(Q38330719)

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Genetic variants of the human obesity (OB) gene in subjects with and without Prader-Willi syndrome: comparison with body mass index and weight.

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scholarly article

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Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9842990%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

Genetic variants of the human obesity (OB) gene in subjects with and without Prader-Willi syndrome: comparison with body mass index and weight (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9842990%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

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Prader–Willi syndrome

1 reference

based on heuristic

inferred from title

Irene D. Feurer

4

object named as

I D Feurer

1 reference

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7 December 2019

author name string

M G Butler

1

1 reference

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7 December 2019

L Hedges

2

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7 December 2019

C L Hovis

3

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7 December 2019

publication date

1 November 1998

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7 December 2019

Clinical Genetics

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7 December 2019

54

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7 December 2019

385-393

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7 December 2019

5

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7 December 2019

The frequency of uniparental disomy in Prader-Willi syndrome. Implications for molecular diagnosis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/9842990

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prader-Willi syndrome: current understanding of cause and diagnosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/9842990

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The developing role of anthropologists in medical genetics: anthropometric assessment of the Prader-Labhart-Willi syndrome as an illustration

1 reference

https://pubmed.ncbi.nlm.nih.gov/9842990

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

RESTING METABOLIC RATE IN PRADER-WILLI SYNDROME

1 reference

https://pubmed.ncbi.nlm.nih.gov/9842990

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of Obesity in the Prader-Labhart-Willi Syndrome: Fatness Patterning

1 reference

https://pubmed.ncbi.nlm.nih.gov/9842990

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An anthropometric study of 38 individuals with Prader-Labhart-Willi syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/9842990

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/9842990

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prader-Willi syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/9842990

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Photoanthropometric study of craniofacial traits of individuals with Prader-Willi syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/9842990

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Overexpression of the obese (ob) gene in adipose tissue of human obese subjects

1 reference

https://pubmed.ncbi.nlm.nih.gov/9842990

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Increased obese mRNA expression in omental fat cells from massively obese humans

1 reference

https://pubmed.ncbi.nlm.nih.gov/9842990

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular characterization of two proximal deletion breakpoint regions in both Prader-Willi and Angelman syndrome patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/9842990

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Effects of the obese gene product on body weight regulation in ob/ob mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/9842990

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The minisatellite in the diabetes susceptibility locus IDDM2 regulates insulin transcription.

1 reference

https://pubmed.ncbi.nlm.nih.gov/9842990

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15.

1 reference

https://pubmed.ncbi.nlm.nih.gov/9842990

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Positional cloning of the mouse obese gene and its human homologue

1 reference

https://pubmed.ncbi.nlm.nih.gov/9842990

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Guidelines for overweight in adolescent preventive services: recommendations from an expert committee. The Expert Committee on Clinical Guidelines for Overweight in Adolescent Preventive Services

1 reference

https://pubmed.ncbi.nlm.nih.gov/9842990

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An association between the risk of cancer and mutations in the HRAS1 minisatellite locus.

1 reference

https://pubmed.ncbi.nlm.nih.gov/9842990

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genomic imprinting and candidate genes in the Prader-Willi and Angelman syndromes

1 reference

https://pubmed.ncbi.nlm.nih.gov/9842990

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Allelic variation of reporter gene activation by the HRAS1 minisatellite

1 reference

https://pubmed.ncbi.nlm.nih.gov/9842990

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prader-Willi syndrome: consensus diagnostic criteria.

1 reference

https://pubmed.ncbi.nlm.nih.gov/9842990

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification and expression cloning of a leptin receptor, OB-R

1 reference

https://pubmed.ncbi.nlm.nih.gov/9842990

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Absence of mutations in the human OB gene in obese/diabetic subjects

1 reference

https://pubmed.ncbi.nlm.nih.gov/9842990

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A 5-year-old white girl with Prader-Willi syndrome and a submicroscopic deletion of chromosome 15q11q13.

1 reference

https://pubmed.ncbi.nlm.nih.gov/9842990

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic variants of the human obesity (OB) gene: association with body mass index in young women, psychiatric symptoms, and interaction with the dopamine D2 receptor (DRD2) gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/9842990

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital leptin deficiency is associated with severe early-onset obesity in humans

1 reference

https://pubmed.ncbi.nlm.nih.gov/9842990

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Comparison of leptin protein levels in Prader-Willi syndrome and control individuals.

1 reference

https://pubmed.ncbi.nlm.nih.gov/9842990

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1111/J.1399-0004.1998.TB03751.X

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9842990%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9842990%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9842990%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

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