L
Lily Yeh Jan
Researcher at University of California, San Francisco
Publications - 476
Citations - 77737
Lily Yeh Jan is an academic researcher from University of California, San Francisco. The author has contributed to research in topics: Potassium channel & Inward-rectifier potassium ion channel. The author has an hindex of 162, co-authored 467 publications receiving 73655 citations. Previous affiliations of Lily Yeh Jan include University of California & Sandia National Laboratories.
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Interactions between heterologous helix-loop-helix proteins generate complexes that bind specifically to a common DNA sequence.
Cornelis Murre,Patrick S. McCaw,H. Vaessin,M. Caudy,Lily Yeh Jan,Yuh Nung Jan,Carlos V. Cabrera,Jean N. Buskin,Stephen D. Hauschka,Andrew B. Lassar,Harold Weintraub,David Baltimore +11 more
TL;DR: The HLH domain can mediate heterodimer formation between either daughterless, E12, or E47 and achaete-scute T3 or MyoD to form proteins with high affinity for the kappa E2 site in the immunoglobulin kappa chain enhancer.
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Synaptic vesicle exocytosis captured by quick freezing and correlated with quantal transmitter release.
TL;DR: The utility of quick- freezing as a technique to capture biological processes as evanescent as synaptic transmission as well as physiological demonstrations that quanta are discharged independently has been established.
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Changing subunit composition of heteromeric NMDA receptors during development of rat cortex
TL;DR: Direct evidence is presented that NMDA receptors exist in rat neocortex as heteromeric complexes of considerable heterogeneity, some containing both NR2A and NR2B subunits.
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A new ER trafficking signal regulates the subunit stoichiometry of plasma membrane K(ATP) channels.
TL;DR: It is concluded that exposure of a three amino acid motif (RKR) can explain how assembly of an ion channel complex is coupled to intracellular trafficking.
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Expression cloning of TMEM16A as a calcium-activated chloride channel subunit.
TL;DR: Using Axolotl oocytes as an expression system, TMEM16A is identified as the Xenopus oocyte CaCC and may help the development of CaCC modulators for treating diseases including hypertension and cystic fibrosis.