Fig. 6. The cholinergic receptor subunits a6 (Chrna6) and b3 (Chrnb3) are (subset) specifically expressed in mdDA neurons during development.(A) The Chrna6.

Slides:



Advertisements
Similar presentations
Immunohistochemistry and in situ hybridization allow researchers to pinpoint the expression of their protein and nucleic acid targets, respectively.
Advertisements

Fig. 1. In situ hybridization analysis for detecting endogenous mBest1 transcript in whole-brain region. In situ hybridization results from coronal (top.
Identification of vegetally localised vrtn transcripts.
Intravenous delivery of reovirus to primary and secondary brain tumors
In situ confirmations of Sepw1-enriched genes.
Fig. 2. Outline of the two types of stimulus sequences employed in the analysis.(A) Environment information stimuli; (B) adaptation stimuli. Outline of.
Fig. 8. Esco2-dependent cis-DNA looping model underlying the etiology of RBS. (A) Schematic representation of the cohesin ring complex. Esco2-dependent.
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. The cholinergic receptor subunits a6 (Chrna6) and b3 (Chrnb3) are (subset) specifically expressed in mdDA neurons during development.(A) The Chrna6.
A subset of Trp53CKO fiber cells fail to exit the cell cycle, but express fiber-cell-specific markers. A subset of Trp53CKO fiber cells fail to exit the.
Fig. 4. Induction of a systemic immune response in RasV12-expressing larvae.(A) List of genes that are significantly induced (at q
Fig. 1. Prestin in mouse outer hair cells is localized along the lateral wall of the cell along with β-catenin and Na/K ATPase.Shown are cartoons of the.
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.
Table 2. Cell surface abundance of β1 integrin measured by flow cytometry.DDR wild type and DDR over-expressing cells were treated with deoxymannojirimycin.
Fig. 4. Targeted disruption of STK35 transcripts in mouse.
Expression data confirm and extend existing knowledge
The abundance and expression of miRNAs.
Increased osteoclastogenesis in the mandibular bone of Fgfr2+/S252W embryos at E16.5. Increased osteoclastogenesis in the mandibular bone of Fgfr2+/S252W.
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. 1. Generation of WNK3 knockout mice
Fig. 7. Ror-GFP binds to Myc-tagged Wnts and Wnt receptors.
Fig. 6. STK35 KO mice show ovary defects.
Distribution and extent of expression.
Table 1. Average ± S.E. of level of dissimilarity scores of each feature per stripe per pattern comparison of sides of the same fish (“Same Individual”),
Fig. 2. TSA impairs growth and disrupts morphogenesis of exocrine pancreas in zebrafish larvae with hyperacetylation of nucleosomal histones.WT zebrafish.
GABAergic subtype switch in the absence of Gata2 in the pTh-R precursors. GABAergic subtype switch in the absence of Gata2 in the pTh-R precursors. (A-T)
Statistical chart of significantly differentially expressed genes
The genomic distribution of essential and non-essential mouse genes, separated into known and predicted essentiality. The genomic distribution of essential.
Fig. 4. Quantitative mRNA expression of two membrane-bound trehalase genes in Harmonia axyridis in response to starvation (0–72 h). Quantitative mRNA expression.
prdm1a is co-expressed with foxd3 and tfap2a at the NPB
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.
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. 10. Expression of the cholinergic receptor subunits Chrna6 and Chrnb3 depends on Pitx3.In situ hybridization for Th, Chrna6 and Chrnb3 on sagittal.
Conserved patterns of Shh expression from mammals to teleosts.
Fig. 1. Insufficient rate of recombination in NSCs and NPCs of Nestin-cre transgenic mice.(A) Breeding schemes to generate Nestin-cre transgenic mice (Jax:
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. 5. Flatworm density and activity on coral polyps
Fig. 2. Tbx1 lineage is largely complementary to the NSD
Stage-specific expression modules of preimplantation development.
Fig. 4. Inactivation of Tbx1 and Jag1 with Tbx1Cre results in expanded proneural gene expression. Inactivation of Tbx1 and Jag1 with Tbx1Cre results in.
Fig. 6. IIS affected the soma area of most neurons in pharate adults, but not in larvae.(A,B) Pan-peptidergic expression pattern of 386-Gal4,UAS-CD8::GFP.
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.
The zebrafish swdp75fm and swdp82mf mutations cause exocrine pancreatic hypoplasia and reduced skin pigmentation. The zebrafish swdp75fm and swdp82mf mutations.
Fig. 3. transparent is required cell-autonomously in iridophores
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. 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. 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,
Co-expression of periostin and Sox10 in DRG and DRG explant cultures.
Identification of a novel subset of mDA neurons in the VTA that expresses Neurod6, OTX2, CALBINDIN1, ALDH1A1, and Grp. Identification of a novel subset.
Selective expression of Neurod6 in mDA neurons in the VTA
A tph2 promoter fragment labels DR serotonergic neurons.
Presentation transcript:

Fig. 6. The cholinergic receptor subunits a6 (Chrna6) and b3 (Chrnb3) are (subset) specifically expressed in mdDA neurons during development.(A) The Chrna6 and Chrnb3 genes are organized as a tandem in the mouse genome (chromosome 8) in a tail to tail orientation. The cholinergic receptor subunits a6 (Chrna6) and b3 (Chrnb3) are (subset) specifically expressed in mdDA neurons during development.(A) The Chrna6 and Chrnb3 genes are organized as a tandem in the mouse genome (chromosome 8) in a tail to tail orientation. (B) In situ hybridization (ISH) experiments for Chrna6, Chrnb3 and Th (position control) on sagittal sections of E13.5 mouse brain. The expression patterns of Chrna6 and Chrnb3 are restricted to the mdDA neuronal region and appear to be restricted to a subset of mdDA neurons. (C) Combined ISH (purple) and immunohistochemistry (brown) experiment using Chrna6 and Chrnb3 probes with Th antibodies confirm the co-localization and restriction to the mdDA neuronal pool of the Chrna6 and Chrnb3 transcripts. L, lateral; M, medial. Koushik Chakrabarty et al. Biology Open 2012;1:693-704 © 2012. Published by The Company of Biologists Ltd