Srinivas B. Narayan

发表

Reproducibility and quantification of illicit drugs using matrix-assisted ionization (MAI) mass spectrometry.

S. Trimpin, Daniel W. Woodall, Kevin Jooss, 2015, Analytical chemistry.

Bile acylcarnitine profiles in pediatric liver disease do not interfere with the diagnosis of long-chain fatty acid oxidation defects.

M. Bennett, Robert H. Squires, Srinivas B. Narayan, 2006, Clinica chimica acta; international journal of clinical chemistry.

Juvenile neuronal ceroid-lipofuscinosis (Batten disease): a brief review and update.

D. Rakheja, M. Bennett, Srinivas B. Narayan, 2007, Current molecular medicine.

CLN3P, the Batten's disease protein, is a novel palmitoyl‐protein Δ‐9 desaturase

D. Rakheja, M. Bennett, J. Pastor, 2006 .

Intermediate levels of neuronal palmitoyl-protein Delta-9 desaturase in heterozygotes for murine Batten disease.

M. Bennett, Srinivas B. Narayan, Lu Tan, 2008, Molecular genetics and metabolism.

The function of CLN3P, the Batten disease protein.

D. Rakheja, M. Bennett, Srinivas B. Narayan, 2008, Molecular genetics and metabolism.

CLN3P, the Batten disease protein, localizes to membrane lipid rafts (detergent-resistant membranes).

D. Rakheja, M. Bennett, J. Pastor, 2004, Biochemical and biophysical research communications.

Over-expression of CLN3P, the Batten disease protein, inhibits PANDER-induced apoptosis in neuroblastoma cells: further evidence that CLN3P has anti-apoptotic properties.

B. Wolf, K. Rosenblatt, D. Rakheja, 2006, Molecular genetics and metabolism.

CLN3L, a novel protein related to the Batten disease protein, is overexpressed in Cln3-/- mice and in Batten disease.

M. Bennett, H. Mitchison, J. Pastor, 2004, Brain : a journal of neurology.

Screening for calcium channel modulators in CLN3 siRNA knock down SH-SY5Y neuroblastoma cells reveals a significant decrease of intracellular calcium levels by selected L-type calcium channel blockers.

M. Bennett, Srinivas B. Narayan, K. an Haack, 2011, Biochimica et biophysica acta.

CLN3P, the Batten's disease protein, is a novel palmitoyl-protein Delta-9 desaturase.

D. Rakheja, M. Bennett, J. Pastor, 2006, Annals of neurology.

A rapid ultra performance liquid chromatography tandem mass spectrometric method for measuring amino acids associated with maple syrup urine disease, tyrosinaemia and phenylketonuria

M. Bennett, Jie Chen, Donald S. Mason, 2007, Annals of clinical biochemistry.

Flow injection tandem mass spectrometric measurement of ceramides of multiple chain lengths in biological samples.

M. Bennett, Jie Chen, A. Edinger, 2012, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

PTC124 improves readthrough and increases enzymatic activity of the CPT1A R160X nonsense mutation

M. Bennett, Jie Chen, Srinivas B. Narayan, 2011, Journal of Inherited Metabolic Disease.

New Ionization Processes for Ionizing Nonvolatile Compounds in Mass Spectrometry: The Road of Discovery to Current State-of-the-Art

Scott M. Grayson, V. Shulaev, T. Sanderson, 2020 .

Matrix-Assisted Ionization on a Portable Mass Spectrometer: Analysis Directly from Biological and Synthetic Materials.

Joshua L. Fischer, S. Trimpin, C. Reynolds, 2016, Analytical chemistry.

Seizures and vertigo in a young infant

P. Jones, M. Bennett, Srinivas B. Narayan, 2003 .

case studies: Seizures and Vertigo in a Young Infant

P. Jones, M. Bennett, Srinivas B. Narayan, 2003 .

Novel mutations in CPT 1A define molecular heterogeneity of hepatic carnitine palmitoyltransferase I deficiency.

M. Bennett, R. Boriack, M. Raff, 2004, Molecular genetics and metabolism.

Reye-like syndrome resulting from novel missense mutations in mitochondrial medium- and short-chain l-3-hydroxy-acyl-CoA dehydrogenase.

M. Bennett, R. Boriack, A. Strauss, 2006, Molecular genetics and metabolism.

Amlodipine prevents apoptotic cell death by correction of elevated intracellular calcium in a primary neuronal model of Batten disease (CLN3 disease).

M. Bennett, Changhong Li, Srinivas B. Narayan, 2013, Biochemical and biophysical research communications.

The potential for clinical applications using a new ionization method combined with ion mobility spectrometry-mass spectrometry

S. Trimpin, Srinivas B. Narayan, J. Wager-Miller, 2013, International Journal for Ion Mobility Spectrometry.

Mechanism of Hyperinsulinism in Short-chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency Involves Activation of Glutamate Dehydrogenase*

C. Stanley, T. Smith, H. Collins, 2010, The Journal of Biological Chemistry.

Green Tea Polyphenols Control Dysregulated Glutamate Dehydrogenase in Transgenic Mice by Hijacking the ADP Activation Site*

Changhong Li, Thomas J Smith, C. Stanley, 2011, The Journal of Biological Chemistry.

Establishing a reference interval for measurement of flux through the mitochondrial fatty acid oxidation pathway in cultured skin fibroblasts.

M. Bennett, R. Boriack, Srinivas B. Narayan, 2005, Clinical chemistry.

False-positive cannabinoid screens in adult cystic fibrosis patients treated with lumacaftor/ivacaftor.

G. Marigowda, C. Simard, Srinivas B. Narayan, 2018, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Measurement of plasma amino acids by Ultraperformance® Liquid Chromatography

M. Bennett, Srinivas B. Narayan, Kendon S. Graham, 2011, Clinical chemistry and laboratory medicine.

Short-Chain 3-Hydroxyacyl-Coenzyme A Dehydrogenase Associates with a Protein Super-Complex Integrating Multiple Metabolic Pathways

C. Stanley, S. Master, M. Bennett, 2012, PloS one.

Diagnosis of a patient with a kinetic variant of medium and short-chain 3-hydroxyacyl-CoA dehydrogenase deficiency by newborn screening.

L. Vilarinho, M. Bennett, Srinivas B. Narayan, 2012, Molecular genetics and metabolism.

High-throughput characterization of small and large molecules using only a matrix and the vacuum of a mass spectrometer.

S. Trimpin, Daniel W. Woodall, Beixi Wang, 2015, Analytical chemistry.

Measurement of β1- and β2-Globulins Improves Detection of M-Spikes on High-Resolution Electrophoresis

S. Devaraj, I. Jialal, C. Rutherford, 2003 .

Molecular assay for detection of the common carnitine palmitoyltransferase 1A 1436(C>T) mutation

Jason Y. Park, M. Bennett, Srinivas B. Narayan, 2006, Clinical Chemistry and Laboratory Medicine.

Reproducibility and quantification of illicit drugs using matrix-assisted ionization (MAI) mass spectrometry.

S. Trimpin, Daniel W. Woodall, Kevin Jooss, 2015, Analytical chemistry.