Connection

CECILIA LJUNGBERG to Animals

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

0.244
  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: 0.020
  2. Rapamycin suppresses seizures and neuronal hypertrophy in a mouse model of cortical dysplasia. Dis Model Mech. 2009 Jul-Aug; 2(7-8):389-98.
    View in: PubMed
    Score: 0.017
  3. 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: 0.015
  4. Semaphorin 3E-Plexin-D1 Pathway Downstream of the Luteinizing Hormone Surge Regulates Ovulation, Granulosa Cell Luteinization, and Ovarian Angiogenesis in Mice. Adv Sci (Weinh). 2025 Aug; 12(29):e17163.
    View in: PubMed
    Score: 0.013
  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: 0.013
  6. A comprehensive atlas of AAV tropism in the mouse. Mol Ther. 2025 Mar 05; 33(3):1282-1299.
    View in: PubMed
    Score: 0.013
  7. Molecular logic for cellular specializations that initiate the auditory parallel processing pathways. Nat Commun. 2025 Jan 09; 16(1):489.
    View in: PubMed
    Score: 0.013
  8. A single-cell transcriptomic map of the developing Atoh1 lineage identifies neural fate decisions and neuronal diversity in the hindbrain. Dev Cell. 2024 08 19; 59(16):2171-2188.e7.
    View in: PubMed
    Score: 0.012
  9. An oocyte-specific Cas9-expressing mouse for germline CRISPR/Cas9-mediated genome editing. Genesis. 2024 04; 62(2):e23589.
    View in: PubMed
    Score: 0.012
  10. Targeting AAV vectors to the central nervous system by engineering capsid-receptor interactions that enable crossing of the blood-brain barrier. PLoS Biol. 2023 07; 21(7):e3002112.
    View in: PubMed
    Score: 0.011
  11. SOX7 deficiency causes ventricular septal defects through its effects on endocardial-to-mesenchymal transition and the expression of Wnt4 and Bmp2. Hum Mol Genet. 2023 06 19; 32(13):2152-2161.
    View in: PubMed
    Score: 0.011
  12. 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: 0.011
  13. In vivo editing of the pan-endothelium by immunity evading simian adenoviral vector. Biomed Pharmacother. 2023 Feb; 158:114189.
    View in: PubMed
    Score: 0.011
  14. Truncated apoE forms tangle-like structures in a neuronal cell line. Neuroreport. 2002 May 07; 13(6):867-70.
    View in: PubMed
    Score: 0.011
  15. 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: 0.009
  16. VCAM1 Is Induced in Ovarian Theca and Stromal Cells in a Mouse Model of Androgen Excess. Endocrinology. 2019 06 01; 160(6):1377-1393.
    View in: PubMed
    Score: 0.009
  17. The neurotrophins NGF and NT-3 reduce sensory neuronal loss in adult rat after peripheral nerve lesion. Neurosci Lett. 1999 Feb 26; 262(1):29-32.
    View in: PubMed
    Score: 0.008
  18. Survival of genetically engineered, adult-derived rat astrocytes grafted into the 6-hydroxydopamine lesioned adult rat striatum. Brain Res. 1999 Jan 16; 816(1):29-37.
    View in: PubMed
    Score: 0.008
  19. 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: 0.007
  20. 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: 0.007
  21. 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: 0.005
  22. 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: 0.004
  23. Apolipoprotein E gene and Alzheimer's disease: is tau the link? Biochem Soc Symp. 2001; (67):111-20.
    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.