Oxytocin's Regulation of Thermogenesis May Be the Link to Prader-Willi Syndrome
Curr Issues Mol Biol. 2023 Jun 6;45(6):4923-4935. doi: 10.3390/cimb45060313.ABSTRACTPrader-Willi Syndrome (PWS) is a genetic neurodevelopmental disorder that is caused by either the deletion of the paternal allele of 15q11-q13, maternal uniparental disomy of chromosome 15 or defects in the chromosome 15 imprinting centre and is characterized by cognitive impairment, hyperphagia and low metabolic rate with significant risk of obesity, as well as a variety of other maladaptive behaviours and autistic spectrum disorder (ASD). Many of the features seen in PWS are thought to be due to hypothalamic dysfunction resulting in hormo...
Source: Current Issues in Molecular Biology - June 27, 2023 Category: Molecular Biology Authors: Claudia Camerino Source Type: research
Oxytocin's Regulation of Thermogenesis May Be the Link to Prader-Willi Syndrome
Curr Issues Mol Biol. 2023 Jun 6;45(6):4923-4935. doi: 10.3390/cimb45060313.ABSTRACTPrader-Willi Syndrome (PWS) is a genetic neurodevelopmental disorder that is caused by either the deletion of the paternal allele of 15q11-q13, maternal uniparental disomy of chromosome 15 or defects in the chromosome 15 imprinting centre and is characterized by cognitive impairment, hyperphagia and low metabolic rate with significant risk of obesity, as well as a variety of other maladaptive behaviours and autistic spectrum disorder (ASD). Many of the features seen in PWS are thought to be due to hypothalamic dysfunction resulting in hormo...
Source: Current Issues in Molecular Biology - June 27, 2023 Category: Molecular Biology Authors: Claudia Camerino Source Type: research
Oxytocin's Regulation of Thermogenesis May Be the Link to Prader-Willi Syndrome
Curr Issues Mol Biol. 2023 Jun 6;45(6):4923-4935. doi: 10.3390/cimb45060313.ABSTRACTPrader-Willi Syndrome (PWS) is a genetic neurodevelopmental disorder that is caused by either the deletion of the paternal allele of 15q11-q13, maternal uniparental disomy of chromosome 15 or defects in the chromosome 15 imprinting centre and is characterized by cognitive impairment, hyperphagia and low metabolic rate with significant risk of obesity, as well as a variety of other maladaptive behaviours and autistic spectrum disorder (ASD). Many of the features seen in PWS are thought to be due to hypothalamic dysfunction resulting in hormo...
Source: Current Issues in Molecular Biology - June 27, 2023 Category: Molecular Biology Authors: Claudia Camerino Source Type: research
Oxytocin's Regulation of Thermogenesis May Be the Link to Prader-Willi Syndrome
Curr Issues Mol Biol. 2023 Jun 6;45(6):4923-4935. doi: 10.3390/cimb45060313.ABSTRACTPrader-Willi Syndrome (PWS) is a genetic neurodevelopmental disorder that is caused by either the deletion of the paternal allele of 15q11-q13, maternal uniparental disomy of chromosome 15 or defects in the chromosome 15 imprinting centre and is characterized by cognitive impairment, hyperphagia and low metabolic rate with significant risk of obesity, as well as a variety of other maladaptive behaviours and autistic spectrum disorder (ASD). Many of the features seen in PWS are thought to be due to hypothalamic dysfunction resulting in hormo...
Source: Current Issues in Molecular Biology - June 27, 2023 Category: Molecular Biology Authors: Claudia Camerino Source Type: research
Oxytocin's Regulation of Thermogenesis May Be the Link to Prader-Willi Syndrome
Curr Issues Mol Biol. 2023 Jun 6;45(6):4923-4935. doi: 10.3390/cimb45060313.ABSTRACTPrader-Willi Syndrome (PWS) is a genetic neurodevelopmental disorder that is caused by either the deletion of the paternal allele of 15q11-q13, maternal uniparental disomy of chromosome 15 or defects in the chromosome 15 imprinting centre and is characterized by cognitive impairment, hyperphagia and low metabolic rate with significant risk of obesity, as well as a variety of other maladaptive behaviours and autistic spectrum disorder (ASD). Many of the features seen in PWS are thought to be due to hypothalamic dysfunction resulting in hormo...
