Magel2

The Nterminal domain of the SchaafYang syndrome protein MAGEL2 likely

MAGEL2 pathophysiology and SchaafYang syndrome Schubert 2025

Inside the Cell MAGEL2 Mislocalization and What It Means for SYS Research

Truncated variants of MAGEL2 are involved in the etiologies of the

The Nterminal domain of the SchaafYang syndrome protein MAGEL2 likely

MAGEL2 pathophysiology and SchaafYang syndrome EACD Galway 2026

a MAGEL2 variants and protein domain structures Truncating MAGEL2

Truncated variants of MAGEL2 are involved in the etiologies of the

Schematic structure of the human MAGEL2 and mice Magel2 A Human

Magel2 knockdown in hypothalamic POMC neurons innervating the medial

a MAGEL2 variants and protein domain structures Truncating MAGEL2

Loss of MAGEL2 in PraderWilli syndrome leads to decreased secretory

The Nterminal domain of the SchaafYang syndrome protein MAGEL2 likely

Magel2 promotes neurite outgrowth A Relative expression of Magel2

MAGEL2 is expressed in specific brain regions A Western blot

The Nterminal domain of the SchaafYang syndrome protein MAGEL2 likely

Targeted disruption of the Magel2 gene A Maps of the Magel2

Truncated variants of MAGEL2 are involved in the etiologies of the

Magel2 mRNA expression in the postnatal hypothalamus Relative

MAGEL2 modulates the subcellular localization of CRY1 and MAGEL2

Truncated variants of MAGEL2 are involved in the etiologies of the

Expression and distribution of Magel2 in the mouse brain A

MAGEL2 is involved in PraderWilli syndrome PWS and Schaafyang

Truncated variants of MAGEL2 are involved in the etiologies of the

Comparison of Magel2 and Ndn expression patterns in the E105 and E125

Expression patterns of the Magel2 transcript visualized using LacZ

Magel2 null mice have fewer ARC POMC neurons AB Representative

The Nterminal domain of the SchaafYang syndrome protein MAGEL2 likely

Magel2 interacts with Bmal1 and Per2 A HEK293 cells were transfected

Localization of the MAGEL2 gene in the 15q11q13 imprinting domain The

Magel2 deficient pups emit ultrasonic vocalizations with discrete

Maternal retrieval behavior is biased towards wildtype versus Magel2

Generation of NDN KO and MAGEL2 KO iPS cells A Genome sequencing was

Expression analysis of MAGEL2 a RTPCR analysis demonstrating MAGEL2

Generation of NDN KO and MAGEL2 KO iPS cells A Genome sequencing was

Simplified model for the role of MAGEL2 in circadian rhythm CLOCK and

Frontiers Magel2 in hypothalamic POMC neurons influences the impact

Expression and distribution of Magel2 in the mouse brain A

MAGEL2 mutations by location Graphical depiction of all 115 known

Figure 1 from The human MAGEL2 gene and its mouse homologue are

MAGEL2 is involved in PraderWilli syndrome PWS and Schaafyang

Genomic organization of the human and mouse MAGEL2 genes A The

Magel2 deficient pups emit ultrasonic vocalizations of distinct

PDF Clinical phenotypes of MAGEL2 mutations and deletions

Magel2 interacts with Bmal1 and Per2 A HEK293 cells were transfected

Magel2 deficiency increases cfos expression in SST neurons of dorsal

Human MAGEL2 expression during embryonic development A CS16 the

Truncated variants of MAGEL2 are involved in the etiologies of the

MAGEL2 is involved in PraderWilli syndrome PWS and Schaafyang

Magel2 deficient pups emit ultrasonic vocalizations of distinct

Unique MAGEL2 Findings Point to Potential PWS and SYS Genetic Therapy

JCI Insight Loss of MAGEL2 in PraderWilli syndrome leads to

Coexpression of MAGEL2 reduces the abundance of CRY1 A U2OS cells

Generation of NDN KO and MAGEL2 KO iPS cells A Genome sequencing was

Deficiency of the paternally inherited gene Magel2 alters the

Detection of MAGEL2 peptides in Magel2 mutant rats and SYS hiPSC lines

Subcellular localisation of truncated MAGEL2 proteins insight into the

Magel2 deficiency increases cfos expression in SST neurons of dorsal

Figure 1 from Loss of MAGEL2 in PraderWilli syndrome leads to

Magel2 deficiency decreases AVP receptors levels in SST neurons of

