List of works - Renate Lüllmann-Rauch

A disintegrin and metalloprotease 10 (ADAM10) is a central regulator of murine liver tissue homeostasis

scientific article published on March 2016

Array-based gene discovery with three unrelated subjects shows SCARB2/LIMP-2 deficiency causes myoclonus epilepsy and glomerulosclerosis

scientific article

Arylsulfatase G inactivation causes loss of heparan sulfate 3-O-sulfatase activity and mucopolysaccharidosis in mice

scientific article

Ataxia is the major neuropathological finding in arylsulfatase G-deficient mice: similarities and dissimilarities to Sanfilippo disease (mucopolysaccharidosis type III).

scientific article

Cerebellar alterations and gait defects as therapeutic outcome measures for enzyme replacement therapy in α-mannosidosis

scientific article

Chronic enzyme replacement therapy ameliorates neuropathology in alpha-mannosidosis mice

scientific article

Deficiency of the tetraspanin CD63 associated with kidney pathology but normal lysosomal function

scientific article published on 15 December 2008

Disturbed cholesterol traffic but normal proteolytic function in LAMP-1/LAMP-2 double-deficient fibroblasts

scientific article

Efficacy of enzyme replacement therapy in alpha-mannosidosis mice: a preclinical animal study

scientific article

Enzyme replacement improves ataxic gait and central nervous system histopathology in a mouse model of metachromatic leukodystrophy

scientific article

Enzyme replacement improves nervous system pathology and function in a mouse model for metachromatic leukodystrophy

scientific article (publication date: May 2005)

Functional characterization of the lysosomal membrane protein TMEM192 in mice

scientific article published on 28 April 2017

Induction of tolerance to human arylsulfatase A in a mouse model of metachromatic leukodystrophy

scientific article published on September 2007

LIMP-2/LGP85 deficiency causes ureteric pelvic junction obstruction, deafness and peripheral neuropathy in mice

scientific article (publication date: 15 March 2003)

Lysosome associated membrane proteins maintain pancreatic acinar cell homeostasis: LAMP-2 deficient mice develop pancreatitis

scientific article

Molecular characterization and gene disruption of mouse lysosomal putative serine carboxypeptidase 1.

scientific article published in March 2009

Myozap Deficiency Promotes Adverse Cardiac Remodeling via Differential Regulation of Mitogen-activated Protein Kinase/Serum-response Factor and β-Catenin/GSK-3β Protein Signaling

scientific article published on 30 December 2015

RIP3, a kinase promoting necroptotic cell death, mediates adverse remodelling after myocardial infarction

scientific article published on 11 June 2014

Reversal of peripheral and central neural storage and ataxia after recombinant enzyme replacement therapy in alpha-mannosidosis mice

scientific article

Sulfatide storage in neurons causes hyperexcitability and axonal degeneration in a mouse model of metachromatic leukodystrophy.

scientific article

Telencephalic histopathology and changes in behavioural and neural plasticity in a murine model for metachromatic leukodystrophy

scientific article published in April 2011

The disintegrin/metalloproteinase Adam10 is essential for epidermal integrity and Notch-mediated signaling

scientific article published on February 2011

The intramembrane protease SPPL2A is critical for tooth enamel formation

scientific article published in July 2013

The intramembrane protease SPPL2a promotes B cell development and controls endosomal traffic by cleavage of the invariant chain

scientific article published on 24 December 2012

The intramembrane proteases signal Peptide peptidase-like 2a and 2b have distinct functions in vivo

scientific article published on 03 February 2014

List of works by Renate Lüllmann-Rauch

A disintegrin and metalloprotease 10 (ADAM10) is a central regulator of murine liver tissue homeostasis

Array-based gene discovery with three unrelated subjects shows SCARB2/LIMP-2 deficiency causes myoclonus epilepsy and glomerulosclerosis

Arylsulfatase G inactivation causes loss of heparan sulfate 3-O-sulfatase activity and mucopolysaccharidosis in mice

Ataxia is the major neuropathological finding in arylsulfatase G-deficient mice: similarities and dissimilarities to Sanfilippo disease (mucopolysaccharidosis type III).

Cerebellar alterations and gait defects as therapeutic outcome measures for enzyme replacement therapy in α-mannosidosis

Chronic enzyme replacement therapy ameliorates neuropathology in alpha-mannosidosis mice

Deficiency of the tetraspanin CD63 associated with kidney pathology but normal lysosomal function

Disturbed cholesterol traffic but normal proteolytic function in LAMP-1/LAMP-2 double-deficient fibroblasts

Efficacy of enzyme replacement therapy in alpha-mannosidosis mice: a preclinical animal study

Enzyme replacement improves ataxic gait and central nervous system histopathology in a mouse model of metachromatic leukodystrophy

Enzyme replacement improves nervous system pathology and function in a mouse model for metachromatic leukodystrophy

Functional characterization of the lysosomal membrane protein TMEM192 in mice

Induction of tolerance to human arylsulfatase A in a mouse model of metachromatic leukodystrophy

LIMP-2/LGP85 deficiency causes ureteric pelvic junction obstruction, deafness and peripheral neuropathy in mice

Lysosome associated membrane proteins maintain pancreatic acinar cell homeostasis: LAMP-2 deficient mice develop pancreatitis

Molecular characterization and gene disruption of mouse lysosomal putative serine carboxypeptidase 1.

Myozap Deficiency Promotes Adverse Cardiac Remodeling via Differential Regulation of Mitogen-activated Protein Kinase/Serum-response Factor and β-Catenin/GSK-3β Protein Signaling

RIP3, a kinase promoting necroptotic cell death, mediates adverse remodelling after myocardial infarction

Reversal of peripheral and central neural storage and ataxia after recombinant enzyme replacement therapy in alpha-mannosidosis mice

Sulfatide storage in neurons causes hyperexcitability and axonal degeneration in a mouse model of metachromatic leukodystrophy.

Telencephalic histopathology and changes in behavioural and neural plasticity in a murine model for metachromatic leukodystrophy

The disintegrin/metalloproteinase Adam10 is essential for epidermal integrity and Notch-mediated signaling

The intramembrane protease SPPL2A is critical for tooth enamel formation

The intramembrane protease SPPL2a promotes B cell development and controls endosomal traffic by cleavage of the invariant chain

The intramembrane proteases signal Peptide peptidase-like 2a and 2b have distinct functions in vivo