Source: Current Issues in Molecular Biology - June 27, 2023 Category: Molecular Biology Authors: Claudia Camerino Source Type: research
Oxytocin's Regulation of Thermogenesis May Be the Link to Prader-Willi Syndrome
Curr Issues Mol Biol. 2023 Jun 6;45(6):4923-4935. doi: 10.3390/cimb45060313.ABSTRACTPrader-Willi Syndrome (PWS) is a genetic neurodevelopmental disorder that is caused by either the deletion of the paternal allele of 15q11-q13, maternal uniparental disomy of chromosome 15 or defects in the chromosome 15 imprinting centre and is characterized by cognitive impairment, hyperphagia and low metabolic rate with significant risk of obesity, as well as a variety of other maladaptive behaviours and autistic spectrum disorder (ASD). Many of the features seen in PWS are thought to be due to hypothalamic dysfunction resulting in hormo...
Source: Current Issues in Molecular Biology - June 27, 2023 Category: Molecular Biology Authors: Claudia Camerino Source Type: research
Oxytocin's Regulation of Thermogenesis May Be the Link to Prader-Willi Syndrome
Curr Issues Mol Biol. 2023 Jun 6;45(6):4923-4935. doi: 10.3390/cimb45060313.ABSTRACTPrader-Willi Syndrome (PWS) is a genetic neurodevelopmental disorder that is caused by either the deletion of the paternal allele of 15q11-q13, maternal uniparental disomy of chromosome 15 or defects in the chromosome 15 imprinting centre and is characterized by cognitive impairment, hyperphagia and low metabolic rate with significant risk of obesity, as well as a variety of other maladaptive behaviours and autistic spectrum disorder (ASD). Many of the features seen in PWS are thought to be due to hypothalamic dysfunction resulting in hormo...
Source: Current Issues in Molecular Biology - June 27, 2023 Category: Molecular Biology Authors: Claudia Camerino Source Type: research
Oxytocin's Regulation of Thermogenesis May Be the Link to Prader-Willi Syndrome
Curr Issues Mol Biol. 2023 Jun 6;45(6):4923-4935. doi: 10.3390/cimb45060313.ABSTRACTPrader-Willi Syndrome (PWS) is a genetic neurodevelopmental disorder that is caused by either the deletion of the paternal allele of 15q11-q13, maternal uniparental disomy of chromosome 15 or defects in the chromosome 15 imprinting centre and is characterized by cognitive impairment, hyperphagia and low metabolic rate with significant risk of obesity, as well as a variety of other maladaptive behaviours and autistic spectrum disorder (ASD). Many of the features seen in PWS are thought to be due to hypothalamic dysfunction resulting in hormo...
Source: Current Issues in Molecular Biology - June 27, 2023 Category: Molecular Biology Authors: Claudia Camerino Source Type: research
Oxytocin's Regulation of Thermogenesis May Be the Link to Prader-Willi Syndrome
Curr Issues Mol Biol. 2023 Jun 6;45(6):4923-4935. doi: 10.3390/cimb45060313.ABSTRACTPrader-Willi Syndrome (PWS) is a genetic neurodevelopmental disorder that is caused by either the deletion of the paternal allele of 15q11-q13, maternal uniparental disomy of chromosome 15 or defects in the chromosome 15 imprinting centre and is characterized by cognitive impairment, hyperphagia and low metabolic rate with significant risk of obesity, as well as a variety of other maladaptive behaviours and autistic spectrum disorder (ASD). Many of the features seen in PWS are thought to be due to hypothalamic dysfunction resulting in hormo...
Source: Current Issues in Molecular Biology - June 27, 2023 Category: Molecular Biology Authors: Claudia Camerino Source Type: research
Oxytocin's Regulation of Thermogenesis May Be the Link to Prader-Willi Syndrome
Curr Issues Mol Biol. 2023 Jun 6;45(6):4923-4935. doi: 10.3390/cimb45060313.ABSTRACTPrader-Willi Syndrome (PWS) is a genetic neurodevelopmental disorder that is caused by either the deletion of the paternal allele of 15q11-q13, maternal uniparental disomy of chromosome 15 or defects in the chromosome 15 imprinting centre and is characterized by cognitive impairment, hyperphagia and low metabolic rate with significant risk of obesity, as well as a variety of other maladaptive behaviours and autistic spectrum disorder (ASD). Many of the features seen in PWS are thought to be due to hypothalamic dysfunction resulting in hormo...
