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IPW gene

Known as: imprinted in Prader-Willi syndrome (non-protein coding), IMPRINTED IN PRADER-WILLI SYNDROME, IPW 
National Institutes of Health

Papers overview

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2015
2015
Background Quasi-experimental studies of menu labeling have found mixed results for improving diet. Differences between… 
2014
2014
This paper considers treatment evaluation in a discrete time setting in which treatment could start at any point in time. A… 
2014
2014
Prader-Willi syndrome (PWS) is caused by loss of paternally expressed genes at an imprinted locus on chromosome 15, including the… 
2014
2014
Device interactions between ESD diodes and NMOS clamps are analyzed in three different example layout configurations using… 
2013
2013
This paper estimates the labor market effects of being awarded with a training voucher using an instrumental variable approach… 
2010
2010
We theoretically describe the spin excitation spectrum of a two dimensional electron gas embedded in a quantum well with… 
Highly Cited
2000
Highly Cited
2000
Prader-Willi syndrome (PWS) is a neurogenetic disease characterized by infantile hypotonia, gonadal hypoplasia, obsessive… 
2000
2000
An Instrument Surveillance and Calibration Verification (ISCV) system primarily consists of a process model, which is used to… 
1996
1996
IPW (Imprinted gene in the Prader-Willi syndrome region) is a recently identified paternally expressed gene. Previous work has…