| human | Q5 |
| P2798 | Loop ID | 4390 |
| P496 | ORCID iD | 0000-0001-8781-7846 |
| P1153 | Scopus author ID | 7006021457 |
| P69 | educated at | Cornell University | Q49115 |
| Albert Einstein College of Medicine | Q2030894 | ||
| P108 | employer | Albert Einstein College of Medicine | Q2030894 |
| Columbia University Vagelos College of Physicians and Surgeons | Q2154182 | ||
| P735 | given name | Myles | Q20635317 |
| Myles | Q20635317 | ||
| P106 | occupation | researcher | Q1650915 |
| P21 | sex or gender | male | Q6581097 |
| Q35238474 | 5-HT3 receptor ion size selectivity is a property of the transmembrane channel, not the cytoplasmic vestibule portals. |
| Q43892118 | A bitter substance induces a rise in intracellular calcium in a subpopulation of rat taste cells |
| Q88184481 | A closer look at attrition in MD-PhD programs |
| Q40362619 | A role for the beta 1-beta 2 loop in the gating of 5-HT3 receptors. |
| Q90437338 | Accessibility of substituted cysteines in TM2 and TM10 transmembrane segments in the Plasmodium falciparum equilibrative nucleoside transporter PfENT1 |
| Q34250941 | Acetylcholine receptor channel structure probed in cysteine-substitution mutants. |
| Q35636848 | Are MD-PhD programs meeting their goals? An analysis of career choices made by graduates of 24 MD-PhD programs. |
| Q77374642 | Arg352 is a major determinant of charge selectivity in the cystic fibrosis transmembrane conductance regulator chloride channel |
| Q24616479 | Balance of activity between LN(v)s and glutamatergic dorsal clock neurons promotes robust circadian rhythms in Drosophila |
| Q24683541 | Channel opening by anesthetics and GABA induces similar changes in the GABAA receptor M2 segment |
| Q48933240 | Channel-lining residues in the M3 membrane-spanning segment of the cystic fibrosis transmembrane conductance regulator |
| Q30357176 | Chloroquine-resistant isoforms of the Plasmodium falciparum chloroquine resistance transporter acidify lysosomal pH in HEK293 cells more than chloroquine-sensitive isoforms. |
| Q38588680 | Cysteine Modification: Probing Channel Structure, Function and Conformational Change. |
| Q44727242 | Defining the propofol binding site location on the GABAA receptor |
| Q45136832 | Differential protein mobility of the gamma-aminobutyric acid, type A, receptor alpha and beta subunit channel-lining segments |
| Q36242467 | Emerging molecular mechanisms of general anesthetic action. |
| Q41817367 | Erythrocytic adenosine monophosphate as an alternative purine source in Plasmodium falciparum. |
| Q43757149 | Evidence for distinct conformations of the two alpha 1 subunits in diazepam-bound GABA(A) receptors |
| Q45136842 | Functional and structural analysis of the GABAA receptor alpha 1 subunit during channel gating and alcohol modulation |
| Q44133863 | GABA(A) receptor M2-M3 loop secondary structure and changes in accessibility during channel gating. |
| Q34365717 | GABAA receptor structure-function studies: a reexamination in light of new acetylcholine receptor structures |
| Q34171714 | Gamma-aminobutyric acid increases the water accessibility of M3 membrane-spanning segment residues in gamma-aminobutyric acid type A receptors |
| Q36201884 | Gating-induced conformational rearrangement of the γ-aminobutyric acid type A receptor β-α subunit interface in the membrane-spanning domain |
| Q49036560 | Identification of acetylcholine receptor channel-lining residues in the M1 segment of the alpha-subunit |
| Q49088255 | Identification of acetylcholine receptor channel-lining residues in the entire M2 segment of the alpha subunit |
| Q24320048 | Identification of an intestinal folate transporter and the molecular basis for hereditary folate malabsorption |
| Q34017913 | Identification of cystic fibrosis transmembrane conductance regulator channel-lining residues in and flanking the M6 membrane-spanning segment. |
| Q68453698 | Identification of electrophysiologically distinct subpopulations of rat taste cells |
