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Molecular diversity of diencephalic astrocytes reveals adult astrogenesis regulated by Smad4

The EMBO journal, 2021-11, Vol.40 (21), p.e107532-n/a

2021

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An Alternative Approach for the Synthesis of Sulfoquinovosyldiacylglycerol

Molecules (Basel, Switzerland), 2021-07, Vol.26 (14), p.4275

2021

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

Biochimica et biophysica acta. Molecular and cell biology of lipids, 2014-03, Vol.1841 (3), p.409-415

2014

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CRISPR-Cas12a for Highly Efficient and Marker-Free Targeted Integration in Human Pluripotent Stem Cells

International journal of molecular sciences, 2024-01, Vol.25 (2), p.985

2024

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

The Journal of biological chemistry, 2008-06, Vol.283 (25), p.17211-17220

2008

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Mutations in a new cytochrome P450 gene in lamellar ichthyosis type 3

Human molecular genetics, 2006-03, Vol.15 (5), p.767-776

2006

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DNA methylation profiling of the human major histocompatibility complex: a pilot study for the human epigenome project

PLoS biology, 2004-12, Vol.2 (12), p.e405

2004

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Mutations in ichthyin a new gene on chromosome 5q33 in a new form of autosomal recessive congenital ichthyosis

Human molecular genetics, 2004-10, Vol.13 (20), p.2473-2482

2004

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Development of a targeted HPLC-ESI-QqQ-MS/MS method for the quantification of sulfolipids from a cyanobacterium, selected leafy vegetables, and a microalgae species

Analytical and bioanalytical chemistry, 2021-03, Vol.413 (7), p.1941-1954

2021

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Formation of keto-type ceramides in palmoplantar keratoderma based on biallelic KDSR mutations in patients

Human molecular genetics, 2022-03, Vol.31 (7), p.1105-1114

2022

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Adult neural stem cell activation in mice is regulated by the day/night cycle and intracellular calcium dynamics

Cell, 2021-02, Vol.184 (3), p.709-722.e13

2021

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Mutation in ALOX12B likely cause of POI and also ichthyosis in a large Iranian pedigree

Molecular genetics and genomics : MGG, 2020-07, Vol.295 (4), p.1039-1053

2020

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Identification of SLURP-1 as an epidermal neuromodulator explains the clinical phenotype of Mal de Meleda

Human molecular genetics, 2003-11, Vol.12 (22), p.3017-3024

2003

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Mutations in the transporter ABCA12 are associated with lamellar ichthyosis type 2

Human molecular genetics, 2003-09, Vol.12 (18), p.2369-2378

2003

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Fine mapping of eight psoriasis susceptibility loci

European journal of human genetics : EJHG, 2015-06, Vol.23 (6), p.844-853

2015

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Lipoxygenase-3 (ALOXE3) and 12(R)-lipoxygenase (ALOX12B) are mutated in non-bullous congenital ichthyosiform erythroderma (NCIE) linked to chromosome 17p13.1

Human molecular genetics, 2002-01, Vol.11 (1), p.107-113

2002

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Symptomatic lipid storage in carriers for the PNPLA2 gene

European journal of human genetics : EJHG, 2013-08, Vol.21 (8), p.892-892

2013

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Genetic linkage of Meleda disease to chromosome 8qter

European journal of human genetics : EJHG, 1998-11, Vol.6 (6), p.542-547

1998

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Mapping of Papillon-Lefevre syndrome to the chromosome 11q14 region

European journal of human genetics : EJHG, 1997-05, Vol.5 (3), p.156-160

1997

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CDKN1B/p27 is localized in mitochondria and improves respiration-dependent processes in the cardiovascular system-New mode of action for caffeine

PLoS biology, 2018-06, Vol.16 (6), p.e2004408-e2004408

2018

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Proteases and cystic fibrosis

The international journal of biochemistry & cell biology, 2008-01, Vol.40 (6), p.1238-1245

2008

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Interaction of Substrates with γ-Secretase at the Level of Individual Transmembrane Helices—A Methodological Approach

International journal of molecular sciences, 2023-09, Vol.24 (18), p.14396

2023

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Mechanism of Signalling and Adaptation through the Rhodobacter sphaeroides Cytoplasmic Chemoreceptor Cluster

International journal of molecular sciences, 2019-10, Vol.20 (20), p.5095

2019

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The gel-forming polysaccharide of psyllium husk ( Plantago ovata Forsk)

Carbohydrate research, 2004-08, Vol.339 (11), p.2009-2017

2004

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Genomic amplification and oncogenic properties of the GASC1 histone demethylase gene in breast cancer

Oncogene, 2009-12, Vol.28 (50), p.4491-4500

2009

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Molecular diversity of diencephalic astrocytes reveals adult astrogenesis regulated by Smad4

An Alternative Approach for the Synthesis of Sulfoquinovosyldiacylglycerol

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

CRISPR-Cas12a for Highly Efficient and Marker-Free Targeted Integration in Human Pluripotent Stem Cells

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

Mutations in a new cytochrome P450 gene in lamellar ichthyosis type 3

DNA methylation profiling of the human major histocompatibility complex: a pilot study for the human epigenome project

Mutations in ichthyin a new gene on chromosome 5q33 in a new form of autosomal recessive congenital ichthyosis

Development of a targeted HPLC-ESI-QqQ-MS/MS method for the quantification of sulfolipids from a cyanobacterium, selected leafy vegetables, and a microalgae species

Formation of keto-type ceramides in palmoplantar keratoderma based on biallelic KDSR mutations in patients

Adult neural stem cell activation in mice is regulated by the day/night cycle and intracellular calcium dynamics

Mutation in ALOX12B likely cause of POI and also ichthyosis in a large Iranian pedigree

Identification of SLURP-1 as an epidermal neuromodulator explains the clinical phenotype of Mal de Meleda

Mutations in the transporter ABCA12 are associated with lamellar ichthyosis type 2

Fine mapping of eight psoriasis susceptibility loci

Lipoxygenase-3 (ALOXE3) and 12(R)-lipoxygenase (ALOX12B) are mutated in non-bullous congenital ichthyosiform erythroderma (NCIE) linked to chromosome 17p13.1

Symptomatic lipid storage in carriers for the PNPLA2 gene

Genetic linkage of Meleda disease to chromosome 8qter

Mapping of Papillon-Lefevre syndrome to the chromosome 11q14 region

CDKN1B/p27 is localized in mitochondria and improves respiration-dependent processes in the cardiovascular system-New mode of action for caffeine

Proteases and cystic fibrosis

Interaction of Substrates with γ-Secretase at the Level of Individual Transmembrane Helices—A Methodological Approach

Mechanism of Signalling and Adaptation through the Rhodobacter sphaeroides Cytoplasmic Chemoreceptor Cluster

The gel-forming polysaccharide of psyllium husk ( Plantago ovata Forsk)

Genomic amplification and oncogenic properties of the GASC1 histone demethylase gene in breast cancer

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