K. Lawler

Type de document

Co-auteur

I.S. Farooqi

G. Strohbehn

M. Smith

M.C. Sadler

A. Reymond

V. Plagnol

N. Patel

K.K. Lo

Z. Kutalik

J.M. Keogh

J. Keogh

M. Jõeloo

J. Humphrey

A. Hokken-Koelega

E. Henning

R. Hanssen

H.V. Firth

S. Donze

L. Damen

S. Croizier

S.G. Bouret

R. Bounds

E.G. Bochukova

C. Auwerx

Date

Source

Serveur académique Lausannois (2)

Mot-clé

maladie (2) Persons (2) Obesity (2) Human beings (2) Expression (2) maladie (2) tissu (corporel) (1) spectacle (1) risque (1) association (1) analyse (1) énergie (1) biomarqueur (1) Deletion (1) Leptin (1) Causes (1) Control (1) Genes (1) Animal feeding (1) Rates (1) Usage (1) Social groups (1) Scarcity (1) Risk (1) RNA (1) Weight loss (1) Proteins (1) Prader-Willi syndrome (1) Power resources (1) Power (Mechanics) (1)

Documents écrit par K. Lawler (2) | parle de K. Lawler (0)

Chromosomal deletions on 16p11.2 encompassing SH2B1 are associated with accelerated metabolic disease.

R. Hanssen et al. (15 août 2023)

A Transcriptomic Signature of the Hypothalamic Response to Fasting and BDNF Deficiency in Prader-Willi Syndrome.

E.G. Bochukova et al. (2018)