X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (121) 121
humans (105) 105
genetics & heredity (56) 56
female (51) 51
male (41) 41
animals (35) 35
molecular sequence data (33) 33
chromosome mapping (32) 32
mutation (30) 30
article (27) 27
base sequence (27) 27
neoplasm proteins - genetics (26) 26
oncology (24) 24
gene (23) 23
genes (23) 23
multiple endocrine neoplasia type 1 - genetics (23) 23
cancer (21) 21
polymerase chain reaction (21) 21
proto-oncogene proteins (21) 21
adult (20) 20
biochemistry & molecular biology (19) 19
mice (19) 19
genetic markers (18) 18
genetics (18) 18
mutations (18) 18
research (18) 18
genetic aspects (17) 17
alleles (16) 16
cell biology (16) 16
cloning, molecular (16) 16
pedigree (16) 16
tumors (16) 16
analysis (15) 15
genomics (15) 15
chromosomes, human, pair 17 (14) 14
genetic research (14) 14
middle aged (14) 14
sequence analysis, dna (14) 14
expression (13) 13
genes, tumor suppressor (13) 13
amino acid sequence (12) 12
chromosomes (12) 12
chromosomes, artificial, yeast (12) 12
dna (12) 12
menin (12) 12
protein (12) 12
abridged index medicus (11) 11
biochemistry (11) 11
breast neoplasms - genetics (11) 11
chromosomes, human, pair 11 - genetics (11) 11
congenital, hereditary, and neonatal diseases and abnormalities (11) 11
endocrine neoplasia type-1 (11) 11
genetic mapping (11) 11
genomes (11) 11
multidisciplinary sciences (11) 11
parathyroid tumors (11) 11
polymorphism, genetic (11) 11
polymorphism, single nucleotide (11) 11
biotechnology & applied microbiology (10) 10
endocrine system diseases (10) 10
exons (10) 10
heterozygote (10) 10
men1 (10) 10
microbiology (10) 10
multiple endocrine neoplasia (10) 10
neoplasm proteins - metabolism (10) 10
neoplasms (10) 10
phenotype (10) 10
transcription (10) 10
beer (9) 9
cell line (9) 9
chemistry (9) 9
chromosomes, human, pair 11 (9) 9
cloning (9) 9
compositions or test papers therefor (9) 9
condition-responsive control in microbiological orenzymological processes (9) 9
dna primers (9) 9
endocrine system (9) 9
endocrinology & metabolism (9) 9
enzymology (9) 9
gene deletion (9) 9
gene mutations (9) 9
identification (9) 9
in situ hybridization, fluorescence (9) 9
localization (9) 9
measuring or testing processes involving enzymes, nucleicacids or microorganisms (9) 9
metallurgy (9) 9
mutation or genetic engineering (9) 9
organic chemistry (9) 9
peptides (9) 9
processes of preparing such compositions (9) 9
spirits (9) 9
vinegar (9) 9
wine (9) 9
zebrafish (9) 9
aged (8) 8
agriculture (8) 8
anemia (8) 8
animal husbandry (8) 8
care of birds, fishes, insects (8) 8
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Molecular Psychiatry, ISSN 1359-4184, 03/2018, Volume 23, Issue 3, pp. 683 - 690
The study of monozygotic twins discordant for attention deficit hyperactivity disorder can elucidate mechanisms that contribute to the disorder, which affects... 
