English
日本語
signup
login
Repository
Search
Annotators
Editors
Evaluators
NEWS
Documentation
>
top
>
projects
>
DisGeNET5_gene_disease
> docs
DisGeNET5_gene_disease
Documents
(355,496)
JSON
TSV
source DB
source ID
text
size
updated at
# proj.
# Ann.
updated_at
PubMed
15459222
Serial follow-up and the prognostic significance of reverse transcriptase-polymerase chain reaction--staged sentinel lymph nodes from melanoma patients. PURPOSE: Reverse transcriptase-polymerase chain
1.95 KB
2015-11-19
3
8
-
PubMed
18796596
TDP-43 accumulation in inclusion body myopathy muscle suggests a common pathogenic mechanism with frontotemporal dementia. TAR DNA binding protein-43 (TDP-43) is found in ubiquitinated inclusions (UBI
950 Bytes
2015-11-24
3
27
-
PubMed
18248882
Molecular pathology of the FSH receptor: new insights into FSH physiology. Manipulations of mouse genome have helped to elucidate gonadotrophin function but important differences subsist between roden
2.98 KB
2015-11-23
2
3
-
PubMed
2715295
Heterogeneity of serum prolactin throughout the menstrual cycle and pregnancy in hyperprolactinemic women with normal ovarian function. We have demonstrated the selective secretion of high mol wt PRL
2.04 KB
2015-11-27
10
8
-
PubMed
20004480
Catechol-O-methyltransferase Val158Met polymorphism affects therapeutic response to mood stabilizer in symptomatic manic patients. Catechol-O-methyltransferase (COMT) is a candidate gene for the patho
1.38 KB
2015-11-25
4
8
-
PubMed
16554736
Epithelial growth factor receptor status in primary and recurrent ovarian cancer. Success of epidermal growth factor receptor (EGFR) targeting agents in different cancer types is related to EGFR gene
1.21 KB
2015-11-19
3
5
-
PubMed
20197700
Common variant in GRN is a genetic risk factor for hippocampal sclerosis in the elderly. BACKGROUND: Hippocampal sclerosis (HpScl) is common in elderly subjects with dementia, either alone or accompan
1.55 KB
2015-11-25
5
26
-
PubMed
21948299
NUP98 gene fusions and hematopoietic malignancies: common themes and new biologic insights. Structural chromosomal rearrangements of the Nucleoporin 98 gene (NUP98), primarily balanced translocations
1.47 KB
2015-11-26
4
17
-
PubMed
19324937
Previously associated type 2 diabetes variants may interact with physical activity to modify the risk of impaired glucose regulation and type 2 diabetes: a study of 16,003 Swedish adults. OBJECTIVE: R
2.02 KB
2015-11-25
4
17
-
PubMed
23150719
Regulation of mitochondrial oxidative metabolism by tumor suppressor FLCN. BACKGROUND: Birt-Hogg-Dubé (BHD) syndrome is a hereditary hamartoma syndrome that predisposes patients to develop hair follic
2.24 KB
2016-01-11
3
14
-
Page 1