Investigator and Section Head, Translational Physiology, Diabetes, Endocrinology, and Obesity Branch, NIDDK, NIH
Endocrinology
Dr. Aaron M. Cypess, MD
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Aaron Cypess is an expert in the field of Endocrinology. He went to Weill Cornell Medical College of Cornell University. Weill Cornell Medical College of Cornell University has a rank of 18 in research and a 49 in primary care He received awards:"CMS Meaningful Use Stage 1 Certification", "Diabetes Recognition Program" and "Whos Who in Medicine and Healthcare". Dr. Aaron M. Cypess is a published doctor as well. He has 34 publications published. The latest was: Antibodies against specific extracellular epitopes of the glucagon receptor block glucagon binding. Aaron M. Cypess, MD accepts Medicare payments and is registered with Medicare.gov.
Publications
- Contrast-Enhanced Ultrasound: A Novel Noninvasive, Nonionizing Method for the Detection of Brown Adipose Tissue in Humans.
- Genetic and functional characterization of clonally derived adult human brown adipocytes.
- Activation of human brown adipose tissue by a β3-adrenergic receptor agonist.
- IRF4 Is a Key Thermogenic Transcriptional Partner of PGC-1α.
- Quantification of Human and Rodent Brown Adipose Tissue Function Using 99mTc-Methoxyisobutylisonitrile SPECT/CT and 18F-FDG PET/CT.
- Measurement of Human Brown Adipose Tissue Volume and Activity Using Anatomic MR Imaging and Functional MR Imaging.
- Anatomical localization, gene expression profiling and functional characterization of adult human neck brown fat.
- Brown-fat paucity due to impaired BMP signalling induces compensatory browning of white fat.
- Increased FDG uptake in association With reduced extremity fat in HIV patients.
- Anatomical and functional assessment of brown adipose tissue by magnetic resonance imaging.
- Deiodinase 2 Expression Is Increased in Dorsocervical Fat of Patients With HIV-Associated Lipohypertrophy Syndrome.
- Insulin/IGF-I Regulation of Necdin and Brown Adipocyte Differentiation Via CREB- and FoxO1-Associated Pathways.
- Pediatric Brown Adipose Tissue: Detection, Epidemiology, and Differences from Adults.
- A New Connection between Muscle and Brown Fat.
- The role and importance of brown adipose tissue in energy homeostasis.
- Insulin enhances glucose-stimulated insulin secretion in healthy humans.
- Identification and importance of brown adipose tissue in adult humans.
- Uncommon presentations of some common malignancies: Case 1. Sequential paraneoplastic endocrine Syndromes in small-cell lung cancer.
- Cellular bioenergetics as a target for Obesity therapy.
- Exogenous insulin enhances glucose-stimulated insulin response in healthy humans independent of changes in free fatty acids.
- Brown fat as a therapy for obesity and Diabetes.
- Prediction of preadipocyte differentiation by gene expression reveals role of insulin receptor substrates and necdin.
- Determination of cytosine-beta-D-arabinoside in plasma using capillary electrophoresis.
- Measurement of skin-to-kidney distance in children: implications for quantitative renography.
- Characterization of deletion and truncation mutants of the rat glucagon receptor. Seven transmembrane segments are necessary for receptor transport to the plasma membr...
- Calcium regulates processing of the Alzheimer amyloid protein precursor in a protein kinase C-independent manner.
- Characterization of mutant rhodopsins responsible for autosomal dominant retinitis pigmentosa. Mutations on the cytoplasmic surface affect transducin activation.
- Antibodies against specific extracellular epitopes of the glucagon receptor block glucagon binding.
- Two cytoplasmic loops of the glucagon receptor are required to elevate cAMP or intracellular Calcium.
- Calcitonin gene-related peptide decreases expression of HLA-DR and CD86 by human dendritic cells and dampens dendritic cell-driven T cell-proliferative responses via t...
- Selective reconstitution of human D4 dopamine receptor variants with Gi alpha subTypes.
- Glucagon receptor activates extracellular signal-regulated protein kinase 1/2 via cAMP-dependent protein kinase.
- Modulation of glucagon receptor expression and response in transfected human embryonic kidney cells.
Schools
Joan Sanford I Weill Medical College Of Cornell University
Beth Israel Deaconess Med Center
Procedures Preformed
- Continuous Glucose Monitoring
Conditions Treated
- Adrenal Insufficiency
- Calcium Metabolism Disorders
- Diabetes Type 1
- Diabetes Type 2
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Doctors Specialties
- Endocrinology
Accepted Insurances
Awards
- CMS Meaningful Use Stage 1 Certification
- Diabetes Recognition Program
- Whos Who in Medicine and Healthcare
Education
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Beth Israel Deaconess Medical Center -
Weill Cornell Medical College of Cornell University
Hospital
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Beth Israel Deaconess Medical Center
Drug Facts
| NPI NUMBER | 1598730749 | |
| NPPES Provider LastName | CYPESS | |
| NPPES Provider FirstName | AARON | |
| NPPES Provider ZIPCode | 022155400 | |
| NPPES Provider State | MA | |
| Specialty Description | Endocrinology | |
| Total Claim Count | 502.0 | |
| Distinct Opioid Count | 0.0 | |
| Opioid Claim Count | 0.0 | |
| Percent Opioid Claims | 0.0 |
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1598730749 |
| Last Name Of The Provider | CYPESS |
| First Name Of The Provider | AARON |
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