Lista de obras -

A Monoallelic Two-Hit Mechanism in PLCD1 Explains the Genetic Pathogenesis of Hereditary Trichilemmal Cyst Formation

scientific article published on 11 May 2019

ABHD5 Stimulates PNPLA1-mediated Omega-O-Acylceramide Biosynthesis Essential for a Functional Skin Permeability Barrier

scientific article published on 25 October 2018

APMAP interacts with lysyl oxidase-like proteins, and disruption of Apmap leads to beneficial visceral adipose tissue expansion

artículo científico publicado en 2017

ATGL-mediated fat catabolism regulates cardiac mitochondrial function via PPAR-α and PGC-1.

artículo científico publicado en 2011

Adipose triglyceride lipase plays a key role in the supply of the working muscle with fatty acids

artículo científico publicado en 2009

Correction: Mutations in CERS3 Cause Autosomal Recessive Congenital Ichthyosis in Humans

artículo científico publicado en 2013

Distinct roles of adipose triglyceride lipase and hormone-sensitive lipase in the catabolism of triacylglycerol estolides

artículo científico publicado en 2021

Epidermal overexpression of xenobiotic receptor PXR impairs the epidermal barrier and triggers Th2 immune response.

artículo científico publicado en 2017

Fasting-induced G0/G1 switch gene 2 and FGF21 expression in the liver are under regulation of adipose tissue derived fatty acids

artículo científico publicado en 2015

Fat in the skin: Triacylglycerol metabolism in keratinocytes and its role in the development of neutral lipid storage disease.

artículo científico publicado en 2011

Functional cardiac lipolysis in mice critically depends on comparative gene identification-58.

artículo científico publicado en 2013

G0/G1 Switch Gene 2 Regulates Cardiac Lipolysis.

artículo científico publicado en 2015

G0/G1 switch gene-2 regulates human adipocyte lipolysis by affecting activity and localization of adipose triglyceride lipase

artículo científico publicado en 2012

Increased tonic cannabinoid CB1R activity and brain region-specific desensitization of CB1R Gi/o signaling axis in mice with global genetic knockout of monoacylglycerol lipase

artículo científico publicado en 2015

Monoglyceride lipase deficiency causes desensitization of intestinal cannabinoid receptor type 1 and increased colonic μ-opioid receptor sensitivity

artículo científico publicado en 2015

Monoglyceride lipase deficiency in mice impairs lipolysis and attenuates diet-induced insulin resistance.

artículo científico publicado en 2011

Mutations in CERS3 cause autosomal recessive congenital ichthyosis in humans

artículo científico publicado en 2013

Mutations in Recessive Congenital Ichthyoses Illuminate the Origin and Functions of the Corneocyte Lipid Envelope

artículo científico publicado en 2018

PNPLA1 Deficiency in Mice and Humans Leads to a Defect in the Synthesis of Omega-O-Acylceramides.

artículo científico publicado en 2016

PNPLA1 mutations cause autosomal recessive congenital ichthyosis in golden retriever dogs and humans

artículo científico publicado en 2012

Sixteen novel mutations in PNPLA1 in patients with autosomal recessive congenital ichthyosis reveal the importance of an extended patatin domain in PNPLA1 that is essential for proper human skin barrier function

artículo científico publicado en 2017

Skin Barrier Development Depends on CGI-58 Protein Expression during Late-Stage Keratinocyte Differentiation

artículo científico publicado en 2016

The C-terminal Region of Human Adipose Triglyceride Lipase Affects Enzyme Activity and Lipid Droplet Binding

artículo científico publicado en 2008

The important role of epidermal triacylglycerol metabolism for maintenance of the skin permeability barrier function.

artículo científico

Lista de obras de

A Monoallelic Two-Hit Mechanism in PLCD1 Explains the Genetic Pathogenesis of Hereditary Trichilemmal Cyst Formation

ABHD5 Stimulates PNPLA1-mediated Omega-O-Acylceramide Biosynthesis Essential for a Functional Skin Permeability Barrier

APMAP interacts with lysyl oxidase-like proteins, and disruption of Apmap leads to beneficial visceral adipose tissue expansion

ATGL-mediated fat catabolism regulates cardiac mitochondrial function via PPAR-α and PGC-1.

Adipose triglyceride lipase plays a key role in the supply of the working muscle with fatty acids

Correction: Mutations in CERS3 Cause Autosomal Recessive Congenital Ichthyosis in Humans

Distinct roles of adipose triglyceride lipase and hormone-sensitive lipase in the catabolism of triacylglycerol estolides

Epidermal overexpression of xenobiotic receptor PXR impairs the epidermal barrier and triggers Th2 immune response.

Fasting-induced G0/G1 switch gene 2 and FGF21 expression in the liver are under regulation of adipose tissue derived fatty acids

Fat in the skin: Triacylglycerol metabolism in keratinocytes and its role in the development of neutral lipid storage disease.

Functional cardiac lipolysis in mice critically depends on comparative gene identification-58.

G0/G1 Switch Gene 2 Regulates Cardiac Lipolysis.

G0/G1 switch gene-2 regulates human adipocyte lipolysis by affecting activity and localization of adipose triglyceride lipase

Increased tonic cannabinoid CB1R activity and brain region-specific desensitization of CB1R Gi/o signaling axis in mice with global genetic knockout of monoacylglycerol lipase

Monoglyceride lipase deficiency causes desensitization of intestinal cannabinoid receptor type 1 and increased colonic μ-opioid receptor sensitivity

Monoglyceride lipase deficiency in mice impairs lipolysis and attenuates diet-induced insulin resistance.

Mutations in CERS3 cause autosomal recessive congenital ichthyosis in humans

Mutations in Recessive Congenital Ichthyoses Illuminate the Origin and Functions of the Corneocyte Lipid Envelope

PNPLA1 Deficiency in Mice and Humans Leads to a Defect in the Synthesis of Omega-O-Acylceramides.

PNPLA1 mutations cause autosomal recessive congenital ichthyosis in golden retriever dogs and humans

Sixteen novel mutations in PNPLA1 in patients with autosomal recessive congenital ichthyosis reveal the importance of an extended patatin domain in PNPLA1 that is essential for proper human skin barrier function

Skin Barrier Development Depends on CGI-58 Protein Expression during Late-Stage Keratinocyte Differentiation

The C-terminal Region of Human Adipose Triglyceride Lipase Affects Enzyme Activity and Lipid Droplet Binding

The important role of epidermal triacylglycerol metabolism for maintenance of the skin permeability barrier function.