Associate Professor, Medicine, UCSD School of Medicine

Internal Medicine

Satish A. Eraly, MD practices Internal Medicine. He went to University of California San Diego School of Medicine. University of California San Diego School of Medicine is ranked 17/19 in Research/PrimaryCare. Dr. Satish A. Eraly is a published doctor and has 35 publications published. The lastest was: 'The GnRH promoter: target of transcription factors, hormones, and signaling pathways.'

Publications

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• Assessment of Plasma C-Reactive Protein as a Biomarker of Posttraumatic Stress Disorder Risk.
• Multispecific Drug Transporter Oat3 (Slc22a8) Regulates Multiple Metabolic Pathways.
• Organic anion transport pathways in antiviral handling in choroid plexus in Oat1 (Slc22a6) and Oat3 (Slc22a8) deficient tissue.
• Syndrome of inappropriate antidiuretic hormone associated with moxifloxacin.
• Linkage of organic anion transporter-1 to metabolic pathways through integrated omics-driven network and functional analysis.
• Analysis of three-dimensional systems for developing and mature kidneys clarifies the role of OAT1 and OAT3 in antiviral handling.
• Interaction of organic cations with organic anion transporters.
• Analysis of a large cluster of SLC22 transporter genes, including novel USTs, reveals species-specific amplification of subsets of family members.
• Implications of the alternating access model for organic anion transporter kinetics.
• Organic anion transporter 3 contributes to the regulation of blood pressure.
• Multiple organic anion transporters contribute to net renal excretion of uric acid.
• Overlapping in vitro and in vivo specificities of the organic anion transporters OAT1 and OAT3 for loop and thiazide diuretics.
• Structural variation governs substrate specificity for organic anion transporter (OAT) homologs. Potential remote sensing by OAT family members.
• Olfactory mucosa-expressed organic anion transporter, Oat6, manifests high affinity interactions with odorant organic anions.
• Decreased renal organic anion secretion and plasma accumulation of endogenous organic anions in OAT1 knock-out mice.
• Analyses of coding region polymorphisms in apical and basolateral human organic anion transporter (OAT) genes [OAT1 (NKT), OAT2, OAT3, OAT4, URAT (RST)].
• Identification of a novel murine organic anion transporter family member, OAT6, expressed in olfactory mucosa.
• Novel slc22 transporter homologs in fly, worm, and human clarify the phylogeny of organic anion and cation transporters.
• The molecular pharmacology of organic anion transporters: from DNA to FDA?
• Debt91, a putative zinc finger protein differentially expressed during epithelial morphogenesis.
• Organic anion and cation transporters occur in pairs of similar and similarly expressed genes.
• Novel human cDNAs homologous to Drosophila Orct and mammalian carnitine transporters.
• Organic anion transporter 3 inhibitors as potential novel antihypertensives.
• Organic anion and cation transporter expression and function during embryonic kidney development and in organ culture models.
• Analyses of 5'' regulatory region polymorphisms in human SLC22A6 (OAT1) and SLC22A8 (OAT3).
• Novel aspects of renal organic anion transporters.
• Immortalized hypothalamic gonadotropin-releasing hormone neurons.
• Regulation of gonadotropin-releasing hormone transcription by protein kinase C is mediated by evolutionarily conserved promoter-proximal elements.
• A neuron-specific enhancer targets expression of the gonadotropin-releasing hormone gene to hypothalamic neurosecretory neurons.
• Hypothalamus-specific regulation of gonadotropin-releasing hormone gene expression.
• Regulation of gonadotropin-releasing hormone by protein kinase-A and -C in immortalized hypothalamic neurons.
• Oct-1 binds promoter elements required for transcription of the GnRH gene.
• The GnRH promoter: target of transcription factors, hormones, and signaling pathways.
• Striking Differences between Knockout and Wild-Type Mice in Global Gene Expression Variability.

Schools

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• University of California At San Diego

Doctors Specialties

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• Internal Medicine

Accepted Insurances

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Education

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• University of California San Diego
• University of California San Diego School of Medicine

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