Aperçu des produits pour anti-Sonic Hedgehog (SHH) Anticorps

Human Sonic Hedgehog (SHH) interaction partners

1. Histone deacetylase 6 (HDAC6 (Montrer HDAC6 Anticorps)) inhibition enhanced glioma stem cells (GSCs) radiosensitivity via inactivating sonic hedgehog protein (SHH)/glioma-associated oncogene homolog (Montrer GLI1 Anticorps) 1 (Gli1 (Montrer GLI1 Anticorps)) pathway.

2. Blockade of the Shh signaling pathway could reduce cell proliferation and migration only in MDA-MB-231 cells. Hh pathway inhibitor-1 (Montrer PPP1R1A Anticorps) (HPI-1) increased the percentages of late apoptotic cells in MDA-MB-231 cells and early apoptotic cells in T2 cells

3. Structure-guided mutational analysis shows that interaction between ShhN and Ptch1 (Montrer PTCH1 Anticorps) is steroid-dependent.

4. Protease nexin-1 (Montrer SERPINE2 Anticorps) prevents growth of human B cell lymphoma via inhibition of sonic hedgehog signaling.

5. SHH-related signaling pathway affects antineoplastic drug resistance in cultured glioma cells.

6. SHH is expressed in cilia in the airway epithelial cells.SHH may mediate noncanonical hedgehog signaling through motile cilia to dampen respiratory defenses.

7. High SHH expression is associated with radioresistance in esophageal adenocarcinoma.

8. Identify SMO-dependent Shh signalling as a specific process for the activation of adventitial fibroblasts and the subsequent proliferation of smooth muscle cells and neointima formation.

9. In conclusion, our data suggest that overexpression of the Hedgehog components SHH, GLI2 (Montrer GLI2 Anticorps) and FOXA2 (Montrer FOXA2 Anticorps) might be used as markers of an aggressive hemangioma.

10. These findings showed the upexpression of sonic hedgehog and vascular endothelial growth factor (Montrer VEGF Anticorps) with co-localization in varicocele veins which imply that the reducing hypoxia or using sonic hedgehog antagonists may be helpful for this vascular disease.

Mouse (Murine) Sonic Hedgehog (SHH) interaction partners

1. Results suggest distinct functions of tuberous sclerosis complex 1 protein (Tsc1 (Montrer TSC1 Anticorps)) and tuberous sclerosis complex 2 protein (Tsc2 (Montrer TSC2 Anticorps)) in cellular signaling as the two genes affect ciliary length control and sonic hedgehog protein signaling via different mechanisms.

2. The results of this study indicated that Shh, Sfrp1 (Montrer SFRP1 Anticorps), and Wnt5a (Montrer WNT5A Anticorps) collaborate to direct the pathfinding of descending 5-HT (Montrer DDC Anticorps) axons in the brainstem.

3. data illustrate that persistent Hh signaling in the palatal epithelium contributes to the etiology and pathogenesis of submucous cleft palate through its interaction with a p63 (Montrer CKAP4 Anticorps)/Irf6 (Montrer IRF6 Anticorps)-dependent biological regulatory loop and through a p63 (Montrer CKAP4 Anticorps)-induced cell adhesion network.

4. SOX2 (Montrer SOX2 Anticorps) functions downstream of HH signaling to regulate lingual epithelium homeostasis.

5. High SHH expression is associated with medulloblastoma formation.

6. Identify SMO-dependent Shh signalling as a specific process for the activation of adventitial fibroblasts and the subsequent proliferation of smooth muscle cells and neointima formation.

7. In the mutant Hammer toe (Hm) genome, a 150-kb noncoding DNA fragment from chromosome 14 is inserted into the region upstream of the Sonic hedgehog (Shh) promoter in chromosome 5. Two different regions are necessary for the syndactyly phenotype of Hm.

8. Data show that Sonic hedgehog (Shh), which encodes a secreted protein signal, is expressed in the sensory neurons, and that experimental ablation of neuronal Shh expression causes loss of taste receptor cells (TRCs).

9. Here by inducing expression of constitutively active Smoothened (SmoM2) or Gli2 (Montrer GLI2 Anticorps) (DeltaNGli2) in the adipocyte lineage of postnatal mice, the authors show that targeted activation of Hedgehog signaling suppresses high-fat-diet-induced obesity and improves whole-body glucose tolerance and insulin (Montrer INS Anticorps) sensitivity.

