×
Entrez Id:
54704
Gene Symbol:
PDP1
PDP1
Acidosis
0.010
Biomarker
LHGDN
Pyruvate dehydrogenase phosphatase deficiency: a cause of congenital chronic lactic acidosis in infancy.
172850
1975
×
Entrez Id:
133418
Gene Symbol:
EMB
EMB
Embryonal Carcinoma
0.010
Biomarker
LHGDN
A teratocarcinoma glycoprotein carrying a developmentally regulated carbohydrate marker is a member of the immunoglobulin gene superfamily.
2963822
1988
×
Entrez Id:
3718
Gene Symbol:
JAK3
JAK3
Severe Combined Immunodeficiency
0.700
GeneticVariation
LHGDN
Here we investigate two unrelated T- B+ SCID patients (both from consanguineous parents) who have homozygous mutations in the gene for Jak-3 .
7659163
1995
×
Entrez Id:
4534
Gene Symbol:
MTM1
MTM1
Congenital Structural Myopathy
0.400
GeneticVariation
LHGDN
A gene mutated in X-linked myotubular myopathy defines a new putative tyrosine phosphatase family conserved in yeast.
8640223
1996
×
Entrez Id:
11013
Gene Symbol:
TMSB15A
TMSB15A
Prostatic Neoplasms
0.010
AlteredExpression
LHGDN
Thymosin beta 15: a novel regulator of tumor cell motility upregulated in metastatic prostate cancer.
8946830
1996
×
Entrez Id:
7447
Gene Symbol:
VSNL1
VSNL1
Glioma
0.010
Biomarker
LHGDN
The neuronal calcium-sensor protein VILIP modulates cyclic AMP accumulation in stably transfected C6 glioma cells: amino-terminal myristoylation determines functional activity.
9109541
1997
×
Entrez Id:
1962
Gene Symbol:
EHHADH
EHHADH
Hepatomegaly
0.010
GeneticVariation
LHGDN
Pathology of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency caused by the G1528C mutation.
9185222
1997
×
Entrez Id:
6638
Gene Symbol:
SNRPN
SNRPN
Prader-Willi Syndrome
0.800
Biomarker
LHGDN
Mice harbouring an intragenic deletion in Snrpn are phenotypically normal, suggesting that mutations of SNRPN are not sufficient to induce PWS .
9590284
1998
×
Entrez Id:
5074
Gene Symbol:
PAWR
PAWR
Alzheimer's Disease
0.070
AlteredExpression
LHGDN
Par-4 expression was enhanced, and mitochondrial dysfunction and apoptosis exacerbated, in cells expressing presenilin-1 mutations associated with early-onset inherited AD .
9701251
1998
×
Entrez Id:
1039
Gene Symbol:
CDR2
CDR2
Paraneoplastic Cerebellar Degeneration
0.090
Biomarker
LHGDN
Tumor-specific killer cells in paraneoplastic cerebellar degeneration.
9809559
1998
×
Entrez Id:
3135
Gene Symbol:
HLA-G
HLA-G
Colonic Neoplasms
0.010
Biomarker
LHGDN
Increased expression of human histocompatibility leukocyte antigen-G in colorectal cancer cells.
9855710
1998
×
Entrez Id:
3135
Gene Symbol:
HLA-G
HLA-G
Colorectal Neoplasms
0.010
Biomarker
LHGDN
Increased expression of human histocompatibility leukocyte antigen-G in colorectal cancer cells.
9855710
1998
×
Entrez Id:
1890
Gene Symbol:
TYMP
TYMP
Stomach Neoplasms
0.340
AlteredExpression
LHGDN
Thymidine phosphorylase activity in tumor correlates with venous invasion.
9857235
1998
×
Entrez Id:
7258
Gene Symbol:
TSPY1
TSPY1
Gonadoblastoma
0.100
GeneticVariation
LHGDN
Gonadoblastoma , testicular and prostate cancers, and the TSPY gene.
10090875
1999
×
Entrez Id:
7258
Gene Symbol:
TSPY1
TSPY1
Prostatic Neoplasms
0.020
GeneticVariation
LHGDN
Gonadoblastoma, testicular and prostate cancers, and the TSPY gene.
10090875
1999
×
Entrez Id:
51586
Gene Symbol:
MED15
MED15
AIDS related complex
0.010
AlteredExpression
LHGDN
Composite co-activator ARC mediates chromatin-directed transcriptional activation.
10235267
1999
×
Entrez Id:
7534
Gene Symbol:
YWHAZ
YWHAZ
Neurodegenerative Disorders
0.040
Biomarker
LHGDN
alpha-Synuclein shares physical and functional homology with 14-3-3 proteins.
10407019
1999
×
Entrez Id:
7534
Gene Symbol:
YWHAZ
YWHAZ
Parkinson Disease
0.030
Biomarker
LHGDN
alpha-Synuclein shares physical and functional homology with 14-3-3 proteins.
10407019
1999
×
Entrez Id:
2950
Gene Symbol:
GSTP1
GSTP1
Chronic Obstructive Airway Disease
0.100
GeneticVariation
LHGDN
Genetic polymorphism of exon 5 of GSTP1 may be associated with COPD because the GSTP1 /Ile105 genotype is predominantly found in COPD .
10413721
1999
×
Entrez Id:
581
Gene Symbol:
BAX
BAX
leukemia
0.080
AlteredExpression
LHGDN
Ionizing radiation-induced, Bax-mediated cell death is dependent on activation of cysteine and serine proteases.
10437917
1999
×
Entrez Id:
274
Gene Symbol:
BIN1
BIN1
melanoma
0.020
GeneticVariation
LHGDN
Our findings suggest that aberrant splicing of Bin1 may contribute to melanoma progression, and they define a mechanism by which the activity of a tumor suppressor can be eliminated in cells.
10449755
1999
×
Entrez Id:
1039
Gene Symbol:
CDR2
CDR2
Paraneoplastic Cerebellar Degeneration
0.090
Biomarker
LHGDN
Paraneoplastic cerebellar degeneration (PCD) is a disorder in which breast or ovarian tumors express an onconeural antigen termed cdr2 , which normally is expressed in cerebellar Purkinje neurons.
10465786
1999
×
Entrez Id:
64319
Gene Symbol:
FBRS
FBRS
Fibrosis
0.010
Biomarker
LHGDN
Fibrosin was not detected in control rats not exhibiting fibrosis .
10493891
1999
×
Entrez Id:
25802
Gene Symbol:
LMOD1
LMOD1
Hyperthyroidism
0.010
AlteredExpression
LHGDN
The 64kD human autoantigen D1 is expressed in slow fibers of extraocular and sternothyroid muscles as a component of myofibrils, and is not upregulated in conditions of hyperthyroidism .
10520227
1999
×
Entrez Id:
6376
Gene Symbol:
CX3CL1
CX3CL1
Encephalitis
0.010
AlteredExpression
LHGDN
Neuronal fractalkine expression in HIV-1 encephalitis: roles for macrophage recruitment and neuroprotection in the central nervous system.
10640747
2000