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Connection

Luca Maragliano to Humans

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

0.182
  1. Computational study of ion permeation through claudin-4 paracellular channels. Ann N Y Acad Sci. 2022 10; 1516(1):162-174.
    View in: PubMed
    Score: 0.027
  2. Structural Mechanism of ?-Currents in a Mutated Kv7.2 Voltage Sensor Domain from Molecular Dynamics Simulations. J Chem Inf Model. 2021 03 22; 61(3):1354-1367.
    View in: PubMed
    Score: 0.025
  3. Thermodynamics and Kinetics of Ion Permeation in Wild-Type and Mutated Open Active Conformation of the Human a7 Nicotinic Receptor. J Chem Inf Model. 2020 10 26; 60(10):5045-5056.
    View in: PubMed
    Score: 0.024
  4. A refined model of claudin-15 tight junction paracellular architecture by molecular dynamics simulations. PLoS One. 2017; 12(9):e0184190.
    View in: PubMed
    Score: 0.019
  5. A possible desensitized state conformation of the human a7 nicotinic receptor: A molecular dynamics study. Biophys Chem. 2017 10; 229:99-109.
    View in: PubMed
    Score: 0.019
  6. Constitutive opening of the Kv7.2 pore activation gate causes KCNQ2-developmental encephalopathy. Proc Natl Acad Sci U S A. 2024 Dec 03; 121(49):e2412388121.
    View in: PubMed
    Score: 0.008
  7. Unraveling the Membrane Topology of TMEM151A: A Step Towards Understanding its Cellular Role. J Mol Biol. 2024 Dec 01; 436(23):168834.
    View in: PubMed
    Score: 0.008
  8. Molecular Dynamics Simulations of Ion Permeation in Human Voltage-Gated Sodium Channels. J Chem Theory Comput. 2023 May 23; 19(10):2953-2972.
    View in: PubMed
    Score: 0.007
  9. The intramembrane COOH-terminal domain of PRRT2 regulates voltage-dependent Na+ channels. J Biol Chem. 2023 05; 299(5):104632.
    View in: PubMed
    Score: 0.007
  10. Phenotypic and genetic spectrum of ATP6V1A encephalopathy: a disorder of lysosomal homeostasis. Brain. 2022 08 27; 145(8):2687-2703.
    View in: PubMed
    Score: 0.007
  11. Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations. J Clin Immunol. 2021 05; 41(4):756-768.
    View in: PubMed
    Score: 0.006
  12. Engineering REST-Specific Synthetic PUF Proteins to Control Neuronal Gene Expression: A Combined Experimental and Computational Study. ACS Synth Biol. 2020 08 21; 9(8):2039-2054.
    View in: PubMed
    Score: 0.006
  13. Closed-Locked and Apo-Resting State Structures of the Human a7 Nicotinic Receptor: A Computational Study. J Chem Inf Model. 2018 11 26; 58(11):2278-2293.
    View in: PubMed
    Score: 0.005
  14. De novo mutations of the ATP6V1A gene cause developmental encephalopathy with epilepsy. Brain. 2018 06 01; 141(6):1703-1718.
    View in: PubMed
    Score: 0.005
  15. A Structural Model of the Human a7 Nicotinic Receptor in an Open Conformation. PLoS One. 2015; 10(7):e0133011.
    View in: PubMed
    Score: 0.004
  16. Behavioural and physiological indicators of shelter dogs' welfare: reflections on the no-kill policy on free-ranging dogs in Italy revisited on the basis of 15 years of implementation. Physiol Behav. 2014 Jun 22; 133:223-9.
    View in: PubMed
    Score: 0.004
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.