Malignant neoplasm of lung
|
0.010 |
Biomarker
|
disease |
BEFREE |
In an effort to develop a biomarker for lung cancer risk, we evaluated the transcript expressions of 14 antioxidant, DNA repair, and transcription factor genes in normal bronchial epithelial cells (HUGO names CAT, CEBPG, E2F1, ERCC4, ERCC5, GPX1, GPX3, GSTM3, GSTP1, GSTT1, GSTZ1, MGST1, SOD1, and XRCC1).
|
19887610 |
2009 |
Carcinoma of lung
|
0.010 |
Biomarker
|
disease |
BEFREE |
In an effort to develop a biomarker for lung cancer risk, we evaluated the transcript expressions of 14 antioxidant, DNA repair, and transcription factor genes in normal bronchial epithelial cells (HUGO names CAT, CEBPG, E2F1, ERCC4, ERCC5, GPX1, GPX3, GSTM3, GSTP1, GSTT1, GSTZ1, MGST1, SOD1, and XRCC1).
|
19887610 |
2009 |
Primary malignant neoplasm of lung
|
0.010 |
Biomarker
|
disease |
BEFREE |
In an effort to develop a biomarker for lung cancer risk, we evaluated the transcript expressions of 14 antioxidant, DNA repair, and transcription factor genes in normal bronchial epithelial cells (HUGO names CAT, CEBPG, E2F1, ERCC4, ERCC5, GPX1, GPX3, GSTM3, GSTP1, GSTT1, GSTZ1, MGST1, SOD1, and XRCC1).
|
19887610 |
2009 |
Frontotemporal Lobar Degeneration
|
0.010 |
Biomarker
|
disease |
BEFREE |
Mutations in the gene encoding granulin (HUGO gene symbol GRN, also referred to as progranulin, PGRN), located at chromosome 17q21, were recently linked to tau-negative ubiquitin-positive frontotemporal lobar degeneration (FTLDU).
|
18543312 |
2008 |
GRN-related frontotemporal dementia
|
0.010 |
Biomarker
|
disease |
BEFREE |
Mutations in the gene encoding granulin (HUGO gene symbol GRN, also referred to as progranulin, PGRN), located at chromosome 17q21, were recently linked to tau-negative ubiquitin-positive frontotemporal lobar degeneration (FTLDU).
|
18543312 |
2008 |
Ectodermal Dysplasia
|
0.010 |
Biomarker
|
disease |
BEFREE |
Alterations in nuclear factor kappa B (NF-kappaB) essential modulator (NEMO; HUGO-approved symbol IKBKG) underlie most cases of ectodermal dysplasia with immune deficiency (EDI), a human disorder characterized by anhidrosis with diminished immunity.
|
18412279 |
2008 |
Albinism, Ocular
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
An intronic point mutation was identified in the ocular albinism type 1 (OA1) gene (HUGO symbol, GPR143) in a family with the X-linked form of ocular albinism.
|
16550551 |
2006 |
Peutz-Jeghers Syndrome
|
0.010 |
Biomarker
|
disease |
BEFREE |
The human LKB gene (official HUGO symbol, STK11) encodes a serine/threonine protein kinase that is defective in patients with Peutz-Jeghers syndrome (PJS).
|
16110486 |
2005 |
Malignant Neoplasms
|
0.020 |
GeneticVariation
|
group |
BEFREE |
INI1hSNF5 (HUGO symbol: SMARCB1), located at 22q11, encodes a component of the ATP-dependent chromatin remodeling hSWI-SNF complex; it is a tumor suppressor gene that is mutated in several malignant tumors.
|
15993274 |
2005 |
Neoplasms
|
0.020 |
Biomarker
|
group |
BEFREE |
INI1hSNF5 (HUGO symbol: SMARCB1), located at 22q11, encodes a component of the ATP-dependent chromatin remodeling hSWI-SNF complex; it is a tumor suppressor gene that is mutated in several malignant tumors.
|
15993274 |
2005 |
Bipolar Disorder
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
We performed a case/control study on the DAT1 (HUGO approved symbol SL6A3) gene core promoter polymorphism -67A/T to analyze the possible association of either allele of this polymorphism with bipolar disorder.
|
15768394 |
2005 |
Prostate carcinoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
Only four genes (ITM2B, CHC1L, KIAA0970, and LOC51131), located in the region most frequently deleted in prostate carcinoma, showed a significant difference in expression between normal and neoplastic prostate tissues.
|
12886522 |
2003 |
Retinoschisis
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
The XLRS1 gene (HUGO-approved symbol, RS1) has been found to cause X-linked recessive retinoschisis (RS) which is characterized by splitting of the superficial layer of the retina.
|
10220153 |
1999 |
Psoriasis
|
0.110 |
GeneticVariation
|
disease |
BEFREE |
The existence of a psoriasis susceptibility locus, PSORS1 (HUGO/GDB-approved symbol), in or near the HLA region of chromosome 6 is strongly supported by a lod score analysis of HLA-B and psoriasis in 97 families from 16 published datasets.
|
9694251 |
1998 |