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anti-Mouse (Murine) WNT1 Antibodies:
anti-Human WNT1 Antibodies:
anti-Rat (Rattus) WNT1 Antibodies:
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Human Polyclonal WNT1 Primary Antibody for IF (p), IHC (p) - ABIN733748
Gao, Liu, Chen, Lv, Wu, Mi, Wang: Comparative study of Hsp27, GSK3?, Wnt1 and PRDX3 in Hirschsprung's disease. in International journal of experimental pathology 2014
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Human Polyclonal WNT1 Primary Antibody for WB - ABIN3042350
Dong, Duan, Han, Zhang, Wu: Suppression of wingless-type MMTV integration site family, member 1 expression by small interfering RNA inhibits U251 glioma cell growth in vitro. in Oncology letters 2014
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Human Polyclonal WNT1 Primary Antibody for WB - ABIN4886766
Mi, Li, Zhang, Zhao, Peng, Yang, Zheng: MicroRNA-139-5p regulates C2C12 cell myogenesis through blocking Wnt/β-catenin signaling pathway. in Biochemistry and cell biology = Biochimie et biologie cellulaire 2015
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Human Monoclonal WNT1 Primary Antibody for ICC, FACS - ABIN969458
Toffart, Moro-Sibilot, Couraud, Merle, Perol, Girard, Souquet, Mastroianni, Ferretti, Romand, Chatellain, Vesin, Brambilla, Brambilla, Timsit: Evaluation of RECIST in chemotherapy-treated lung cancer: the Pharmacogenoscan Study. in BMC cancer 2015
Human Polyclonal WNT1 Primary Antibody for ELISA, ICC - ABIN6266035
Tang, Peng, Huang, Xie, Chen, Shen, Gao, You, Xie, Chen: Neoisoliquiritigenin Inhibits Tumor Progression by Targeting GRP78-β- catenin Signaling in Breast Cancer. in Current cancer drug targets 2018
maternal Wnt (show WNT2 Antibodies)/STOP signaling, but not beta-catenin (show CTNNB1 Antibodies) signaling, has a role in cleavage after fertilization and cell cycle progression
sfrp1 (show SFRP1 Antibodies) promotes cardiomyocyte differentiation in Xenopus via negative-feedback regulation of Wnt (show WNT2 Antibodies) signalling.
analysis of differential role of Axin (show AXIN1 Antibodies) RGS (show PITX2 Antibodies) domain function in Wnt (show WNT2 Antibodies) signaling during anteroposterior patterning and maternal axis formation
Data show taht combined Wnt (show WNT2 Antibodies) and Nodal signaling synergistically activates transcription of Spemann organizer genes.
The authors propose that these dual functions of DP1 (show TFDP1 Antibodies) can promote and stabilize biphasic Wnt (show WNT2 Antibodies)-on and Wnt (show WNT2 Antibodies)-off states in response to a gradual gradient of Wnt (show WNT2 Antibodies)/beta-catenin (show CTNNB1 Antibodies) signalling to determine differential cell fates.
aberrant expression of AF1q (show MLLT11 Antibodies) may activate Wnt (show WNT2 Antibodies)/beta-catenin (show CTNNB1 Antibodies) signaling and result in podocyte injury.
These data suggested that Wnt (show WNT2 Antibodies)/beta-catenin (show CTNNB1 Antibodies) pathway might be a potential target to treat the LPS (show TLR4 Antibodies)-induced inflammation in ALI.
Wnt (show WNT2 Antibodies) signaling regulates airway epithelial stem cells in adult murine submucosal glands.
Pax9 (show PAX9 Antibodies)-dependent Wnt (show WNT2 Antibodies) signaling has a role in palatogenesis and cleft palates
Data show that autocrine Wnt (show WNT2 Antibodies) secretion is important for the survival, chromosomal stability, differentiation, and tumorigenic potential of embryonic stem cells (ESCs (show NR2E3 Antibodies)).
Results demonstrated functional differences in the molecular mechanisms downstream of Wnt1 function in the diencephalon, in relation to the spinal cord. Wnt1 signal determines the patterning of the diencephalic dorso-ventral axis
Data show that both transgenic Wnt1-cre and P0-cre are similarly effective in deleting beta-catenin (show CTNNB1 Antibodies) in the neural crest.
data suggest that WNT1-related osteogenesis imperfecta (show COL1A2 Antibodies) and osteoporosis are caused in part by decreased mTORC1-dependent osteoblast function resulting from loss of WNT1 signaling in osteocytes.
Administration of EET alters Wnt1, NOV (show NOV Antibodies), and HO-1 (show HMOX1 Antibodies) signaling to prevent obesity-induced cardiomyopathy in obese mice.
