Reduced systolic function
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
Keratoderma, Palmoplantar
|
0.100 |
Biomarker
|
disease |
HPO |
|
|
|
Ventricular Arrhythmia, CTCAE 5.0
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
Leukemia, Myelocytic, Acute
|
0.010 |
Biomarker
|
disease |
BEFREE |
A new human diploid cell line, designated PLB-985, has been established from the peripheral blood of a patient with acute nonlymphocytic leukemia (ANLL).
|
3475136 |
1987 |
Congestive heart failure
|
0.400 |
AlteredExpression
|
disease |
BEFREE |
In contrast, steady-state levels of phospholamban mRNA decreased, whereas levels of beta-myosin heavy-chain mRNA were unchanged with heart failure.
|
2040039 |
1991 |
Heart failure
|
0.300 |
AlteredExpression
|
disease |
BEFREE |
In contrast, steady-state levels of phospholamban mRNA decreased, whereas levels of beta-myosin heavy-chain mRNA were unchanged with heart failure.
|
2040039 |
1991 |
Cardiomyopathies
|
0.700 |
Biomarker
|
group |
CLINGEN |
Identification of regions in the Ca(2+)-ATPase of sarcoplasmic reticulum that affect functional association with phospholamban.
|
8428955 |
1993 |
HIV-1 infection
|
0.010 |
Biomarker
|
disease |
BEFREE |
The relationship between human immunodeficiency virus type 1 (HIV-1) infection and the induction of NF-kappa B binding activity was examined in a myeloid cell model of HIV-1 infection derived from the PLB-985 cell line.
|
8394446 |
1993 |
Human immunodeficiency virus (HIV) II infection category B1
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
The relationship between human immunodeficiency virus type 1 (HIV-1) infection and the induction of NF-kappa B binding activity was examined in a myeloid cell model of HIV-1 infection derived from the PLB-985 cell line.
|
8394446 |
1993 |
Cardiomyopathies
|
0.700 |
Biomarker
|
group |
CLINGEN |
Targeted ablation of the phospholamban gene is associated with markedly enhanced myocardial contractility and loss of beta-agonist stimulation.
|
8062415 |
1994 |
Cardiomyopathies
|
0.700 |
Biomarker
|
group |
CLINGEN |
Levels of SR proteins involved in calcium release (ryanodine receptor), calcium binding (calsequestrin, calreticulin), and calcium uptake (calcium ATPase, phospholamban) were measured by Western blot analysis in nonfailing human myocardium (n = 7) and in end-stage failing myocardium due to dilated cardiomyopathy (n = 14).
|
7641356 |
1995 |
Cardiomyopathies
|
0.700 |
Biomarker
|
group |
CLINGEN |
Cardiac-specific overexpression of phospholamban alters calcium kinetics and resultant cardiomyocyte mechanics in transgenic mice.
|
8567978 |
1996 |
Congestive heart failure
|
0.400 |
AlteredExpression
|
disease |
BEFREE |
These data also show that the altered SR function in human heart failure cannot be explained by altered protein levels of PLB and SERCA2.
|
8689655 |
1996 |
Heart failure
|
0.300 |
AlteredExpression
|
disease |
BEFREE |
These data also show that the altered SR function in human heart failure cannot be explained by altered protein levels of PLB and SERCA2.
|
8689655 |
1996 |
Cardiomyopathy, Dilated
|
0.200 |
AlteredExpression
|
group |
BEFREE |
Sarcoplasmic reticulum Ca2+ATPase and phospholamban mRNA and protein levels in end-stage heart failure due to ischemic or dilated cardiomyopathy.
|
8862513 |
1996 |
Cardiomyopathy, Familial Idiopathic
|
0.100 |
AlteredExpression
|
disease |
BEFREE |
Significantly lower levels of SR Ca2+ATPase mRNA levels (55% and -56%, P < 0.001 for DCM and ICM, respectively) and phospholamban mRNA (45%, P < 0.001 for DCM; 31%, P < 0.05 for ICM) were observed in failing than in nonfailing myocardium.
|
8862513 |
1996 |
Cardiomyopathy, Familial Idiopathic
|
0.100 |
AlteredExpression
|
disease |
BEFREE |
We determined mRNA and/or protein levels for PLB and SERCA2 in the same left ventricular tissue of patients undergoing heart transplantation due to idiopathic dilated cardiomyopathy (IDC) or ischemic cardiomyopathy (ICM) in comparison to left ventricular tissue from nonfailing human hearts (NF).
|
8689655 |
1996 |
End stage cardiac failure
|
0.030 |
AlteredExpression
|
disease |
BEFREE |
Sarcoplasmic reticulum Ca2+ATPase and phospholamban mRNA and protein levels in end-stage heart failure due to ischemic or dilated cardiomyopathy.
|
8862513 |
1996 |
Ischemic cardiomyopathy
|
0.020 |
AlteredExpression
|
disease |
BEFREE |
We determined mRNA and/or protein levels for PLB and SERCA2 in the same left ventricular tissue of patients undergoing heart transplantation due to idiopathic dilated cardiomyopathy (IDC) or ischemic cardiomyopathy (ICM) in comparison to left ventricular tissue from nonfailing human hearts (NF).
|
8689655 |
1996 |
Ischemic cardiomyopathy
|
0.020 |
AlteredExpression
|
disease |
BEFREE |
Significantly lower levels of SR Ca2+ATPase mRNA levels (55% and -56%, P < 0.001 for DCM and ICM, respectively) and phospholamban mRNA (45%, P < 0.001 for DCM; 31%, P < 0.05 for ICM) were observed in failing than in nonfailing myocardium.
|
8862513 |
1996 |
Myofibrillar Myopathy
|
0.010 |
Biomarker
|
disease |
BEFREE |
We observed a match between myofibrillar changes and changes in SR membrane markers specific to fiber type, i.e. the fast (SERCA1) Ca(2+)-ATPase isoform increased concomitantly with a decrease of protein phospholamban (PLB), which in native SR membranes colocalizes with the slow (SERCA2a) SR Ca(2+)-ATPase, and regulates its activity depending on phosphorylation by protein kinases.
|
8845717 |
1996 |
Cardiomyopathies
|
0.700 |
Biomarker
|
group |
CLINGEN |
Transgenic approaches to define the functional role of dual site phospholamban phosphorylation.
|
9468536 |
1998 |
Congestive heart failure
|
0.400 |
Biomarker
|
disease |
BEFREE |
The potential physiological relevance of PLB function in human heart failure is also covered.
|
9790566 |
1998 |
Heart failure
|
0.300 |
Biomarker
|
disease |
BEFREE |
The potential physiological relevance of PLB function in human heart failure is also covered.
|
9790566 |
1998 |
Cardiomyopathies
|
0.700 |
Biomarker
|
group |
CLINGEN |
The human phospholamban gene: structure and expression.
|
10198197 |
1999 |