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anti-Mouse (Murine) Sonic Hedgehog Antikörper:
anti-Human Sonic Hedgehog Antikörper:
anti-Rat (Rattus) Sonic Hedgehog Antikörper:
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Human Polyclonal Sonic Hedgehog Primary Antibody für IF (p), IHC (p) - ABIN731108
Weiss, Guo, Shan, Shi, Romano, Sinha, Cantley, Guo: Brg1 determines urothelial cell fate during ureter development. in Journal of the American Society of Nephrology : JASN 2013
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Human Monoclonal Sonic Hedgehog Primary Antibody für ELISA, WB - ABIN969395
Dierker, Dreier, Migone, Hamer, Grobe: Heparan sulfate and transglutaminase activity are required for the formation of covalently cross-linked hedgehog oligomers. in The Journal of biological chemistry 2009
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Human Monoclonal Sonic Hedgehog Primary Antibody für ELISA, WB - ABIN967021
Lee, Lee, Jung, Park, Park, Hahm: Late reactivation of sonic hedgehog by Helicobacter pylori results in population of gastric epithelial cells that are resistant to apoptosis: implication for gastric carcinogenesis. in Cancer letters 2010
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Human Monoclonal Sonic Hedgehog Primary Antibody für ELISA, FACS - ABIN4355158
Valverde, Pereira, Dias, Guimarães, Ramos, Santos, Gurgel Rocha: Macrophages and endothelial cells orchestrate tumor-associated angiogenesis in oral cancer via hedgehog pathway activation. in Tumour biology 2016
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Human Monoclonal Sonic Hedgehog Primary Antibody für FACS - ABIN4897996
Blotta, Jakubikova, Calimeri, Roccaro, Amodio, Azab, Foresta, Mitsiades, Rossi, Todoerti, Molica, Morabito, Neri, Tagliaferri, Tassone, Anderson, Munshi: Canonical and noncanonical Hedgehog pathway in the pathogenesis of multiple myeloma. in Blood 2012
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Human Monoclonal Sonic Hedgehog Primary Antibody für FACS, IHC - ABIN969567
Kameda, Nakamura, Tanaka, Yamasaki, Kubo, Tanaka, Onishi, Katano: Oestrogen receptor-alpha contributes to the regulation of the hedgehog signalling pathway in ERalpha-positive gastric cancer. in British journal of cancer 2010
Human Polyclonal Sonic Hedgehog Primary Antibody für IHC, ELISA - ABIN1585268
Yang, Liu, Dang, Fang, Tan, Zhao, Xu, Liu: Substance P attenuates hyperoxia‑induced lung injury in neonatal rats. in Molecular medicine reports 2014
Human Polyclonal Sonic Hedgehog Primary Antibody für ICC, IF - ABIN4355160
Palacio-Mancheno, Evashwick-Rogler, Laudier, Purmessur, Iatridis: Hyperosmolarity induces notochordal cell differentiation with aquaporin3 upregulation and reduced N-cadherin expression. in Journal of orthopaedic research : official publication of the Orthopaedic Research Society 1970
Chicken Polyclonal Sonic Hedgehog Primary Antibody für IHC, IHC (p) - ABIN4893080
Lozito, Tuan: Lizard tail skeletal regeneration combines aspects of fracture healing and blastema-based regeneration. in Development (Cambridge, England) 2016
Sonic Hedgehog Activates Phospholipase A2 (zeige YWHAZ Antikörper) to Enhance Smoothened Ciliary Translocation
The Function of SDF-1-CXCR4 Axis in SP Cells-Mediated Protective Role for Renal Ischemia/Reperfusion Injury by SHH/GLI1-ABCG2 Pathway
smaller mvShh conjugates resulted in faster wound resolution compared to the unconjugated Shh. This study is the first to show how the wound healing efficacy of multivalent protein-polymer conjugates is sensitive to the polymer MW, and our findings suggest that this parameter could be used to enhance the efficacy of growth factor conjugates.
