Fig. 10. Expression of the cholinergic receptor subunits Chrna6 and Chrnb3 depends on Pitx3.In situ hybridization for Th, Chrna6 and Chrnb3 on sagittal.

Slides:



Advertisements
Similar presentations
Identification of vegetally localised vrtn transcripts.
Advertisements

Effect on path length by silencing of gustatory-receptor-expressing GRNs. Mean±s.e.m. path lengths are shown. Effect on path length by silencing of gustatory-receptor-expressing.
Structure of abbreviated dystrophins.
Fig. 2. Outline of the two types of stimulus sequences employed in the analysis.(A) Environment information stimuli; (B) adaptation stimuli. Outline of.
Fig. 3. No increase in Tau-mediated toxicity caused by the R406W mutation.(A) GMR-gal4 driving expression from the 68A integration site of 2N4R or 0N4R.
Representative illustrations of a sagittal lung section stained with H&E in a control and a CS-exposed mouse after 6 months. Representative illustrations.
BTN1 mRNA level in response to extracellular pH determined by comparative RT2PCR. BTN1mRNA level in response to extracellular pH determined by comparative.
Fig. 1. Muscle-specific PITX1 over-expression in the Pitx1 transgenic mice.(A) Detection of Pitx1 mRNA expression in muscles of the Pitx1 transgenic mice.
Fig. 3. Knockdown of cited3 results in increased cell death but it does not affect proliferation.Embryos that are injected with the control MO (A–C), cited3.
Fig. 6. Cross-section of the stomach wall and spiral intestine of the embryo, stained with PAS. (A) Surface of the stomach wall (SW) and ingested material.
TC-1 silencing sensitized A549 and SPC-A-1 cells to radiation therapy
Fig. 6. The cholinergic receptor subunits a6 (Chrna6) and b3 (Chrnb3) are (subset) specifically expressed in mdDA neurons during development.(A) The Chrna6.
Fig. 6. Comparison between the response against transformed tissues and capsule formation.At the cellular level the two responses share many similarities.
Fig. 2. Body weight and size analysis of A1/A2-KO mice
Fig. 5. Onecut transcription factors are important for the correct generation of the mdDA neuronal population.(A) Schematic representation of the region.
Fig. 1. Lack of Hmga1 and Hmga2 expression in A1/A2-KO mice
Fig. 4. The model of malate metabolism in fruit cells under different K level conditions. The model of malate metabolism in fruit cells under different.
Fig. 1. Body weight gain in Cbx7-KO mice
Fig. 1. Pigmentation and melanophore counts of rainbow trout parr and smolt caudal fins.Pigmentation of (A) parr and (B) smolt. Pigmentation and melanophore.
Fig. 7. E2F1 acetylation in A1/A2-KO MEFs
TWEAK downregulates SIRT3 in cultured tubular cells and this is prevented by crotonate. TWEAK downregulates SIRT3 in cultured tubular cells and this is.
Fig. 4. Brood size of four successive births by male seahorses Hippocampus erectus in the two groups (TR-1, TR-2).In TR-1 groups: male and female seahorses.
Fig. 4. Targeted disruption of STK35 transcripts in mouse.
Expression data confirm and extend existing knowledge
The abundance and expression of miRNAs.
Fig. 3. Cell-autonomous loss of GABAergic interneurons in the OB of newborn and adult conditional GFRα1 mutants. Cell-autonomous loss of GABAergic interneurons.
Fig. 6. Effect of SAHA and ML on histone acetylation, BAX, and p21CDKN1A expression.PANC-1 and BxPC-3 cells were incubated for 48 hours with 5 µM.
Fig. 2. Soluble sugar and organic acid levels with different K fertilization during fruit development. Soluble sugar and organic acid levels with different.
Fig. 4. BKA values for different species.
Fig. 7. Force–displacement curves from porcine skin.
Loss of serotonergic markers after Smed-pitx RNAi is not due to stem cell-based turnover. Loss of serotonergic markers after Smed-pitx RNAi is not due.
Fig. 6. STK35 KO mice show ovary defects.
Fig. 3. Urinary excretion of Na+ and K+ in WNK3 knockout mice
Distribution and extent of expression.
Statistical chart of significantly differentially expressed genes
Fig. 1. Expression of the five miRNAs encoded by two miRNA clusters in mouse sperm and oocytes.(A) qPCR analyses of levels of miR-16 (positive control),
Fig. 2. Sufficient rate of recombination in embryonic NSCs and NPCs of Emx1cre knock-in mice.(A) Breeding schemes to generate mice with the Emx1cre locus.
2DG downregulates the expression of HIF-1α, PDK1 and c-Myc in NB xenograft. 2DG downregulates the expression of HIF-1α, PDK1 and c-Myc in NB xenograft.
