) 2
risk factors (2) 2
risks (2) 2
schizophrenia (2) 2
sequence deletion (2) 2
single nucleotide polymorphisms (2) 2
soil (2) 2
soil science (2) 2
stemness related genes (2) 2
survival (2) 2
testosterone (2) 2
tomato crop (2) 2
tumor (2) 2
waste water (2) 2
x chromosome inactivation (2) 2
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


by Jacquemont, S and Reymond, A and Zufferey, F and Harewood, L and Walters, R.G and Kutalik, Z and Martinet, D and Shen, Y and Valsesia, A and Beckmann, N.D and Thorleifsson, G and Belfiore, M and Bouquillon, S and Campion, D and Leeuw, N. de and Vries, L.B.A. de and Esko, T and Fernandez, B.A and Fernandez-Aranda, F and Fernandez-Real, J.M and Gratacos, M and Guilmatre, A and Hoyer, J and Jarvelin, M.R and Kooy, R.F and Kurg, A and Caignec, C. Le and Mannik, K and Platt, O.S and Sanlaville, D and Haelst, M.M. van and Villatoro Gomez, S and Walha, F and Wu, B.L and Yu, Y and Aboura, A and Addor, M.C and Alembik, Y and Antonarakis, S.E and Arveiler, B and Barth, M and Bednarek, N and Bena, F and Bergmann, S and Beri, M and Bernardini, L and Blaumeiser, B and Bonneau, D and Bottani, A and Boute, O and Brunner, H.G and Cailley, D and Callier, P and Chiesa, J and Chrast, J and Coin, L and Coutton, C and Cuisset, J.M and Cuvellier, J.C and David, A and Freminville, B. de and Delobel, B and Delrue, M.A and Demeer, B and Descamps, D and Didelot, G and Dieterich, K and Disciglio, V and Doco-Fenzy, M and nat, S and Duban-Bedu, B and Dubourg, C and El-Sayed Moustafa, J.S and Elliott, P and Faas, B.H.W and Faivre, L and Faudet, A and Fellmann, F and Ferrarini, A and Fisher, R and Flori, E and Forer, L and Gaillard, D and Gerard, M and Gieger, C and Gimelli, S and Gimelli, G and Grabe, H.J and Guichet, A and Guillin, O and Hartikainen, A.L and Heron, D and Hippolyte, L and Holder, M and Homuth, G and Isidor, B and Jaillard, S and Jaros, Z and Jimenez-Murcia, S and Helas, G.J and ...
Nature, ISSN 0028-0836, 2011, Volume 478, Issue 7367, pp. 97 - 102
Both obesity and being underweight have been associated with increased mortality. Underweight, defined as a body mass index (BMI) DEPENDENT PROBE AMPLIFICATION | FAILURE-TO-THRIVE | METABOLIC SYNDROME | RELATIVE QUANTIFICATION | SNP GENOTYPING DATA | HIDDEN-MARKOV MODEL | MULTIDISCIPLINARY SCIENCES | BODY-MASS INDEX | TIME QUANTITATIVE PCR | COPY NUMBER VARIATION | CIRCULAR BINARY SEGMENTATION | Humans | Middle Aged | Child, Preschool | RNA, Messenger - analysis | Head - anatomy & histology | Infant | Male | Developmental Disabilities - genetics | Gene Expression Profiling | North America | Obesity - genetics | Case-Control Studies | Young Adult | Mental Disorders - genetics | Aging | Gene Duplication - genetics | Adult | Female | Transcription, Genetic | Energy Metabolism - genetics | Child | Infant, Newborn | Chromosomes, Human, Pair 16 - genetics | Body Mass Index | Gene Dosage - genetics | Genetic Predisposition to Disease - genetics | Genome-Wide Association Study | Europe | RNA, Messenger - genetics | Mutation - genetics | Body Height - genetics | Thinness - genetics | Phenotype | Comparative Genomic Hybridization | Adolescent | Heterozygote | Aged | Cohort Studies | Sequence Deletion - genetics | Obesity | Chromosome mapping | Usage | Genetic variation | Genetic aspects | Cognition disorders | Research | Risk factors | Schizophrenia | Gender | Behavior | Gene expression | Bias | Life Sciences | Human health and pathology | Genetics | Endocrinology and metabolism | Gene Duplication | Developmental Disabilities | Sequence Deletion | Thinness | genetics | Genetic Predisposition to Disease | Head | Gene Dosage | analysis | Energy Metabolism | Mental Disorders | Chromosomes, Human, Pair 16 | Body Height | Mutation | anatomy & histology | RNA, Messenger
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 10/2012, Volume 49, Issue 10, pp. 660 - 668
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 07/2014, Volume 164, Issue 7, pp. 1666 - 1676
Journal Article
CELLS, ISSN 2073-4409, 09/2019, Volume 8, Issue 9, p. 1110
Cellular stress response is a universal mechanism that ensures the survival or negative selection of cells in challenging conditions. The transcription factor... 