Data indicate that Wnt1 proto-oncogene (show RAB1A Antibodies) protein (WNT1) is the direct target of microRNA miR (show MLXIP Antibodies)-34a in dendritic cell (DC).
MiR (show MLXIP Antibodies)-185 inhibits colon cancer cell proliferation and invasion by targeting Wnt1.
High WNT1 expression is associated with epithelial-mesenchymal transition in gastric cancer.
Biallelic pathogenic splice acceptor site variant (c.359-3C>G) in WNT1 gene located on chromosome 12q13.12 underlying osteogenesis imperfecta (show COL1A2 Antibodies) type 3 in a Pakistani family.
Vertebral compression fractures were present in 78% (7/9) of those aged over 50years but were not seen in younger mutation-positive subjects. All those with fractures had several severely compressed vertebrae. Altogether spinal compression fractures were present in 39% of those with a WNT1 mutation. Only
miR (show MLXIP Antibodies)-218 promoted the apoptosis of human ovarian carcinoma cells via suppression of the WNT (show WNT2 Antibodies)/beta-catenin (show CTNNB1 Antibodies) signaling pathway.
Data suggest that brain imaging be performed in any individual with WNT1-associated osteogenesis imperfecta (show COL1A2 Antibodies) (OI) who also has developmental delay or any neurological deficits.
Data indicate a tetracyclic azafluorenone, SJ26, that is capable of binding to G-quadruplex DNA structure, repressing WNT1 expression, and inhibiting cell migration.
Regulation of WNT (show WNT2 Antibodies) signaling by VSX2 (show VSX2 Antibodies) during optic vesicle patterning in human induced pluripotent stem cells has been described.
High WNT1 expression is associated with metastasis in triple-negative breast cancer.
WNT1 osteoporosis causes significant skeletal changes already in early childhood and impairs bone mass gain during pubertal years.
Data indicate that Wnt-1 protein is present in postdevelopmental endothelial cells where it associates with cytoskeletal elements and may retain function as a tissue polarity gene.
Rspo1-Wnt-VegfC-Vegfr3 signaling plays a crucial role as an endothelial-autonomous permissive cue for developmental angiogenesis.
wnt1 and wnt10b (show WNT10B Antibodies) are required to maintain threshold levels of Pax2.1 and Fgf8 (show FGF8 Antibodies) at the midbrain-hindbrain boundary.
novel role for Wnt (show WNT2 Antibodies)/beta-catenin (show CTNNB1 Antibodies) signalling in determining endocardial cell fate
In zebrafish embryos lacking Wnt3a (show WNT3A Antibodies), Wnt1 and Wnt10b (show WNT10B Antibodies), the expression of engrailed orthologs, pax2a and fgf8 (show FGF8 Antibodies) is not maintained after mid-somitogenesis
two Dvl (show DVL2 Antibodies)-associated paralogs, Dpr1 (show DACT1 Antibodies) and Dpr2 (show DACT2 Antibodies), participate in distinct Wnt (show WNT2 Antibodies)-dependent developmental processes
Wnt (show WNT2 Antibodies)/Axin (show AXIN1 Antibodies)/beta-catenin (show CTNNB1 Antibodies) pathway has a role in ventral CNS development
The boundary and roof plate expression of wnt1 each contribute to upregulation of proneural and delta gene expression and neurogenesis in non-boundary regions.
Epistatic analyses suggest a possible genetic interaction between Wnt (show WNT2 Antibodies)/beta-catenin (show CTNNB1 Antibodies) and Myostatin (show MSTN Antibodies) in regulation of slow and fast twitch muscle myofibrillogenesis
The WNT gene family consists of structurally related genes which encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is a member of the WNT gene family. It is very conserved in evolution, and the protein encoded by this gene is known to be 98% identical to the mouse Wnt1 protein at the amino acid level. The studies in mouse indicate that the Wnt1 protein functions in the induction of the mesencephalon and cerebellum. This gene was originally considered as a candidate gene for Joubert syndrome, an autosomal recessive disorder with cerebellar hypoplasia as a leading feature. However, further studies suggested that the gene mutations might not have a significant role in Joubert syndrome. This gene is clustered with another family member, WNT10B, in the chromosome 12q13 region.
, protein Wnt-1
, proto-oncogene Int-1
, proto-oncogene Wnt-1
, proto-oncogene protein Wnt-1
, proto-oncogene Int-1 homolog
, wingless-type MMTV integration site family, member 1 (oncogene INT1)
, Wingless-type MMTV integration site 1 homolog
, Wingless-type MMTV integration site 1, homolog
, wingless-related MMTV integration site 1
, murine mammary tumor virus integration site
, wingless-type MMTV integration site family member 1