Connection

CECILIA LJUNGBERG to Humans

This is a "connection" page, showing publications CECILIA LJUNGBERG has written about Humans.
Connection Strength

0.068
  1. CREB-activity and nmnat2 transcription are down-regulated prior to neurodegeneration, while NMNAT2 over-expression is neuroprotective, in a mouse model of human tauopathy. Hum Mol Genet. 2012 Jan 15; 21(2):251-67.
    View in: PubMed
    Score: 0.010
  2. LungMAP: The Molecular Atlas of Lung Development Program. Am J Physiol Lung Cell Mol Physiol. 2017 Nov 01; 313(5):L733-L740.
    View in: PubMed
    Score: 0.007
  3. Activation of mammalian target of rapamycin in cytomegalic neurons of human cortical dysplasia. Ann Neurol. 2006 Oct; 60(4):420-9.
    View in: PubMed
    Score: 0.007
  4. Cell Population-resolved Multiomics Atlas of the Developing Lung. Am J Respir Cell Mol Biol. 2025 May; 72(5):484-495.
    View in: PubMed
    Score: 0.006
  5. In vivo expansion of gene-targeted hepatocytes through transient inhibition of an essential gene. Sci Transl Med. 2025 Feb 12; 17(785):eadk3920.
    View in: PubMed
    Score: 0.006
  6. A comprehensive atlas of AAV tropism in the mouse. Mol Ther. 2025 Mar 05; 33(3):1282-1299.
    View in: PubMed
    Score: 0.006
  7. Apolipoprotein E (apoE) uptake and distribution in mammalian cell lines is dependent upon source of apoE and can be monitored in living cells. Neurosci Lett. 2003 Apr 24; 341(1):69-73.
    View in: PubMed
    Score: 0.005
  8. S100a4-Cre-mediated deletion of Patched1 causes hypogonadotropic hypogonadism: role of pituitary hematopoietic cells in endocrine regulation. JCI Insight. 2019 07 02; 5.
    View in: PubMed
    Score: 0.004
  9. Multifunctional Activity-Based Protein Profiling of the Developing Lung. J Proteome Res. 2018 08 03; 17(8):2623-2634.
    View in: PubMed
    Score: 0.004
  10. Biallelic Variants in OTUD6B Cause an Intellectual Disability Syndrome Associated with Seizures and Dysmorphic Features. Am J Hum Genet. 2017 Apr 06; 100(4):676-688.
    View in: PubMed
    Score: 0.004
  11. Disruption of the ATXN1-CIC complex causes a spectrum of neurobehavioral phenotypes in mice and humans. Nat Genet. 2017 Apr; 49(4):527-536.
    View in: PubMed
    Score: 0.004
  12. Deletion of Porcn in mice leads to multiple developmental defects and models human focal dermal hypoplasia (Goltz syndrome). PLoS One. 2012; 7(3):e32331.
    View in: PubMed
    Score: 0.003
  13. A neuronal VLDLR variant lacking the third complement-type repeat exhibits high capacity binding of apoE containing lipoproteins. Brain Res. 2009 Jun 18; 1276:11-21.
    View in: PubMed
    Score: 0.002
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.