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High NOTCH1 mRNA Expression Is Associated with Better Survival in HNSCC

International journal of molecular sciences, 2018-03, Vol.19 (3), p.830

2018

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Comparing TIMP-1 and Hsp70 in Blood and Saliva as Potential Prognostic Markers in HNSCC

Biomedicines, 2022-12, Vol.10 (12), p.3225

2022

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Expression cartography of human tissues using self organizing maps

BMC bioinformatics, 2011-07, Vol.12 (1), p.306-306, Article 306

2011

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IKK2/NF‐κB signaling protects neurons after traumatic brain injury

The FASEB journal, 2018-04, Vol.32 (4), p.1916-1932

2018

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Cerebellar Hypoplasia in Mice Lacking Selenoprotein Biosynthesis in Neurons

Biological trace element research, 2014-05, Vol.158 (2), p.203-210

2014

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SAHA ameliorates the SMA phenotype in two mouse models for spinal muscular atrophy

Human molecular genetics, 2010-04, Vol.19 (8), p.1492-1506

2010

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Plastin 3 ameliorates spinal muscular atrophy via delayed axon pruning and improves neuromuscular junction functionality

Human molecular genetics, 2013-04, Vol.22 (7), p.1328-1347

2013

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The Role of Microbiota in Liver Transplantation and Liver Transplantation-Related Biliary Complications

International journal of molecular sciences, 2023-03, Vol.24 (5), p.4841

2023

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A reliable transcriptomic risk-score applicable to formalin-fixed paraffin-embedded biopsies improves outcome prediction in localized prostate cancer

Molecular medicine (Cambridge, Mass.), 2024-02, Vol.30 (1), p.19-19, Article 19

2024

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Metabolic Role of Autophagy in the Pathogenesis and Development of NAFLD

Metabolites, 2023-01, Vol.13 (1), p.101

2023

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In vitro and ex vivo evaluation of second‐generation histone deacetylase inhibitors for the treatment of spinal muscular atrophy

Journal of neurochemistry, 2006-07, Vol.98 (1), p.193-202

2006

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SMN regulates axonal local translation via miR-183/mTOR pathway

Human molecular genetics, 2014-12, Vol.23 (23), p.6318-6331

2014

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Novel insights into SMALED2: BICD2 mutations increase microtubule stability and cause defects in axonal and NMJ development

Human molecular genetics, 2018-05, Vol.27 (10), p.1772-1784

2018

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Phenotypic extremes of BICD2-opathies: from lethal, congenital muscular atrophy with arthrogryposis to asymptomatic with subclinical features

European journal of human genetics : EJHG, 2017-09, Vol.25 (9), p.1040-1048

2017

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IKK mediates ischemia-induced neuronal death

Nature medicine, 2005-12, Vol.11 (12), p.1322-1329

2005

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NF-κB is activated and promotes cell death in focal cerebral ischemia

Nature medicine, 1999-05, Vol.5 (5), p.554-559

1999

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LBH589 induces up to 10-fold SMN protein levels by several independent mechanisms and is effective even in cells from SMA patients non-responsive to valproate

Human molecular genetics, 2009-10, Vol.18 (19), p.3645-3658

2009

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Authentication of Primary Murine Cell Lines by a Microfluidics-Based Lab-On-Chip System

Biomedicines, 2020-12, Vol.8 (12), p.590

2020

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Severe SMA mice show organ impairment that cannot be rescued by therapy with the HDACi JNJ-26481585

European journal of human genetics : EJHG, 2013-06, Vol.21 (6), p.643-652

2013

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Reversible molecular pathology of skeletal muscle in spinal muscular atrophy

Human molecular genetics, 2011-11, Vol.20 (22), p.4334-4344

2011

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Plastin 3 is upregulated in iPSC-derived motoneurons from asymptomatic SMN1-deleted individuals

Cellular and molecular life sciences : CMLS, 2016-05, Vol.73 (10), p.2089-2104

2016

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Survival motor neuron gene 2 silencing by DNA methylation correlates with spinal muscular atrophy disease severity and can be bypassed by histone deacetylase inhibition

Human molecular genetics, 2009-01, Vol.18 (2), p.304-317

2009

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Deficiency of the splicing factor Sfrs10 results in early embryonic lethality in mice and has no impact on full-length SMN/Smn splicing

Human molecular genetics, 2010-06, Vol.19 (11), p.2154-2167

2010

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Lumazine proteins from photobacteria: localization of the single ligand binding site to the N-terminal domain

Biological chemistry, 2007-12, Vol.388 (12), p.1313-1323

2007

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High NOTCH1 mRNA Expression Is Associated with Better Survival in HNSCC

Comparing TIMP-1 and Hsp70 in Blood and Saliva as Potential Prognostic Markers in HNSCC

Expression cartography of human tissues using self organizing maps

IKK2/NF‐κB signaling protects neurons after traumatic brain injury

Cerebellar Hypoplasia in Mice Lacking Selenoprotein Biosynthesis in Neurons

SAHA ameliorates the SMA phenotype in two mouse models for spinal muscular atrophy

Plastin 3 ameliorates spinal muscular atrophy via delayed axon pruning and improves neuromuscular junction functionality

The Role of Microbiota in Liver Transplantation and Liver Transplantation-Related Biliary Complications

A reliable transcriptomic risk-score applicable to formalin-fixed paraffin-embedded biopsies improves outcome prediction in localized prostate cancer

Metabolic Role of Autophagy in the Pathogenesis and Development of NAFLD

In vitro and ex vivo evaluation of second‐generation histone deacetylase inhibitors for the treatment of spinal muscular atrophy

SMN regulates axonal local translation via miR-183/mTOR pathway

Novel insights into SMALED2: BICD2 mutations increase microtubule stability and cause defects in axonal and NMJ development

Phenotypic extremes of BICD2-opathies: from lethal, congenital muscular atrophy with arthrogryposis to asymptomatic with subclinical features

IKK mediates ischemia-induced neuronal death

NF-κB is activated and promotes cell death in focal cerebral ischemia

LBH589 induces up to 10-fold SMN protein levels by several independent mechanisms and is effective even in cells from SMA patients non-responsive to valproate

Authentication of Primary Murine Cell Lines by a Microfluidics-Based Lab-On-Chip System

Severe SMA mice show organ impairment that cannot be rescued by therapy with the HDACi JNJ-26481585

Reversible molecular pathology of skeletal muscle in spinal muscular atrophy

Plastin 3 is upregulated in iPSC-derived motoneurons from asymptomatic SMN1-deleted individuals

Survival motor neuron gene 2 silencing by DNA methylation correlates with spinal muscular atrophy disease severity and can be bypassed by histone deacetylase inhibition

Deficiency of the splicing factor Sfrs10 results in early embryonic lethality in mice and has no impact on full-length SMN/Smn splicing

Lumazine proteins from photobacteria: localization of the single ligand binding site to the N-terminal domain

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