SHH can promote cell growth and cell osteoblastic/cementoblastic differentiation via BMP pathway
These studies reveal a postnatal cell population with transient Shh signaling that contributes to oligodendrogenesis during corpus callosum myelination, and gives rise to cells that continue to proliferate in adulthood and contribute to corpus callosum remyelination
These results support a model whereby mutations in Cdon (zeige CDON Antikörper) and prenatal ethanol exposure increase Septo-optic dysplasia risk through spatiotemporal perturbations in Shh signaling activity.
Results report the identification of a novel long-range enhancer for Shh-Shh-brain-enhancer-6 (SBE6)-that is located 100 kb upstream of Shh and that is required for the proper induction of Shh expression during this differentiation program.
neuroectodermal Shh expression, dorsal/ventral patterning, and amount of proliferation in the ventral neuroectoderm was not changed in Wnt1 (zeige WNT1 Antikörper)-Cre;Kif3a (zeige KIF3A Antikörper)(fl/fl (zeige FLT3LG Antikörper)) mutants; however, tissue polarity and directional cell division were disrupted.
The authors find that cholesterol, an important component of the cell membrane, directly binds to Smoothened and changes its shape so that it can activate Hedgehog signaling components inside cells.
Embryonal tumors with multilayered rosettes (ETMRs) are characterized by a parallel activation of Shh and Wnt (zeige WNT2 Antikörper) signaling. Co-activation of these pathways in mouse neural precursors is sufficient to induce ETMR-like tumors in vivo that resemble their human counterparts on the basis of histology and global gene-expression analyses, and that point to apical radial glia cells as the possible tumor cell of origin.
during Hedgehog signaling, ligand binding inhibits Patched (zeige PTCH1 Antikörper) by trapping it in an inactive conformation, a mechanism that explains the dramatically reduced activity of oncogenic Patched1 (zeige PTCH1 Antikörper) mutants.
In an in vitro model of LPS (zeige IRF6 Antikörper) inflammation of the blood-brain barrier, sonic hedgehog signaling was activated by Wip1 (zeige PPM1D Antikörper) overexpression and inhibited by silencing. Wip1 (zeige PPM1D Antikörper) may protect the BBB (zeige ALMS1 Antikörper) against LPS (zeige IRF6 Antikörper) damage via SHH signaling.
the effect gene of the Shh pathway, gli1 (zeige GLI1 Antikörper), was found to have a reduced level of expression along with a decreased expression of gli2 (zeige GLI2 Antikörper).
Findings suggest that oral squamous cell carcinoma (OSCC)derived sonic hedgehog protein (SHH) stimulates angiogenesis at the tumor invasive front.
Expression of SHH and GLI1 (zeige GLI1 Antikörper) may be useful prognostic markers of Merkel cell carcinoma because increased expression was associated with better prognosis.
High SHH expression is associated with esophageal squamous cell carcinoma.
Studies suggest significance of other signaling aside from hedgehog in the pathogenesis of basal cell carcinoma (BCC) of the skin.
Gorlin syndrome-derived induced pluripotent stem cells (iPSCs) expressed lower basal levels than control iPSCs of the genes encoding the Hh ligands Indian Hedgehog (IHH (zeige IHH Antikörper)) and Sonic Hedgehog (SHH).
SHH activation is associated with Rhabdomyosarcoma.
SHH-dependent E-ligase Midline1 (zeige MID1 Antikörper) regulates ubiquitin-mediated proteasomal degradation of Pax6 (zeige PAX6 Antikörper) during visual system development.
Data indicate that sonic hedgehog is expressed exclusively in the notochord but not in the spinal cord of the regenerate.
Dzip1 (zeige DZIP1 Antikörper)-dependent stabilization of Spop (zeige SPOP Antikörper)/HIB is evolutionarily conserved and essential for proper regulation of Gli (zeige GLI1 Antikörper)/Ci proteins in the Hh pathway.
Notch (zeige NOTCH1 Antikörper) signaling promotes floor plate and hypochord fates over notochord, but has variable effects on Shh expression in the midline.
These results indicate that electrical activity and second-messenger signaling mediate Shh action in embryonic spinal neurons.
