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anti-Human GDNF Antikörper:
anti-Rat (Rattus) GDNF Antikörper:
anti-Mouse (Murine) GDNF Antikörper:
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Rat (Rattus) Polyclonal GDNF Primary Antibody für WB - ABIN3042421
Zhang, Shi, Li, Zhang, Hao: Lipopolysaccharide inhibits the self-renewal of spermatogonial stem cells in vitro via downregulation of GDNF expression in Sertoli cells. in Reproductive toxicology (Elmsford, N.Y.) 2014
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Human Polyclonal GDNF Primary Antibody für ICC, IHC (p) - ABIN3044406
Li, Xia, Zhang, Wu: S100B protein, brain-derived neurotrophic factor, and glial cell line-derived neurotrophic factor in human milk. in PLoS ONE 2011
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Human Polyclonal GDNF Primary Antibody für IF (p), IHC (p) - ABIN736536
Zhang, Cai, Song, Dong, Hou, Lv: Normalization of ventral tegmental area structure following acupuncture in a rat model of heroin relapse. in Neural regeneration research 2014
Human Polyclonal GDNF Primary Antibody für IHC, IP - ABIN4313822
Naudin, Smith, Bond, Dun, Scott, Ashman, Weidenhofer, Roselli: Characterization of the early molecular changes in the glomeruli of Cd151-/-mice highlights induction of mindin and MMP-10. in Scientific reports 1970
Human Polyclonal GDNF Primary Antibody für ELISA, WB - ABIN2473775
Lin, Doherty, Lile, Bektesh, Collins: GDNF: a glial cell line-derived neurotrophic factor for midbrain dopaminergic neurons. in Science (New York, N.Y.) 1993
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We thus confirmed the role of GDNF as an adaptive survival factor, and its alteration appears to have a key role in nephrocalcinosis. We also discovered that, in GDNF-silenced cells, death occurs in a programmed but caspase (zeige CASP3 Antikörper)-independent manner.
The personalization of the patients' treatment using uPA (zeige PRAP1 Antikörper)/PAI-1 (zeige SERPINE1 Antikörper) tumor levels allows the reversion of the well-known poor prognostic impact of high uPA (zeige PRAP1 Antikörper)/PAI-1 (zeige SERPINE1 Antikörper) levels and strongly supports the use of this biomarker in clinical practice.
High Expressions of PLAU (zeige PLAU Antikörper) is associated with lung adenocarcinoma.
Adjuvant chemotherapy was 9% less likely to be recommended by a multidisciplinary board when using the current criteria compared with using a combination of the St. Gallen criteria and Ki67 (zeige MKI67 Antikörper) and uPA (zeige PRAP1 Antikörper)/PAI-1 (zeige SERPINE1 Antikörper) status (P = 0.03). Taken together, our data show discordance among markers in identifying the risk of recurrence, even though each marker may prove to be independently valid.
Results suggested that while alterations at 5:37812784 T > A and 5:37812782 T > A sites related with higher GDNF serum levels and less functionality, and alterations at rs62360370 G > A 3'UTR SNP of GDNF associated with higher severity and lower functionality. However, alterations at both rs2075680 C > A and rs79669773 T > C SNPs affect neither GDNF serum levels nor severity and functionality in bipolar disorder.
To our knowledge, this is the first study which correlates GDNF levels with metabolic parameters. Our results show no differences in GDNF serum level between schizophrenia, a first depressive episode, and healthy controls. GDNF serum level did not correlate with metabolic parameters except for total cholesterol in depression.
The results suggest an interaction between NGF (zeige NGFB Antikörper), GDNF and MMP-9 (zeige MMP9 Antikörper) during the transition to malignancy in prostate cancer (PC). Also this interaction may involve in regulating PC cell differentiation, tumor invasion, progression, and the agressiveness of PC.
