Mice lacking <scp>proSAAS</scp> display alterations in emotion, consummatory behavior and circadian entrainment-Reference-Cited by-同舟云学术

Mice lacking proSAAS display alterations in emotion, consummatory behavior and circadian entrainment

Published:2022-07-25 Issue:7 Volume:21 Page:
ISSN:1601-1848
Container-title:Genes, Brain and Behavior
language:en
Short-container-title:Genes Brain and Behavior

Author:

Aryal Dipendra K.¹,Rodriguiz Ramona M.¹²,Nguyen Ngoc Lien¹,Pease Matthew W.¹^ORCID,Morgan Daniel J.³,Pintar John⁴,Fricker Lloyd D.⁵,Wetsel William C.²⁶⁷^ORCID

Affiliation:

1. Department of Psychiatry and Behavioral Sciences Duke University Medical Center Durham North Carolina USA

2. Department of Psychiatry and Behavioral Sciences, Mouse Behavioral and Neuroendocrine Analysis Core Facility Duke University Medical Center Durham North Carolina USA

3. Department of Anesthesiology and Perioperative Medicine, Pennsylvania State University College of Medicine Hershey Pennsylvania USA

4. Department of Neuroscience and Cell Biology Rutgers Robert Wood Johnson Medical School Piscataway New Jersey USA

5. Departments of Molecular Pharmacology and Neuroscience Albert Einstein College of Medicine Bronx New York USA

6. Department of Cell Biology Duke University Medical Center Durham North Carolina USA

7. Department of Neurobiology Duke University Medical Center Durham NC USA

Funder

National Institute on Drug Abuse

Pennsylvania Department of Health

Publisher

Wiley

Subject

Behavioral Neuroscience,Neurology,Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/gbb.12827

Reference56 articles.

1. Neuropeptides and Other Bioactive Peptides: From Discovery to Function

2. Carboxypeptidase E

3. Enkephalin convertase: purification and characterization of a specific enkephalin-synthesizing carboxypeptidase localized to adrenal chromaffin granules.

4. Identification and Characterization of proSAAS, a Granin-Like Neuroendocrine Peptide Precursor that Inhibits Prohormone Processing

5. The SAAS granin exhibits structural and functional homology to 7B2 and contains a highly potent hexapeptide inhibitor of PC1

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