DNA METHYLATION | PSYCHIATRY | BIOCHEMISTRY & MOLECULAR BIOLOGY | PAIRS DISCORDANT | BIPOLAR DISORDER | NEUROSCIENCES | DEFICIT/HYPERACTIVITY DISORDER | COPY-NUMBER-VARIATION | DE-NOVO MUTATIONS | SOMATIC POINT MUTATIONS | PSYCHIATRIC-DISORDERS | DEPRESSIVE DISORDER | GENOME-WIDE ASSOCIATION | Attention Deficit Disorder with Hyperactivity - physiopathology | Diseases in Twins - genetics | Epigenomics | Brain - anatomy & histology | Corpus Striatum - physiopathology | Twins, Monozygotic - genetics | Brain - physiopathology | Humans | Genotype | Male | Neurodevelopmental Disorders - genetics | Cerebellum - physiology | Twins, Monozygotic - psychology | DNA Methylation | Phenotype | Cerebellum - diagnostic imaging | Attention Deficit Disorder with Hyperactivity - diagnostic imaging | Attention Deficit Disorder with Hyperactivity - genetics | Epigenesis, Genetic - genetics | Female | Child | Corpus Striatum - diagnostic imaging | Epigenetic inheritance | Care and treatment | Development and progression | Genetic aspects | Twins | Health aspects | Brain diseases | Cerebellum | Attention deficit disorder | Neuroimaging | Brain | Cerebral cortex | Copy number | Genes | Neurodevelopmental disorders | γ-Aminobutyric acid | Neostriatum | DNA methylation | Children | Probes | Deoxyribonucleic acid--DNA | Medical imaging | Brain architecture | Dopamine | DNA probes | Serotonin | Attention deficit hyperactivity disorder | Cortex | Discordance | Anatomy | Neurology | Epigenetics | Methylation | Index Medicus
Journal Article
PLoS Genetics, ISSN 1553-7390, 12/2018, Volume 14, Issue 12, pp. e1007821 - e1007821
Journal Article
Journal Article
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 1/2001, Volume 98, Issue 3, pp. 1118 - 1123
Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant cancer syndrome, characterized primarily by multiple tumors in the parathyroid glands,... 
Biological Sciences | Pituitary neoplasms | Phenotypes | Introns | Alleles | Heterozygotes | Multiple endocrine neoplasia type 1 | Islets of Langerhans | Embryos | Insulin | Tumors | GASTRULATION | LASER CAPTURE MICRODISSECTION | MEN1 GENE | SUPPRESSOR GENE | PRODUCT | MULTIDISCIPLINARY SCIENCES | MICE | MUTATIONS | HYPERPLASIA | EXPRESSION | PARATHYROID TUMORS | Adenoma - genetics | Exons | Parathyroid Neoplasms - pathology | Humans | Male | Multiple Endocrine Neoplasia Type 1 - genetics | Genes, Lethal | Fetal Death | Hyperparathyroidism - genetics | Recombination, Genetic | Chromosomes, Artificial, Bacterial | Female | Proto-Oncogene Proteins | Neoplasm Proteins - genetics | Genes, Tumor Suppressor | Phosphoglycerate Kinase - genetics | Disease Models, Animal | Islets of Langerhans - pathology | Pancreatic Neoplasms - pathology | Hyperparathyroidism - pathology | Mice, Transgenic | Pancreatic Neoplasms - genetics | Chromosome Mapping | Mice, Inbred Strains | Parathyroid Neoplasms - genetics | Pregnancy | Homozygote | Animals | Multiple Endocrine Neoplasia Type 1 - pathology | Adenoma - pathology | Chromosomes, Human, Pair 11 | Mice | Crosses, Genetic | Endocrine gland cancer | Gene mutations | Islands of Langerhans | Tumor suppressor genes | Parathyroid glands | Genetic aspects | Research | Genetics | Models | Rodents | Cancer | chromosome 11 | MEN1 gene | Multiple endocrine neoplasia 1 | Index Medicus
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 06/2017, Volume 54, Issue 6, pp. 417 - 425
Background Diamond-Blackfan anaemia (DBA) is an inherited bone marrow failure syndrome (IBMFS) characterised by erythroid hypoplasia. It is associated with... 
REGULATOR | DIAGNOSIS | MUTATIONS | GENE | GENETICS & HEREDITY | REGISTRY | Complications and side effects | Usage | Ribosomal proteins | Anemia | Causes of | Biosynthesis | Birth defects | Research | Index Medicus
Journal Article
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 02/2017, Volume 114, Issue 8, pp. 1964 - 1969
Journal Article
Pediatrics, ISSN 0031-4005, 06/2012, Volume 129, Issue 6, pp. e1605 - e1611
Journal Article