Increased expression of uPA (zeige PRAP1 Antikörper) in epidermal cells in psoriasis and in tumor cells in basal cell carcinomas suggests an important role of the uPA (zeige PRAP1 Antikörper) system for aggressively proliferating and invading cells of epidermal origin.
study provides strong support in the role of L. reuteri in suppression of GC cell invasion by downregulation of pathways which is involved in extracellular matrix degradation such as uPA (zeige PRAP1 Antikörper) and uPAR (zeige PLAUR Antikörper)
Study also demonstrates that the interaction between GDNF and proN-cadherin activates specific intracellular signaling pathways; furthermore, GDNF promoted the secretion of matrix metalloproteinase-9 (MMP-9 (zeige MMP9 Antikörper)), which degrades the ECM (zeige MMRN1 Antikörper) via proN-cadherin.
results contradict previous studies suggesting that mammalian GFRalpha1 (zeige GFRA1 Antikörper) and GDNF cannot bind and activate non-mammalian RET (zeige RET Antikörper) and vice versa
the dynamics of glial cell line-derived neurotrophic factor (gdnf) and nitric oxide synthases (nos) mRNA expression in various regions of zebrafish brain
GDNF family ligands including tyrosine kinase receptor (zeige KDR Antikörper) RET (zeige RET Antikörper) are investigated within the adult zebrafish brain.
GDNF is a major determinant of directed neuritic growth , and GDNF acts by promoting local neurite outgrowth.
These results demonstrated the expression of the GDNF receptorial complex in adult zebrafish cerebellum and suggest an autocrine mode of action of GDNF in Purkinje cells.
These results showed that the expression of GDNF is not probably restricted during development but it might be involved in the physiology of adult zebrafish retina.
The expression of glial cell line-derived neurotrophic factor (GDNF) was not restricted to developmental periods but it seems that this factor might be involved in adult zebrafish brain physiology, as observed in mammals.
Analysis of striatal brain samples confirms increased GDNF expression in lentiviral vector-GDNF treated aged animals that correlates with functional improvements and preserved dopaminergic markers, dependent upon GDNF levels.
These results suggest that chronic overexpression of GDNF in brain astrocytes exerts an opposing influence on nigrostriatal dopamine metabolism and neurotransmission.
GDNF promotes self-renewal by blocking differentiation and not by promoting proliferation.
Cross-platform single cell analysis of kidney development shows stromal cells express Gdnf.
Our study provides, for the first time, a global analysis of phosphorylation events in spermatogonial progenitor cells (SPCs) in response to GDNF, and we have identified activation of mTORC1 signaling through ERK kinase-mediated phosphorylation of multiple sites of raptor protein as an important pathway for SPC proliferation.
Data show that NEDL2 regulates GDNF/Ret/Akt pathway depends on its Nedd8 ligase activity rather than ubiquitin ligase activity.
Six2 (zeige SIX2 Antikörper) mediates the protective effects of GDNF on damaged DA neurons by regulating Smurf1 (zeige SMURF1 Antikörper) expression.
Ret (zeige RET Antikörper) is essential to mediate GDNF's neuroprotective and neuroregenerative effect in a Parkinson disease mouse model.
identified IFNg (zeige IFNG Antikörper), Neurturin (Nrtn (zeige NRTN Antikörper)), and glial-derived neurotrophic factor (GDNF) as ligands with unexpected roles in promoting neurogenic differentiation (zeige NEUROD1 Antikörper) of Neural Precursor Cells in vivo.
Using an organ culture system for prostate development and Ret mutant mice, we demonstrate that RET-mediated GDNF signaling in UGS increases proliferation of mesenchyme cells and suppresses androgen-induced proliferation and differentiation of prostate epithelial cells, inhibiting prostate development.
The GDNF-GFRalpha1 (zeige GFRA1 Antikörper) complex is essential for proper hippocampal circuit development.
Spatial expression analysis by whole-mount in situ hybridization showed that the GDNF mRNA was predominantly detected in somites, pronephros, pharyngeal arches, epibranchial placodes, digestive tract and some of the lateral line structure.
This gene encodes a highly conserved neurotrophic factor. The recombinant form of this protein was shown to promote the survival and differentiation of dopaminergic neurons in culture, and was able to prevent apoptosis of motor neurons induced by axotomy. The encoded protein is processed to a mature secreted form that exists as a homodimer. The mature form of the protein is a ligand for the product of the RET (rearranged during transfection) protooncogene. Multiple transcript variants encoding different isoforms have been found for this gene. Mutations in this gene may be associated with Hirschsprung disease.
, plasminogen activator, urinary
, urokinase-type plasminogen activator
, Glial cell line derived neutrophic factor
, astrocyte-derived trophic factor
, glial cell line derived neurotrophic factor
, glial cell line-derived neurotrophic factor
, glial cell line-derived neurotrophic factor long form
, glial cell derived neurotrophic factor
, glial cell-line derived neurotrophic factor
, neurotrophic factor
, glial cell line-derived neurotrophic factor a
, glia-derived neurotrophic growth factor