Fig. 11. Chrna6 and Chrnb3 expression depends Pitx3 and Nurr1 but through a different mechanism reported for Vmat2.(A) QPCR analysis of Chrna6 and Chrnb3.
Fig. 4. Expression analysis of Onecut transcription factors during mdDA neuron development.Adjacent coronal sections of E11.5, E12.5 and E13.5 mouse brains.
Fig. 6. The cholinergic receptor subunits a6 (Chrna6) and b3 (Chrnb3) are (subset) specifically expressed in mdDA neurons during development.(A) The Chrna6.
Postnatal expression of dominant-negative FGFR2b causes downregulation of FGFR signaling target genes and changes in expression of dental epithelial markers.
Fig. 5. Upregulation of N. vectensis thrombospondin during regeneration.(A,B) Juvenile polyps were fixed 48 hours following transection and processed.
Expression analysis of periostin in DRG
Fig. 9. Loss of the cholinergic receptor subunit Chrna6 does not alter the development and organization of the mdDA system.(A) In situ hybridization experiments.
Fig. 3. Enhanced EGFR signaling in Rhbdf2P159L/P159L mice.
Fig. 5. Flatworm density and activity on coral polyps
Fig. 2. Tbx1 lineage is largely complementary to the NSD
Representative transverse sections of goldfish liver showing ghs-r1a-positive cells by in situ hybridization. Representative transverse sections of goldfish.
Fig. 12. Overview of the molecular program essential to build mdDA neurons.The genes identified in this study (in red) have been added to the programming.
Effects of Chd1-knockdown on global gene expression.
Morphological changes induced by T3 treatment in trβ crispants
Fig. 3. transparent is required cell-autonomously in iridophores
Fig. 2. Expression of Cx43 mutant T154A resulted in non-radial spreading and formation of protrusions in J558µm3 cells spreading in response to BCR signaling.(A)
Fig. 1. Expression of the five miRNAs encoded by two miRNA clusters in mouse sperm and oocytes.(A) qPCR analyses of levels of miR-16 (positive control),
Expression of smc3 in whole-mount and cryosectioned regenerating fins
Fig. 7. Eye defects in STK35 KO mouse.
Fig. 3. Mean force and velocity during jumping
Fig. 4. Deletion of Baf60c in myocardium results in dilated chambers and impaired cardiac function. Deletion of Baf60c in myocardium results in dilated.
Fig. 2. Temporal map of genes clustering with the expression profile of Lmx1a.(A) Heat-map visualization obtained by HCL of genes clustering with Lmx1a.
Fig. 1. Microarray analyses of genes whose expression is regulated by innervation during synaptogenesis.(A) Schematic drawings of the experimental design.
Fig. 5. Co-expression analyses of disease mutations in YFP-RPGRIP1α1 with wild-type RFP-RPGR1–19 or RFP-RPGRORF15 in COS7 cells.YFP-RPGRIP1α1 with disease-associated.
Table 1. Measurement of ring diameters of proteins localizing in ring-like patterns around centrioles.Consideration of the size of IgG (about 8 nm) raises.
Fig. 7. Nrf2-dependent enzyme activities in wild-type, Nrf2- and Keap1-deficient tissues.Hepatic (A,C,E) and cortical (B,D,F) enzyme activities of NQO1.
Fig. 1. Lhx1 is expressed in the proximal region of the OV
Fig. 5. Behaviours of the wild-types Oregon-R at two temperatures.
Phenotypic analysis of the CNS in mutants for Ror, otk and otk2
Fig. 3. Changes in the total EPS/Chl a ratio and bend interval of trichomes before and after the removal of polysaccharide from the BG11-cultured N. flagelliforme.
Fig. 8. Expression of other genomic-clustered Chrn subunits in the mesodiencephalon.(A) Schematic representation illustrating the assembly of the Chrnb4,
Identification of a novel subset of mDA neurons in the VTA that expresses Neurod6, OTX2, CALBINDIN1, ALDH1A1, and Grp. Identification of a novel subset.
Presentation transcript:

Fig. 10. Expression of the cholinergic receptor subunits Chrna6 and Chrnb3 depends on Pitx3.In situ hybridization for Th, Chrna6 and Chrnb3 on sagittal sections of Pitx3+/+ and Pitx3−/− mice. Expression of the cholinergic receptor subunits Chrna6 and Chrnb3 depends on Pitx3.In situ hybridization for Th, Chrna6 and Chrnb3 on sagittal sections of Pitx3+/+ and Pitx3−/− mice. The expression of Chrna6 is prominently downregulated in a medial subset of mdDA neurons as a consequence of Pitx3 ablation, whereas the transcript of Chrnb3 could not be detected in any mdDA neurons in Pitx3−/− mice. L, lateral; M, medial. Koushik Chakrabarty et al. Biology Open 2012;1:693-704 © 2012. Published by The Company of Biologists Ltd