Source: Current Issues in Molecular Biology - June 27, 2023 Category: Molecular Biology Authors: Claudia Camerino Source Type: research
Oxytocin's Regulation of Thermogenesis May Be the Link to Prader-Willi Syndrome
Curr Issues Mol Biol. 2023 Jun 6;45(6):4923-4935. doi: 10.3390/cimb45060313.ABSTRACTPrader-Willi Syndrome (PWS) is a genetic neurodevelopmental disorder that is caused by either the deletion of the paternal allele of 15q11-q13, maternal uniparental disomy of chromosome 15 or defects in the chromosome 15 imprinting centre and is characterized by cognitive impairment, hyperphagia and low metabolic rate with significant risk of obesity, as well as a variety of other maladaptive behaviours and autistic spectrum disorder (ASD). Many of the features seen in PWS are thought to be due to hypothalamic dysfunction resulting in hormo...
Source: Current Issues in Molecular Biology - June 27, 2023 Category: Molecular Biology Authors: Claudia Camerino Source Type: research
Oxytocin's Regulation of Thermogenesis May Be the Link to Prader-Willi Syndrome
Curr Issues Mol Biol. 2023 Jun 6;45(6):4923-4935. doi: 10.3390/cimb45060313.ABSTRACTPrader-Willi Syndrome (PWS) is a genetic neurodevelopmental disorder that is caused by either the deletion of the paternal allele of 15q11-q13, maternal uniparental disomy of chromosome 15 or defects in the chromosome 15 imprinting centre and is characterized by cognitive impairment, hyperphagia and low metabolic rate with significant risk of obesity, as well as a variety of other maladaptive behaviours and autistic spectrum disorder (ASD). Many of the features seen in PWS are thought to be due to hypothalamic dysfunction resulting in hormo...
Source: Current Issues in Molecular Biology - June 27, 2023 Category: Molecular Biology Authors: Claudia Camerino Source Type: research
Oxytocin's Regulation of Thermogenesis May Be the Link to Prader-Willi Syndrome
Curr Issues Mol Biol. 2023 Jun 6;45(6):4923-4935. doi: 10.3390/cimb45060313.ABSTRACTPrader-Willi Syndrome (PWS) is a genetic neurodevelopmental disorder that is caused by either the deletion of the paternal allele of 15q11-q13, maternal uniparental disomy of chromosome 15 or defects in the chromosome 15 imprinting centre and is characterized by cognitive impairment, hyperphagia and low metabolic rate with significant risk of obesity, as well as a variety of other maladaptive behaviours and autistic spectrum disorder (ASD). Many of the features seen in PWS are thought to be due to hypothalamic dysfunction resulting in hormo...
Source: Current Issues in Molecular Biology - June 27, 2023 Category: Molecular Biology Authors: Claudia Camerino Source Type: research
Oxytocin's Regulation of Thermogenesis May Be the Link to Prader-Willi Syndrome
Curr Issues Mol Biol. 2023 Jun 6;45(6):4923-4935. doi: 10.3390/cimb45060313.ABSTRACTPrader-Willi Syndrome (PWS) is a genetic neurodevelopmental disorder that is caused by either the deletion of the paternal allele of 15q11-q13, maternal uniparental disomy of chromosome 15 or defects in the chromosome 15 imprinting centre and is characterized by cognitive impairment, hyperphagia and low metabolic rate with significant risk of obesity, as well as a variety of other maladaptive behaviours and autistic spectrum disorder (ASD). Many of the features seen in PWS are thought to be due to hypothalamic dysfunction resulting in hormo...
Source: Current Issues in Molecular Biology - June 27, 2023 Category: Molecular Biology Authors: Claudia Camerino Source Type: research
Oxytocin's Regulation of Thermogenesis May Be the Link to Prader-Willi Syndrome
Curr Issues Mol Biol. 2023 Jun 6;45(6):4923-4935. doi: 10.3390/cimb45060313.ABSTRACTPrader-Willi Syndrome (PWS) is a genetic neurodevelopmental disorder that is caused by either the deletion of the paternal allele of 15q11-q13, maternal uniparental disomy of chromosome 15 or defects in the chromosome 15 imprinting centre and is characterized by cognitive impairment, hyperphagia and low metabolic rate with significant risk of obesity, as well as a variety of other maladaptive behaviours and autistic spectrum disorder (ASD). Many of the features seen in PWS are thought to be due to hypothalamic dysfunction resulting in hormo...
Source: Current Issues in Molecular Biology - June 27, 2023 Category: Molecular Biology Authors: Claudia Camerino Source Type: research
