4.7 Article

Effects of thermoneutrality on food intake, body weight, and body composition in a Prader-Willi syndrome mouse model

Related references

Note: Only part of the references are listed.
Article Cell Biology

Mouse Thermoregulation: Introducing the Concept of the Thermoneutral Point

Vojtech Skop et al.

CELL REPORTS (2020)

Article Endocrinology & Metabolism

Prader-Willi syndrome: A model for understanding the ghrelin system

Maithe Tauber et al.

JOURNAL OF NEUROENDOCRINOLOGY (2019)

Article Endocrinology & Metabolism

Thermoneutrality improves skeletal impairment in adult Prader-Willi syndrome mice

Thomas M. Braxton et al.

JOURNAL OF ENDOCRINOLOGY (2019)

Editorial Material Medicine, Research & Experimental

Hypothalamic loss of Snord116 and Prader-Willi syndrome hyperphagia: the buck stops here?

Juan A. Rodriguez et al.

JOURNAL OF CLINICAL INVESTIGATION (2018)

Article Medicine, Research & Experimental

Hypothalamic loss of Snord116 recapitulates the hyperphagia of Prader-Willi syndrome

Joseph Polex-Wolf et al.

JOURNAL OF CLINICAL INVESTIGATION (2018)

Article Endocrinology & Metabolism

Ghrelin Receptor Agonist Rescues Excess Neonatal Mortality in a Prader-Willi Syndrome Mouse Model

Juan A. Rodriguez et al.

ENDOCRINOLOGY (2018)

Article Medicine, Research & Experimental

Deficiency in prohormone convertase PC1 impairs prohormone processing in Prader-Willi syndrome

Lisa C. Burnett et al.

JOURNAL OF CLINICAL INVESTIGATION (2017)

Article Endocrinology & Metabolism

Paradoxical leanness in the imprinting-centre deletion mouse model for Prader-Willi syndrome

David M. Golding et al.

JOURNAL OF ENDOCRINOLOGY (2017)

Article Endocrinology & Metabolism

Targeting the endocannabinoid/CB1 receptor system for treating obesity in Pradere-Willi syndrome

Ibrahim Knani et al.

MOLECULAR METABOLISM (2016)

Article Multidisciplinary Sciences

Snord116 is critical in the regulation of food intake and body weight

Yue Qi et al.

SCIENTIFIC REPORTS (2016)

Article Biochemistry & Molecular Biology

Highly restricted deletion of the SNORD116 region is implicated in Prader-Willi Syndrome

Eric Bieth et al.

EUROPEAN JOURNAL OF HUMAN GENETICS (2015)

Article Genetics & Heredity

Hypoglycemia in Prader-Willi Syndrome

Rena A. Harrington et al.

AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2014)

Review Endocrinology & Metabolism

Mouse models of Prader-Willi Syndrome: A systematic review

Sandrina Bervini et al.

FRONTIERS IN NEUROENDOCRINOLOGY (2013)

Review Biochemistry & Molecular Biology

Recommendations for the investigation of animal models of Prader-Willi syndrome

James L. Resnick et al.

MAMMALIAN GENOME (2013)

Article Biochemistry & Molecular Biology

Unique and atypical deletions in Prader-Willi syndrome reveal distinct phenotypes

Soo-Jeong Kim et al.

EUROPEAN JOURNAL OF HUMAN GENETICS (2012)

Review Genetics & Heredity

Prader-Willi syndrome

Suzanne B. Cassidy et al.

GENETICS IN MEDICINE (2012)

Article Endocrinology & Metabolism

Approach to the Child with Prader-Willi Syndrome

Jennifer L. Miller

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2012)

Review Immunology

Unstressing intemperate models: how cold stress undermines mouse modeling

Christopher L. Karp

JOURNAL OF EXPERIMENTAL MEDICINE (2012)

Article Education, Special

Psychiatric illness in a cohort of adults with Prader-Willi syndrome

Margje Sinnema et al.

RESEARCH IN DEVELOPMENTAL DISABILITIES (2011)

Article Biochemistry & Molecular Biology

Paternally inherited microdeletion at 15q11.2 confirms a significant role for the SNORD116 C/D box snoRNA cluster in Prader-Willi syndrome

Angela L. Duker et al.

EUROPEAN JOURNAL OF HUMAN GENETICS (2010)

Article Endocrinology & Metabolism

Phenotyping small animals as models for the human metabolic syndrome: thermoneutrality matters

J. M. Overton

INTERNATIONAL JOURNAL OF OBESITY (2010)

Article Orthopedics

The Musculoskeletal Manifestations of Prader-Willi Syndrome

Jong Sup Shim et al.

JOURNAL OF PEDIATRIC ORTHOPAEDICS (2010)

Article Biochemistry & Molecular Biology

A deletion of the HBII-85 class of small nucleolar RNAs (snoRNAs) is associated with hyperphagia, obesity and hypogonadism

Adam J. de Smith et al.

HUMAN MOLECULAR GENETICS (2009)

Article Endocrinology & Metabolism

Randomized Controlled Trial to Investigate the Effects of Growth Hormone Treatment on Scoliosis in Children with Prader-Willi Syndrome

Roderick F. A. de Lind van Wijngaarden et al.

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2009)

Article Biochemistry & Molecular Biology

Lack of Pwcr1/MBII-85 snoRNA is critical for neonatal lethality in Prader-Willi syndrome mouse models

F Ding et al.

MAMMALIAN GENOME (2005)

Article Biochemistry & Molecular Biology

Evidence for genetic modifiers of postnatal lethality in PWS-IC deletion mice

SJ Chamberlain et al.

HUMAN MOLECULAR GENETICS (2004)

Review Endocrinology & Metabolism

Prader-Willi syndrome: advances in genetics, pathophysiology and treatment

AP Goldstone

TRENDS IN ENDOCRINOLOGY AND METABOLISM (2004)

Article Endocrinology & Metabolism

Validation of whole-body magnetic resonance spectroscopy as a tool to assess murine body composition

P Mystkowski et al.

INTERNATIONAL JOURNAL OF OBESITY (2000)