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anti-Human GLI3 Antibodies:
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Human Polyclonal GLI3 Primary Antibody for ICC, IF - ABIN4314296
Kanda, Mitsuyasu, Nakao, Kawano, Goto, Matsubara, Nakamura: Anti-apoptotic role of the sonic hedgehog signaling pathway in the proliferation of ameloblastoma. in International journal of oncology 2013
Human Polyclonal GLI3 Primary Antibody for ICC, IF - ABIN4314300
Jackson, Smith, Amarsaikhan, Han, Neil, Boi, Vrabel, Tolosa, Almada, Fernandez-Zapico, Elsawa: Modulation of the IL-6 Receptor α Underlies GLI2-Mediated Regulation of Ig Secretion in Waldenström Macroglobulinemia Cells. in Journal of immunology (Baltimore, Md. : 1950) 2015
Dog (Canine) Polyclonal GLI3 Primary Antibody for ELISA - ABIN251265
Haycraft, Banizs, Aydin-Son, Zhang, Michaud, Yoder: Gli2 and Gli3 localize to cilia and require the intraflagellar transport protein polaris for processing and function. in PLoS genetics 2005
Data suggest that negative feedback mediated by GLI3 (GLI (show GLI1 Antibodies)-Kruppel family member) acts to finely tune SHH (sonic hedgehog (show SHH Antibodies)) signaling. During medulloblastoma (MB) formation, nerve tissue cells appear to express nestin (show NES Antibodies) which hyperactivates SHH (show SHH Antibodies) signaling by abolishing negative feedback by GLI3. Restoration of intrinsic negative feedback by repressing nestin (show NES Antibodies) expression represents a promising approach to treat MB. [REVIEW]
the first report of the assessment of the frequency of GLI3/SHH (show SHH Antibodies)/preZRS/ZRS in Chinese polydactyly patients to show any higher possibility of mutations or variants for the 4 genes or sequences in China
Gli3 and Teashirt3 (show ZNF537 Antibodies) might play an important role in the normal development of the ureter.
a novel GLI3 mutation c.714T>A (p.Y238*) was identified in a Chinese family with pre-axial polydactyly. Our results broadened the phenotypic spectrum of GLI3 mutations and demonstrated the feasibility of WES in clinical application of molecular diagnosis.
we describe an ~5 kb deletion within the SHH (show SHH Antibodies) repressor GLI3 in two patients with bilateral tibial hemimelia. This deletion results in a truncated GLI3 protein that lacks a DNA-binding domain and cannot repress hedgehog (show SHH Antibodies) signaling.
2 independent cases of GLI3 morphopathies presented: one is a familial case of Greig Cephalopolysyndactyly Syndrome and the other a non-syndromic case of post-axial polydactyly, both are caused due to a truncation mutation at C-terminal of GLI3
Gene silencing of GLI3 using RNA inference stimulated the growth of human Sertoli cells. miR (show MLXIP Antibodies)-133b promoted the proliferation of human Sertoli cells by targeting GLI3.
We report on a patient with GCPS caused by a novel GLI3 mutation.
Identify mutations tha (show SUFUH Antibodies)t in (show GLI1 Antibodies)crease (show SOX10 Antibodies) GLI activity in patients with Hirschsprung disease.
To date, at least ten loci and four non-syndromic polydactyly-causing genes, including the GLI3 gene, the ZNF141 (show ZNF141 Antibodies) gene, the MIPOL1 (show MIPOL1 Antibodies) gene and the PITX1 (show PITX1 Antibodies) gene, have been identified. (Review)
Gli2 (show GLI2 Antibodies) and Gli3 are dephosphorylated and activated in cilia and that impaired Gli2 (show GLI2 Antibodies) and Gli3 processing in Ta3 (show HSP90B1 Antibodies) mutant is at least in part due to a decrease in Gli2 (show GLI2 Antibodies) and Gli3 phosphorylation.