Table 1 from The human MAGEL2 gene and its mouse homologue are

Magel2 mRNA expression in the postnatal hypothalamus Relative

Figure 3 from The human MAGEL2 gene and its mouse homologue are

MAGEL2 is expressed in specific brain regions A Western blot

Coexpression of MAGEL2 reduces the abundance of CRY1 A U2OS cells

Magel2 represses ClockBmal1mediated transcription at an Ebox

MAGEL2 modulates the subcellular localization of CRY1 and MAGEL2

Genomic organization of the human and mouse MAGEL2 genes A The

Magel2 knockdown in hypothalamic POMC neurons innervating the medial

MAGEL2 is in proximity to RBX1 as detected by BioID U2OS cells were

Magel2 deficiency impairs the number of fibers projecting in dorsal LS

The excitatorytoinhibitory developmental GABA shift in Magel2 KO

Loss of MAGEL2 in PraderWilli syndrome leads to decreased secretory

Loss of the Magel2 gene in ARC POMC neurons innervating the MeA does

Expression analysis of MAGEL2 a RTPCR analysis demonstrating MAGEL2

MAGEL2 is in proximity to RBX1 as detected by BioID U2OS cells were

Loss of MAGEL2 in PraderWilli syndrome leads to decreased secretory

Magel2 is required for the leptininduced depolarizing response in POMC

De Novo Truncating Mutation Occurring on the Paternal MAGEL2 Allele in

Subcellular localisation of truncated MAGEL2 proteins insight into the

Magel2 deficiency affects the emission of ultrasonic vocalizations in

Frontiers Magel2 in hypothalamic POMC neurons influences the impact

Expression analysis of MAGEL2 a RTPCR analysis demonstrating MAGEL2

PDF Subcellular localization of truncated MAGEL2 proteins insight

Subcellular localisation of truncated MAGEL2 proteins insight into the

Magel2 knockdown in hypothalamic POMC neurons innervating the medial

Unique MAGEL2 Findings Point to Potential PWS and SYS Genetic Therapy

Frontiers Magel2 in hypothalamic POMC neurons influences the impact

Deficiency of the paternally inherited gene Magel2 alters the

Schematic structure of the human MAGEL2 and mice Magel2 A Human

Expression analysis of MAGEL2 a RTPCR analysis demonstrating MAGEL2

Hypothalamic AAVBDNF gene therapy improves metabolic function and

Advancing in SchaafYang syndrome pathophysiology from bedside to

Frontiers Cellspecific secretory granule sorting mechanisms the

Biochemical pathway showing the role of MAGEL2 mediated WASH complex

Advancing in SchaafYang syndrome pathophysiology from bedside to

Human Genetics and Genomics Advances Human Genetics and Genomics Advances

Truncating mutations of MAGEL2cause PraderWilli phenotypes and autism

Truncating mutations on the paternal allele of MAGEL2 a GC content

Paternal origin of MAGEL2Magel2 gene expression A RTPCR analysis

Truncating Mutations of MAGEL2 a Gene within the PraderWilli Locus

Mapping genomic structure and transcript of Magel2 a Mapping of

Similarity of the 240 MAGEL2Magel2 Cterminal amino acids with

A MAGEL2deubiquitinase complex modulates the ubiquitination of

Hypothalamic AAVBDNF gene therapy improves metabolic function and

JCI Insight Investigation of a mouse model of PraderWilli syndrome

Figure 1 from Truncating Mutations of MAGEL2 a Gene within the Prader

ARC POMC neurons express MAGEL2 A Images of confocal fluorescence

JCI Insight Investigation of a mouse model of PraderWilli Syndrome

Comprehensive insilico molecular analysis of earlyonset gastric

Frontiers Cellspecific secretory granule sorting mechanisms the

Hypothalamic AAVBDNF gene therapy improves metabolic function and

JCI Insight Investigation of a mouse model of PraderWilli Syndrome

Central ER-α does not contribute to the regulation of locomotor ...

Central ER does not contribute to the regulation of locomotor

Investigation of a mouse model of PraderWilli Syndrome with combined

Human Genetics and Genomics Advances Human Genetics and Genomics Advances

Sequence comparisons among MAGEL2 NDN and their murine orthologs A

Frontiers Cellspecific secretory granule sorting mechanisms the

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