| Q92362125 | Identification via a Parallel Hit Progression Strategy of Improved Small Molecule Inhibitors of the Malaria Purine Uptake Transporter that Inhibit Plasmodium falciparum Parasite Proliferation |
| Q92246170 | Impact of Field Isolate Identified Nonsynonymous Single Nucleotide Polymorphisms on Plasmodium falciparum Equilibrative Nucleoside Transporter 1 Inhibitor Efficacy |
| Q34047528 | Interaction of picrotoxin with GABAA receptor channel-lining residues probed in cysteine mutants. |
| Q31060057 | Length and amino acid sequence of peptides substituted for the 5-HT3A receptor M3M4 loop may affect channel expression and desensitization |
| Q36411911 | Locating the anion-selectivity filter of the cystic fibrosis transmembrane conductance regulator (CFTR) chloride channel. |
| Q90553121 | MD-PhD graduates remain underrepresented in orthopaedic surgery: National MD-PhD Program Outcome Survey update |
| Q27974769 | Malaria parasite type 4 equilibrative nucleoside transporters (ENT4) are purine transporters with distinct substrate specificity |
| Q44949009 | Na+/Ca2+ exchange inhibitors: potential drugs to mitigate the severity of ischemic injury |
| Q72934239 | Osmotic swelling of phospholipid vesicles causes them to fuse with a planar phospholipid bilayer membrane |
| Q27861959 | Probing the multifactorial basis of Plasmodium falciparum quinine resistance: Evidence for a strain-specific contribution of the sodium-proton exchanger PfNHE |
| Q41725516 | Probing the structural and functional domains of the CFTR chloride channel. |
| Q69077037 | Purification and reconstitution of chloride channels from kidney and trachea |
| Q67684177 | Purification and reconstitution of epithelial chloride channels |
| Q41823215 | Purification of the Epithelial Cl Channel |
| Q35513431 | Purine import into malaria parasites as a target for antimalarial drug development |
| Q34693868 | Rodent intestinal folate transporters (SLC46A1): secondary structure, functional properties, and response to dietary folate restriction. |
| Q46642853 | Spontaneous thermal motion of the GABA(A) receptor M2 channel-lining segments. |
| Q42684049 | State-dependent cross-linking of the M2 and M3 segments: functional basis for the alignment of GABAA and acetylcholine receptor M3 segments. |
| Q42659707 | Structural and electrostatic properties of the 5-HT3 receptor pore revealed by substituted cysteine accessibility mutagenesis. |
| Q34800089 | Structure of the M2 transmembrane segment of GLIC, a prokaryotic Cys loop receptor homologue from Gloeobacter violaceus, probed by substituted cysteine accessibility. |
| Q77121562 | Substituted-cysteine accessibility method |
| Q36947737 | Substrate and Inhibitor Specificity of the Plasmodium berghei Equilibrative Nucleoside Transporter Type 1 |
| Q43623297 | Taking Charge: Feeding Malaria via Anion Channels |
| Q36446094 | Targeting the Plasmodium vivax equilibrative nucleoside transporter 1 (PvENT1) for antimalarial drug development |
| Q36299672 | The location of a closed channel gate in the GABAA receptor channel. |
| Q90440708 | The national MD-PhD program outcomes study: Outcomes variation by sex, race, and ethnicity |
| Q90440749 | The national MD-PhD program outcomes study: Relationships between medical specialty, training duration, research effort, and career paths |
| Q41142209 | Toward a structural basis for the function of nicotinic acetylcholine receptors and their cousins. |
| Q37439211 | Transport of purines and purine salvage pathway inhibitors by the Plasmodium falciparum equilibrative nucleoside transporter PfENT1. |
| Q37311917 | UV-triggered affinity capture identifies interactions between the Plasmodium falciparum multidrug resistance protein 1 (PfMDR1) and antimalarial agents in live parasitized cells |
| Q37240694 | Using molecular dynamics to elucidate the structural basis for function in pLGICs |
| Q82584214 | Watching single protons bind |
| Q35545065 | Yeast-based high-throughput screen identifies Plasmodium falciparum equilibrative nucleoside transporter 1 inhibitors that kill malaria parasites |
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