These results suggest that Tctn1 (show TCTN1 Antibodies), Tctn2 (show TCTN2 Antibodies), and Tctn3 (show TCTN3 Antibodies) are functionally divergent with respect to their role in ciliogenesis and Hedgehog (show SHH Antibodies) signaling but conserved in neural tube patterning and Gli3 processing.
Results indicate that the transcription factor Gli3 (Gli3)-mutant fetal liver (FL) had increased sonic hedgehog (Shh (show SHH Antibodies)) signaling resulting in decreased B cell development.
Our findings show how Nestin (show NES Antibodies) drives hedgehog (show SHH Antibodies) pathway-driven cancers and the tumor-promoting effects of Nestin (show NES Antibodies) were mediated by binding to Gli3, a zinc finger transcription factor (show OSR1 Antibodies) that negatively regulates hedgehog (show SHH Antibodies) signaling.
Gli3 gene is a direct target for repression by Tgifs during the neural tube patterning.
Sufu (show SUFUH Antibodies) is upregulated in active Shh (show SHH Antibodies) responding tissues and accompanies Gli (show GLI1 Antibodies) activators translocating into and Gli (show GLI1 Antibodies) repressors out of the nucleus.
Gli2 (show GLI2 Antibodies)+/-;Gli3Delta699/+ mice can serve as a genetic mouse model for common DSD (show FADS1 Antibodies).
cAMP dependent protein kinase A (PKA) is a key intracellular factor mediating SHH (show SHH Antibodies) signaling through regulation of GLI3 processing.
Despite increased production of full-length GLI2 (show GLI2 Antibodies) and GLI3 isoforms, previously identified GLI (show GLI1 Antibodies) targets important for mandibular and glossal development (Foxf1 (show FOXF1 Antibodies), Foxf2 (show FOXF2 Antibodies), Foxd1 (show FOXD1 Antibodies) and Foxd2 (show FOXD2 Antibodies)) were transcriptionally downregulated in Kif3a (show KIF3A Antibodies)(f/f);Wnt1 (show WNT1 Antibodies)-Cre embryos.
T-box3 interacts with Kif7 (show KIF7 Antibodies) and is required for normal stoichiometry and function of a Kif7 (show KIF7 Antibodies)/Sufu (show SUFUH Antibodies) complex that regulates Gli3 stability and processing.
Zebrafish Gli3 functions as both an activator and a repressor in Hedgehog (show SHH Antibodies) signaling. In the eye, Gli3 is also required for proper ath5 (show ATOH7 Antibodies) expression and the differentiation of retinal ganglion cells.
The results provided evidence that polymorphisms in the GLI3 gene are associated with growth traits, and may be used for marker-assisted selection in beef cattle breeding program.
This gene encodes a protein which belongs to the C2H2-type zinc finger proteins subclass of the Gli family. They are characterized as DNA-binding transcription factors and are mediators of Sonic hedgehog (Shh) signaling. The protein encoded by this gene localizes in the cytoplasm and activates patched Drosophila homolog (PTCH) gene expression. It is also thought to play a role during embryogenesis. Mutations in this gene have been associated with several diseases, including Greig cephalopolysyndactyly syndrome, Pallister-Hall syndrome, preaxial polydactyly type IV, and postaxial polydactyly types A1 and B.
GLI-Kruppel family member GLI3
, glioma-associated oncogene family zinc finger 3
, oncogene GLI3
, transcriptional activator GLI3
, zinc finger protein GLI3
, GLI-Kruppel family member GLI3 (Greig cephalopolysyndactyly syndrome)
, GLI3 full length protein
, neural specific DNA binding protein
, neural-specific DNA-binding protein xGLI3
, GLI-Kruppel family member 3
, GLI3 form of 190 kDa
, anterior digit pattern deformity
, extra toes
, polydactyly Nagoya
, zinc finger transcription factor Gli3
, GLI family zinc finger 3