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Blackshaw Lab

Building and Rebuilding the Retina and Hypothalamus

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Category: <span>Diabetes</span>

Diabetic gastropathy in mice reflects loss of neuronal nitric oxide synthase that is restored by insulin

Diabetes, Neurotransmitters, Nitric oxide, Signal transduction

Watkins CC, Sawa A, Jaffrey SR, Blackshaw S, Barrow RK, Ferris CD, Snyder SH. J Clin Invest 2000 106:373-384

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PARP-deficient mice are resistant to streptozoocin-induced diabetes

Diabetes, Metabolism

Pieper AA, Brat D, Krug D, Watkins C, Blackshaw S, Gupta A, Verma A, Snyder SH. Proc Natl Acad Sci USA 1999 96:3059-64.

Link to Article>> View PDF>>

Research Areas

  • AAV
  • Antibody specificity
  • ATAC-Seq
  • Autoimmune disease
  • Behavior
  • Book Chapter
  • Cell fate
  • Cell lineage analysis
  • Chemical senses
  • Chemogenetics
  • ChIP-Seq
  • Circadian
  • Commentary
  • D-Amino acids
  • Development
  • Diabetes
  • Extraretinal photoreceptors
  • FGF
  • Human genetics
  • Hypothalamus
  • In vivo electroporation
  • Lens
  • Lhx2
  • lncRNAs
  • Metabolism
  • Muller glia
  • Neural circuitry
  • Neural development
  • Neurodegeneration
  • Neurogenesis
  • Neurotransmitters
  • New technique
  • Nitric oxide
  • Notch/Delta
  • Nucleogenesis
  • Photoreceptor
  • Protein microarray
  • Proteomics
  • Protocol
  • Radial glia
  • Retina
  • Review article
  • RNA binding proteins
  • RNA splicing
  • RPE
  • SAGE
  • scRNA-Seq
  • Shh
  • Signal transduction
  • Sleep
  • Spatial patterning
  • SUMOylation
  • Suprachiasmatic nucleus
  • Tanycytes
  • Thalamus
  • Transcription factor
  • Transcriptomics
  • Visual cycle
  • Wnt

Recent Posts

  • Cell-specific regulation of gene expression using splicing-dependent frameshifting
  • Ectopic insert-dependent neuronal expression of GFAP promoter-driven AAV constructs in adult mouse retina
  • LRLoop: A method to predict feedback loops in cell-cell communication
  • Notch Inhibition Promotes Regeneration and Immunosuppression Supports Cone Survival in a Zebrafish Model of Inherited Retinal Dystrophy
  • Genetic loss of function of Ptbp1 does not induce glia-to-neuron conversion in retina

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