SKELETAL-MUSCLE ATROPHY | LIFE-SPAN | OXIDATIVE-STRESS | transcription factors | cellular homeostasis | DNA-DAMAGE RESPONSE | HEAT-SHOCK | FORKHEAD PROTEINS | CELL BIOLOGY | KINASE PATHWAYS | nuclear/mitochondrial crosstalk | stress response | GENE-EXPRESSION | FOXO3a | GROWTH-FACTOR | TRANSCRIPTION FACTOR FOXO3A
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 12/2011, Volume 19, Issue 12, pp. 1246 - 1255
Journal Article
International Journal of Biological Markers, ISSN 0393-6155, 2018, Volume 33, Issue 4, pp. 534 - 539
Introduction: Lynch syndrome is caused by germline mutations in one of the mismatch repair genes (MLH1, MSH2, MSH6, and PMS2) or in the EPCAM gene. Lynch... 
Familial cancer | MSH2 | Splicing variant | Lynch syndrome | splicing variant | familial cancer | ONCOLOGY | BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Journal Article
Pathology & Oncology Research, ISSN 1219-4956, 7/2012, Volume 18, Issue 3, pp. 703 - 712
Retinoblastoma is the most common primary intraocular malignancy in children. Two step inactivation of RB1 (M1-M2) represents the key event in the pathogenesis... 
Pathology | Biomedicine | Immunology | MS-MLPA | Epigenetics | Oncology | Cancer Research | Retinoblastoma | Copy number changes | Biomedicine general | MICROSATELLITE INSTABILITY | TUMOR-SUPPRESSOR GENE | P73 GENE | RB1 GENE | PEDIATRIC TUMORS | PATHOLOGY | ABERRANT PROMOTER METHYLATION | DNA MISMATCH REPAIR | ONCOLOGY | COMPARATIVE GENOMIC HYBRIDIZATION | O-6-METHYLGUANINE-DNA METHYLTRANSFERASE | TRANSGENIC MICE | Multiplex Polymerase Chain Reaction - methods | Retina - metabolism | Epigenomics | Prognosis | Retinoblastoma - genetics | Humans | Middle Aged | Child, Preschool | Infant | Male | Promoter Regions, Genetic - genetics | Case-Control Studies | DNA Copy Number Variations | Young Adult | DNA Methylation | Tumor Suppressor Proteins - genetics | Adolescent | Adult | Female | Neoplasm Staging | Child | Anopheles | Neurosciences | Proteolysis | Genes | Medical genetics | Genetic research | Development and progression | Genetic transcription | Tumor proteins | Methylation | Tumors | Transcription | Gene regulation | Data processing | Retina | Malignancy | Cell interactions | Pax5 protein | DNA repair | epigenetics | p53 protein | O6-methylguanine-DNA methyltransferase | MSH6 protein | Signal transduction | CD44 antigen | Glutathione transferase | retinoblastoma | DNA methylation | Tumorigenesis | VHL protein | Children | copy number | Probes | Cell migration
Journal Article
Chinese journal of cancer, ISSN 1000-467X, 06/2016, Volume 35, Issue 1, pp. 51 - 14
Journal Article