10. These data suggest a potential novel mechanism in which alterations in SHH variance during evolution may have driven changes in limb patterning and digit length.

Zebrafish Sonic Hedgehog (SHH) interaction partners

1. Mutation of hmgcs1 (Montrer HMGCS1 Anticorps) 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 (Montrer GLI1 Anticorps), a known Shh target gene, at 4 dpf, after morphological deficits in craniofacial development and chondrocyte differentiation were observed in hmgcs1 (Montrer HMGCS1 Anticorps) mutants.

2. Shha/Smo is functionally dedicated to ray branching during fin regeneration.

3. Shh and Rx3 govern formation of a distinct progenitor domain that elaborates patterning through its anisotropic growth and differentiation.

4. Time-lapse imaging revealed that knockdown of miR (Montrer MYLIP Anticorps)-219 function accelerates the growth of primary cilia, revealing a possible mechanistic link between miR (Montrer MYLIP Anticorps)-219-mediated regulation of apical Par (Montrer AFG3L2 Anticorps) proteins and Shh signaling.

5. Shh is not essential for the early activation of has2 (Montrer HAS2 Anticorps), but supports proper chondrogenic differentiation.

6. Opposing Shh and Fgf signals initiate nasotemporal patterning of the zebrafish retina.

7. Hedgehog signaling has a role in dental papilla formation and tooth size during zebrafish odontogenesis

8. Data indicate that the transgenic lines report Hedgehog pathway state in individual cells and with high sensitivity.

9. We further demonstrate that the elevated Hedgehog signaling in Sox11 (Montrer SOX11 Anticorps)-deficient zebrafish was caused by a large increase in shha transcription; indeed, suppressing Shha expression rescued the ocular phenotypes of sox11 (Montrer SOX11 Anticorps) morphants.

10. Pax6 (Montrer PAX6 Anticorps) has an evolutionarily conserved function in establishing the temporospatial expression of Shh in the mid-diencephalic organizer in vertebrates.

Xenopus laevis Sonic Hedgehog (SHH) interaction partners

1. SHH-dependent E-ligase Midline1 (Montrer MID1 Anticorps) regulates ubiquitin-mediated proteasomal degradation of Pax6 (Montrer PAX6 Anticorps) during visual system development.

2. Data indicate that sonic hedgehog is expressed exclusively in the notochord but not in the spinal cord of the regenerate.

3. Dzip1 (Montrer DZIP1 Anticorps)-dependent stabilization of Spop/HIB is evolutionarily conserved and essential for proper regulation of Gli (Montrer GLI1 Anticorps)/Ci proteins in the Hh pathway.

4. Notch (Montrer NOTCH1 Anticorps) signaling promotes floor plate and hypochord fates over notochord, but has variable effects on Shh expression in the midline.

5. These results indicate that electrical activity and second-messenger signaling mediate Shh action in embryonic spinal neurons.

6. Connective tissue-specific expression of BMP-4 (Montrer BMP4 Anticorps) mRNA is up-regulated by sonic hedgehog.

7. In an examination of signaling pathways in developing Xenopus lung, shh but not ihh (Montrer IHH Anticorps) was expressed in the very anterior part of early lung epithelium.

8. Data propose that Shh serves as a ventral optic tract repellent that helps to define the caudal (Montrer CAD Anticorps) boundary for retinal axons in the diencephalon, and that this signaling is also required for initial target recognition at the optic tectum.

9. The forebrain of Xenopus revealed a largely conserved pattern of Shh expression among tetrapods.

10. Hedgehog regulates superficial slow muscle fibres in Xenopus and tetrapod trunk myogenesis

Cow (Bovine) Sonic Hedgehog (SHH) interaction partners

1. study shows evolutionary alteration of a Ptch1 (Montrer PTCH1 Anticorps) cis (Montrer CISH Anticorps)-regulatory module, which no longer responds to graded SHH signalling during bovine handplate development

Guinea Pig Sonic Hedgehog (SHH) interaction partners

1. Shh signaling pathway induces myopic development by activating MMP-2 (Montrer MMP2 Anticorps) in guinea pigs