C. Macmullen

发表

Expression, purification and characterization of human glutamate dehydrogenase (GDH) allosteric regulatory mutations.

C. Stanley, T. Smith, Jie Fang, 2002, The Biochemical journal.

A Novel KCNJ11 Mutation Associated with Congenital Hyperinsulinism Reduces the Intrinsic Open Probability of β-Cell ATP-sensitive Potassium Channels*

C. Stanley, A. Ganguly, C. Macmullen, 2006, Journal of Biological Chemistry.

Histopathology of Congenital Hyperinsulinism: Retrospective Study with Genotype Correlations

C. Stanley, A. Ganguly, C. Macmullen, 2003, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Clinical and molecular characterization of a dominant form of congenital hyperinsulinism caused by a mutation in the high-affinity sulfonylurea receptor.

C. Stanley, L. Aguilar-Bryan, A. Ganguly, 2003, Diabetes.

Genetic association of cyclic AMP signaling genes with bipolar disorder

Dajiang J. Liu, S. Leal, R. Davis, 2012, Translational Psychiatry.

Genotype-phenotype correlations in children with congenital hyperinsulinism due to recessive mutations of the adenosine triphosphate-sensitive potassium channel genes.

C. Stanley, A. Ganguly, C. Macmullen, 2005, The Journal of clinical endocrinology and metabolism.

Familial leucine-sensitive hypoglycemia of infancy due to a dominant mutation of the beta-cell sulfonylurea receptor.

C. Stanley, A. Ganguly, C. Macmullen, 2004, The Journal of clinical endocrinology and metabolism.

Accuracy of [18F]fluorodopa positron emission tomography for diagnosing and localizing focal congenital hyperinsulinism.

Janet R. Saffer, A. Alavi, C. Stanley, 2007, The Journal of clinical endocrinology and metabolism.

Clinical characteristics and biochemical mechanisms of congenital hyperinsulinism associated with

C. Stanley, C. Macmullen, S. Shyng, 2008 .

Preoperative evaluation of infants with focal or diffuse congenital hyperinsulinism by intravenous acute insulin response tests and selective pancreatic arterial calcium stimulation.

C. Stanley, A. Ganguly, C. Macmullen, 2004, The Journal of clinical endocrinology and metabolism.

Hyperinsulinism/hyperammonemia syndrome in children with regulatory mutations in the inhibitory guanosine triphosphate-binding domain of glutamate dehydrogenase.

C. Stanley, T. Smith, A. Ganguly, 2001, The Journal of clinical endocrinology and metabolism.

Molecular and immunohistochemical analyses of the focal form of congenital hyperinsulinism

C. Stanley, A. Ganguly, C. Macmullen, 2006, Modern Pathology.

Congenital Hyperinsulinism: Intraoperative Biopsy Interpretation Can Direct the Extent of Pancreatectomy

C. Stanley, A. Ganguly, C. Macmullen, 2004, The American journal of surgical pathology.

Neuron-based high-content assay and screen for CNS active mitotherapeutics

Ronald L. Davis, Sathyanarayanan V. Puthanveettil, R. Pacifico, 2020, Science Advances.

Congenital Hyperinsulinism–Associated ABCC8 Mutations That Cause Defective Trafficking of ATP-Sensitive K+ Channels

C. Stanley, A. Ganguly, C. Macmullen, 2007, Diabetes.

Effects of a GTP-insensitive Mutation of Glutamate Dehydrogenase on Insulin Secretion in Transgenic Mice*♦

Thomas J Petty, C. Stanley, I. Nissim, 2006, Journal of Biological Chemistry.

Histologic and Molecular Profile of Pediatric Insulinomas: Evidence of a Paternal Parent-of-Origin Effect.

C. Stanley, A. Ganguly, L. Conlin, 2016, The Journal of clinical endocrinology and metabolism.

Genotype and phenotype correlations in 417 children with congenital hyperinsulinism.

C. Stanley, A. Ganguly, C. Macmullen, 2013, The Journal of clinical endocrinology and metabolism.

A Mutation in the TMD0-L0 Region of Sulfonylurea Receptor-1 (L225P) Causes Permanent Neonatal Diabetes Mellitus (PNDM)

C. Stanley, C. Nichols, C. Macmullen, 2007, Diabetes.

Novel, primate-specific PDE10A isoform highlights gene expression complexity in human striatum with implications on the molecular pathology of bipolar disorder

M. Fallahi-Sichani, R. Davis, R. Pacifico, 2016, Translational Psychiatry.

Dopamine Receptor DAMB Signals via Gq to Mediate Forgetting in Drosophila.

Ronald L. Davis, Jacob A. Berry, Ronald L Davis, 2017, Cell reports.

Novel PDE10A transcript diversity in the human striatum: Insights into gene complexity, conservation and regulation.

Ronald L. Davis, Mohammad Fallahi, Ronald L Davis, 2017, Gene.

Clinical characteristics and biochemical mechanisms of congenital hyperinsulinism associated with dominant KATP channel mutations.

Arupa Ganguly, C. Stanley, A. Ganguly, 2008, The Journal of clinical investigation.

Brain transcriptome changes in the aging Drosophila melanogaster accompany olfactory memory performance deficits

Ronald L. Davis, R. Pacifico, C. Macmullen, 2018, PloS one.

Destabilization of ATP-sensitive Potassium Channel Activity by Novel KCNJ11 Mutations Identified in Congenital Hyperinsulinism*

C. Stanley, A. Ganguly, C. Macmullen, 2008, Journal of Biological Chemistry.

Scribble Scaffolds a Signalosome for Active Forgetting

Ronald L. Davis, C. Macmullen, Isaac Cervantes-Sandoval, 2016, Neuron.

Dominant Form of Congenital Hyperinsulinism Maps to HK1 Region on 10q

H. Hakonarson, J. Bradfield, C. Stanley, 2013, Hormone Research in Paediatrics.

Diazoxide-Unresponsive Congenital Hyperinsulinism in Children With Dominant Mutations of the β-Cell Sulfonylurea Receptor SUR1

C. Stanley, A. Ganguly, C. Macmullen, 2011, Diabetes.

Interrogating the Spatiotemporal Landscape of Neuromodulatory GPCR Signaling by Real-Time Imaging of cAMP in Intact Neurons and Circuits

Ronald L. Davis, R. Blakely, S. Zucca, 2018, Cell reports.

Interrogating the Spatiotemporal Landscape of Neuromodulatory GPCR Signaling by Real-Time Imaging of cAMP in Intact Neurons and Circuits.

Ronald L. Davis, R. Blakely, S. Zucca, 2018, Cell reports.

Diazoxide-unresponsive congenital hyperinsulinism in children with dominant mutations of the β-cell sulfonylurea receptor SUR1 (Diabetes (2011) 60, (1797-1804))

C. Stanley, A. Ganguly, C. Macmullen, 2011 .

High-Throughput Phenotypic Assay for Compounds That Influence Mitochondrial Health Using iPSC-Derived Human Neurons

Ronald L. Davis, C. Macmullen, 2021, SLAS discovery : advancing life sciences R & D.