Laura Bauer Callaway LPC ATR BC
Counselor/Therapist
25 W FAYETTE ST UNIONTOWN PA, 15401About
Laura Callaway is a counselor in UNIONTOWN, PA. Laura evaluates patients using many different procedures, in order to determine what treatments must be carried out in order to properly assess their symptoms. Counselors provide consultation for each patient and their families.
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Expert Publications
Data provided by the National Library of Medicine- Discovery and SAR of 4-amino-2-biarylbutylurea MCH 1 receptor antagonists through solid-phase parallel synthesis.
- Discovery and SAR of biaryl piperidine MCH1 receptor antagonists through solid-phase encoded combinatorial synthesis.
- Surfing the piperazine core of tricyclic farnesyltransferase inhibitors.
- Guiding farnesyltransferase inhibitors from an ECLiPS library to the catalytic zinc.
- Synthesis and structure-activity relationships of 3,4-diaminocyclobut-3-ene-1,2-dione CXCR2 antagonists.
- Exploring structure-activity relationships of tricyclic farnesyltransferase inhibitors using ECLiPS libraries.
- Biological examination of melanin concentrating hormone receptor 1: multi-tasking from the hypothalamus.
- Biological examination of melanin concentrating hormone receptor 1: multi-tasking from the hypothalamus.
- Discovery of 2-hydroxy-N,N-dimethyl-3-{2-[[(R)-1-(5- methylfuran-2-yl)propyl]amino]-3,4-dioxocyclobut-1-enylamino}benzamide (SCH 527123): a potent, orally bioavailable CXCR2/CXCR1 receptor antagonist.
- Discovery and preliminary evaluation of 5-(4-phenylbenzyl)oxazole-4-carboxamides as prostacyclin receptor antagonists.
- Discovery of tetralin ureas as potent melanin concentrating hormone 1 receptor antagonists.
- Design, synthesis, and evaluation of tetrahydroquinoline and pyrrolidine sulfonamide carbamates as gamma-secretase inhibitors.
- Synthesis and structure-activity relationships of new disubstituted phenyl-containing 3,4-diamino-3-cyclobutene-1,2-diones as CXCR2 receptor antagonists.
- Synthesis of 2-amino-5-benzoyl-4-(2-furyl)thiazoles as adenosine A(2A) receptor antagonists.
- Synthesis and SAR studies of trisubstituted purinones as potent and selective adenosine A2A receptor antagonists.
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