Searching across hundreds of databases

Our searching services are busy right now. Your search will reload in five seconds.

X
Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.

X
Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.

Laser-capture microdissection and transcriptional profiling of the dorsomedial nucleus of the hypothalamus.

The Journal of comparative neurology | 2012

Identifying neuronal molecular markers with restricted patterns of expression is a crucial step in dissecting the numerous pathways and functions of the brain. While the dorsomedial nucleus of the hypothalamus (DMH) has been implicated in a host of physiological processes, current functional studies have been limited by the lack of molecular markers specific for DMH. Identification of such markers would facilitate the development of mouse models with DMH-specific genetic manipulations. Here we used a combination of laser-capture microdissection (LCM) and gene expression profiling to identify genes that are highly expressed within the DMH relative to adjacent hypothalamic regions. Six of the most highly expressed of these genes, Gpr50, 4930511J11Rik, Pcsk5, Grp, Sulf1, and RorĪ², were further characterized by real-time polymerase chain reaction (PCR) analysis and in situ hybridization histochemistry. The genes identified in this article will provide the basis for future gene-targeted approaches for studying DMH function.

Pubmed ID: 22473294 RIS Download

Research resources used in this publication

Additional research tools detected in this publication

Antibodies used in this publication

Associated grants

  • Agency: NIDDK NIH HHS, United States
    Id: P01 DK088761
  • Agency: NICHD NIH HHS, United States
    Id: R01 HD061539
  • Agency: NIDDK NIH HHS, United States
    Id: RL1 DK081185
  • Agency: NIDDK NIH HHS, United States
    Id: R37 DK053301
  • Agency: NIDDK NIH HHS, United States
    Id: RL1DK081185
  • Agency: NIDDK NIH HHS, United States
    Id: R01 DK053301
  • Agency: NIDDK NIH HHS, United States
    Id: R01 DK53301
  • Agency: NCRR NIH HHS, United States
    Id: UL1 RR024923
  • Agency: NIDDK NIH HHS, United States
    Id: PL1 DK081182

Publication data is provided by the National Library of Medicine ® and PubMed ®. Data is retrieved from PubMed ® on a weekly schedule. For terms and conditions see the National Library of Medicine Terms and Conditions.

This is a list of tools and resources that we have found mentioned in this publication.


AxioVision Imaging System (tool)

RRID:SCR_002677

Digital image processing system where microscope settings and processing steps may be adjusted in single user interface. Can acquire images from variety of cameras. Includes software package for capturing, archiving and preparing images for publication. Allows users to visualize and present images in several dimensions. Functionality of imaging toolbox expands constantly with wide range of different modules that are tailored to specific applications or microscope accessories. This resource is duplicated by SCR_018376

View all literature mentions

Phospho-Stat-3 (tyr705) (antibody)

RRID:AB_331586

This polyclonal targets Phospho-Stat3 (Tyr705) Antibody detects endogenous levels of Stat3 only when phosphorylated at Tyr705. The antibody does not cross-react with other Stat proteins when phosphorylated on the corresponding tyrosine residue. Does cross-react withPhospho-EGFR

View all literature mentions

Phospho-Stat-3 (tyr705) (antibody)

RRID:AB_331586

This polyclonal targets Phospho-Stat3 (Tyr705) Antibody detects endogenous levels of Stat3 only when phosphorylated at Tyr705. The antibody does not cross-react with other Stat proteins when phosphorylated on the corresponding tyrosine residue. Does cross-react withPhospho-EGFR

View all literature mentions