Weight loss in obese children carrying the proopiomelanocortin R236G variant (Q47338322)

14 January 2018

title

Weight loss in obese children carrying the proopiomelanocortin R236G variant (English)

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N Santoro

1

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L Perrone

2

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G Cirillo

3

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P Raimondo

4

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A Amato

5

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F Coppola

6

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M Santarpia

7

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A D'Aniello

8

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E Miraglia Del Giudice

9

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publication date

1 March 2006

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Journal of Endocrinological Investigation

published in

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volume

29

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issue

3

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page(s)

226-230

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https://scigraph.springernature.com/pub.10.1007/bf03345544

exact match

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Leptin increases hypothalamic pro-opiomelanocortin mRNA expression in the rostral arcuate nucleus.

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Severe early-onset obesity, adrenal insufficiency and red hair pigmentation caused by POMC mutations in humans

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Systematic mutation screening of the pro-opiomelanocortin gene: identification of several genetic variants including three different insertions, one nonsense and two missense point mutations in probands of different weight extremes

21 January 2018

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A missense mutation disrupting a dibasic prohormone processing site in pro-opiomelanocortin (POMC) increases susceptibility to early-onset obesity through a novel molecular mechanism

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21 January 2018

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Central nervous system control of food intake

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12 December 2020

Body Mass Index variations: centiles from birth to 87 years

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12 December 2020

Molecular screening of the proopiomelanocortin (POMC ) gene in Italian obese children: report of three new mutations

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12 December 2020

Predicting basal metabolic rate, new standards and review of previous work

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12 December 2020

Genetics of body-weight regulation

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Molecular cloning, expression, and gene localization of a fourth melanocortin receptor

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Identification and functional analysis of novel human melanocortin-4 receptor variants

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Identifiers

DOI

10.1007/BF03345544

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14 January 2018

PubMed ID

16682835

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14 January 2018