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List of works by Rachel Wevrick

A MAGE/NDN-like gene in zebrafish

scientific article

A MAGEL2-deubiquitinase complex modulates the ubiquitination of circadian rhythm protein CRY1

scientific article published on 21 April 2020

A mouse model for Prader-Willi syndrome imprinting-centre mutations

scientific article

An imprinted mouse transcript homologous to the human imprinted in Prader-Willi syndrome (IPW) gene.

scientific article

Chromatin modification of the human imprinted NDN (necdin) gene detected by in vivo footprinting

scientific article published on 01 April 2005

Chronic diazoxide treatment decreases fat mass and improves endurance capacity in an obese mouse model of Prader-Willi syndrome

scientific article published in April 2018

Claudin-4 forms a paracellular barrier, revealing the interdependence of claudin expression in the loose epithelial cell culture model opossum kidney cells.

scientific article

Cloning and analysis of the murine Fanconi anemia group C cDNA.

scientific article published in June 1993

Co-morbidity of complex genetic disorders and hypersomnias of central origin: lessons from the underlying neurobiology of wake and sleep.

scientific article published on 25 April 2012

Diagnostic test for the Prader-Willi syndrome by SNRPN expression in blood

scientific article published in October 1996

Disruption of the mouse necdin gene results in early post-natal lethality

scientific journal article

Dopamine pathway imbalance in mice lacking Magel2, a Prader-Willi syndrome candidate gene

scientific article

Energy homeostasis in Prader-Willi Syndrome: How clinical research informs studies of animal models of genetic obesity

scientific article published on 14 March 2012

Essential role for the Prader-Willi syndrome protein necdin in axonal outgrowth

scientific journal article

Establishment and maintenance of DNA methylation patterns in mouse Ndn: implications for maintenance of imprinting in target genes of the imprinting center.

scientific article published on April 2001

Evaluation of melanoma antigen (MAGE) gene expression in human cancers using The Cancer Genome Atlas.

scientific article published on 29 November 2014

Expression of the Fanconi anemia gene FAC in human cell lines: lack of effect of oxygen tension.

scientific article published on January 1995

Genetic analysis of very obese children with autism spectrum disorder

scientific article published on 11 January 2018

Genome-wide analysis of gene transcription in the hypothalamus

scientific article published on 3 May 2005

Human centromeric DNAs.

scientific article published on September 1997

Impaired hypothalamic regulation of endocrine function and delayed counterregulatory response to hypoglycemia in Magel2-null mice.

scientific article

Inactivation of the mouse Magel2 gene results in growth abnormalities similar to Prader-Willi syndrome

article

Leptin signaling defects in a mouse model of Prader-Willi syndrome: An orphan genetic obesity syndrome no more?

scientific article published on 27 March 2013

Long-range organization of tandem arrays of alpha satellite DNA at the centromeres of human chromosomes: high-frequency array-length polymorphism and meiotic stability.

scientific article

Loss of Necdin impairs myosin activation and delays cell polarization ⬇️

scientific article published on September 1, 2010

Loss of magel2, a candidate gene for features of Prader-Willi syndrome, impairs reproductive function in mice

scientific article

Loss of the Prader-Willi obesity syndrome protein necdin promotes adipogenesis.

scientific article published on 27 January 2012

Loss of the Prader-Willi syndrome protein necdin causes defective migration, axonal outgrowth, and survival of embryonic sympathetic neurons

scientific article published in July 2008

Magel2 Is Required for Leptin-Mediated Depolarization of POMC Neurons in the Hypothalamic Arcuate Nucleus in Mice ⬇️

scientific article published on January 17, 2013

Magel2, a Prader-Willi syndrome candidate gene, modulates the activities of circadian rhythm proteins in cultured cells

scientific journal article

Magel2-null mice are hyper-responsive to setmelanotide, a melanocortin 4 receptor agonist

scientific article published on 24 June 2016

Mapping of the murine and rat Facc genes and assessment of flexed-tail as a candidate mouse homolog of Fanconi anemia group C

scientific article published on 01 January 1993

Muscle dysfunction caused by loss of Magel2 in a mouse model of Prader-Willi and Schaaf-Yang syndromes.

scientific article published on 19 July 2016

Necdin, a Prader-Willi syndrome candidate gene, regulates gonadotropin-releasing hormone neurons during development.

scientific article published on 17 October 2008

Necdin, a p53 target gene, regulates the quiescence and response to genotoxic stress of hematopoietic stem/progenitor cells.

scientific article

Partial deletion of alpha satellite DNA associated with reduced amounts of the centromere protein CENP-B in a mitotically stable human chromosome rearrangement

scientific article published on December 1990

Physical map of the centromeric region of human chromosome 7: relationship between two distinct alpha satellite arrays

scientific article published on May 1991

Prader-Willi syndrome transcripts are expressed in phenotypically significant regions of the developing mouse brain

scientific article

Progressive postnatal decline in leptin sensitivity of arcuate hypothalamic neurons in the Magel2-null mouse model of Prader-Willi syndrome

scientific article published on 29 April 2015

Pulsed-field and two-dimensional gel electrophoresis of long arrays of tandemly repeated DNA : analysis of human centromeric alpha satellite

scientific article published on 01 January 1992

Regionally reduced brain volume, altered serotonin neurochemistry, and abnormal behavior in mice null for the circadian rhythm output gene Magel2.

scientific article published in December 2009

Regulation of autism-relevant behaviors by cerebellar-prefrontal cortical circuits

scientific article published on 13 July 2020

Sleeve gastrectomy leads to weight loss in the Magel2 knockout mouse

scientific article

Stochastic loss of silencing of the imprinted Ndn/NDN allele, in a mouse model and humans with prader-willi syndrome, has functional consequences

scientific article

Structure of DNA near long tandem arrays of alpha satellite DNA at the centromere of human chromosome 7.

scientific article published in December 1992

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

scientific article published on 22 October 2016

The Prader-Willi syndrome protein necdin interacts with the E1A-like inhibitor of differentiation EID-1 and promotes myoblast differentiation

scientific article

The Prader-Willi syndrome proteins MAGEL2 and necdin regulate leptin receptor cell surface abundance through ubiquitination pathways

scientific article published on 14 August 2017

The Smc5/Smc6/MAGE complex confers resistance to caffeine and genotoxic stress in Drosophila melanogaster

scientific article

The imprinted gene Magel2 regulates normal circadian output

scientific article published on 23 September 2007

The necdin gene is deleted in Prader-Willi syndrome and is imprinted in human and mouse

scientific article

The necdin interactome: evaluating the effects of amino acid substitutions and cell stress using proximity-dependent biotinylation (BioID) and mass spectrometry

scientific article published on 11 June 2020

Tissue-specific and imprinted epigenetic modifications of the human NDN gene

scientific article

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