Connective tissue-specific expression of BMP-4 (zeige BMP4 Antikörper) mRNA is up-regulated by sonic hedgehog.
In an examination of signaling pathways in developing Xenopus lung, shh but not ihh (zeige IHH Antikörper) was expressed in the very anterior part of early lung epithelium.
Data propose that Shh serves as a ventral optic tract repellent that helps to define the caudal (zeige CAD Antikörper) boundary for retinal axons in the diencephalon, and that this signaling is also required for initial target recognition at the optic tectum.
The forebrain of Xenopus revealed a largely conserved pattern of Shh expression among tetrapods.
Hedgehog regulates superficial slow muscle fibres in Xenopus and tetrapod trunk myogenesis
study shows evolutionary alteration of a Ptch1 (zeige PTCH1 Antikörper) cis (zeige CISH Antikörper)-regulatory module, which no longer responds to graded SHH signalling during bovine handplate development
Mutation of hmgcs1 (zeige HMGCS1 Antikörper) had no effect on Shh signaling at 2 and 3 days post fertilization (dpf), but did result in a decrease in the expression of gli1 (zeige GLI1 Antikörper), a known Shh target gene, at 4 dpf, after morphological deficits in craniofacial development and chondrocyte differentiation were observed in hmgcs1 (zeige HMGCS1 Antikörper) mutants.
Shha/Smo is functionally dedicated to ray branching during fin regeneration.
Shh and Rx3 govern formation of a distinct progenitor domain that elaborates patterning through its anisotropic growth and differentiation.
Time-lapse imaging revealed that knockdown of miR (zeige MYLIP Antikörper)-219 function accelerates the growth of primary cilia, revealing a possible mechanistic link between miR (zeige MYLIP Antikörper)-219-mediated regulation of apical Par (zeige AFG3L2 Antikörper) proteins and Shh signaling.
Shh is not essential for the early activation of has2 (zeige HAS2 Antikörper), but supports proper chondrogenic differentiation.
Opposing Shh and Fgf signals initiate nasotemporal patterning of the zebrafish retina.
Hedgehog signaling has a role in dental papilla formation and tooth size during zebrafish odontogenesis
Data indicate that the transgenic lines report Hedgehog pathway state in individual cells and with high sensitivity.
We further demonstrate that the elevated Hedgehog signaling in Sox11 (zeige SOX11 Antikörper)-deficient zebrafish was caused by a large increase in shha transcription; indeed, suppressing Shha expression rescued the ocular phenotypes of sox11 (zeige SOX11 Antikörper) morphants.
Pax6 (zeige PAX6 Antikörper) has an evolutionarily conserved function in establishing the temporospatial expression of Shh in the mid-diencephalic organizer in vertebrates.
This gene encodes a protein that is instrumental in patterning the early embryo. It has been implicated as the key inductive signal in patterning of the ventral neural tube, the anterior-posterior limb axis, and the ventral somites. Of three human proteins showing sequence and functional similarity to the sonic hedgehog protein of Drosophila, this protein is the most similar. The protein is made as a precursor that is autocatalytically cleaved\; the N-terminal portion is soluble and contains the signalling activity while the C-terminal portion is involved in precursor processing. More importantly, the C-terminal product covalently attaches a cholesterol moiety to the N-terminal product, restricting the N-terminal product to the cell surface and preventing it from freely diffusing throughout the developing embryo. Defects in this protein or in its signalling pathway are a cause of holoprosencephaly (HPE), a disorder in which the developing forebrain fails to correctly separate into right and left hemispheres. HPE is manifested by facial deformities. It is also thought that mutations in this gene or in its signalling pathway may be responsible for VACTERL syndrome, which is characterized by vertebral defects, anal atresia, tracheoesophageal fistula with esophageal atresia, radial and renal dysplasia, cardiac anomalies, and limb abnormalities. Additionally, mutations in a long range enhancer located approximately 1 megabase upstream of this gene disrupt limb patterning and can result in preaxial polydactyly.
sonic hedgehog protein
, sonic hedgehog
, hemimelic extra toes
, short digits
, sonic hedgehog homolog
, sonic hedgehog protein A