T. Schmitt-John

发表

The wobbler mouse, an ALS animal model

J. Moser, P. Bigini, T. Schmitt-John, 2013, Molecular Genetics and Genomics.

VPS54 and the wobbler mouse

T. Schmitt-John, T. Schmitt‐John, 2015, Front. Neurosci..

α-Crystallins are involved in specific interactions with the murine γD/E/F-crystallin-encoding gene

T. Werner, J. Graw, T. Schmitt-John, 1994 .

Inflammation and neuronal death in the motor cortex of the wobbler mouse, an ALS animal model

C. Theiss, T. Schmitt-John, B. Brand-Saberi, 2015, Journal of Neuroinflammation.

Mutation of Vps54 causes motor neuron disease and defective spermiogenesis in the wobbler mouse

A. Lengeling, M. Meisler, H. Jockusch, 2005, Nature Genetics.

Intricate effects of primary motor neuronopathy on contractile proteins and metabolic muscle enzymes as revealed by label-free mass spectrometry

M. Henry, P. Meleady, M. Clynes, 2014, Bioscience reports.

Assignment1 of homologous genes, Peli1/PELI1 and Peli2/PELI2, for the Pelle adaptor protein Pellino to mouse chromosomes 11 and 14 and human chromosomes 2p13.3 and 14q21, respectively, by physical and radiation hybrid mapping

H. Jockusch, T. Schmitt-John, K. Resch, 2001, Cytogenetic and Genome Research.

Spatiotemporal progression of neurodegeneration and glia activation in the wobbler neuropathy of the mouse.

H. Jockusch, T. Schmitt-John, J. W. Bartsch, 1999, Neuroreport.

The Spatiotemporal Pattern of Degeneration in the Cerebellum of the Wobbler Mouse

C. Theiss, T. Schmitt-John, Veronika Matschke, 2016, Journal of neuropathology and experimental neurology.

Excitatory-inhibitory imbalance in the brain of the wobbler mouse model of amyotrophic lateral sclerosis substantiated by riluzole and diazepam

T. Schmitt-John, C. Lundbye, M. M. Holm, 2017, Neuroscience Letters.

Endosomal accumulation of APP in wobbler motor neurons reflects impaired vesicle trafficking: Implications for human motor neuron disease

C. Shaw, C. Troakes, P. Heimann, 2011, BMC Neuroscience.

Cat3vl and Cat3vao cataract mutations on mouse chromosome 10: phenotypic characterization, linkage studies and analysis of candidate genes

J. Graw, T. Schmitt-John, T. Immervoll, 1997, Molecular and General Genetics MGG.

Molecular analysis of two new Steel mutations in mice shows a transversion or an insertion

J. Graw, T. Schmitt-John, W. Pretsch, 1996, Mammalian Genome.

Genetic modifiers that aggravate the neurological phenotype of the wobbler mouse

M. Augustin, H. Jockusch, T. Schmitt-John, 2002, Neuroreport.

Assignment of homologous genes, Peli1/PELI1 and Peli2/PELI2, for the Pelle adaptor protein Pellino to mouse chromosomes 11 and 14 and human chromosomes 2p13.3 and 14q21, respectively, by physical and radiation hybrid mapping.

H. Jockusch, T. Schmitt-John, K. Resch, 2001, Cytogenetics and cell genetics.

Identification of Cis-regulatory elements in the mouse Pax9/Nkx2-9 genomic region: implication for evolutionary conserved synteny.

Kuniya Abe, K. Abe, K. Yamamura, 2003, Genetics.

The wobbler mouse, an ALS animal model

J. Moser, P. Bigini, T. Schmitt-John, 2013, Molecular Genetics and Genomics.

Mild phenotype in two unrelated patients with a partial deletion of 21q22.2‐q22.3 defined by FISH and molecular studies

J. Horst, I. Kennerknecht, J. Wirth, 2004, American journal of medical genetics. Part A.

Reduced GABAergic inhibition explains cortical hyperexcitability in the wobbler mouse model of ALS.

M. Lauritzen, K. Jensen, J. Moser, 2011, Cerebral cortex.

Genomic sequences of murine γB- and γC-crystallm-encoding genes: promoter analysis and complete evolutionary pattern of mouse, rat and human γ-crystallins

T. Werner, J. Graw, T. Schmitt-John, 1993 .

Characterization of a neuregulin-1 gene promoter: positive regulation of type I isoforms by NF-kappaB.

C. Kaltschmidt, T. Frensing, T. Schmitt-John, 2008, Biochimica et biophysica acta.

Conservation of the 3′‐untranslated region of the Rab1a gene in amniote vertebrates: exceptional structure in marsupials and possible role for posttranscriptional regulation

D. Evers, H. Jockusch, D. Eberhard, 2000, FEBS letters.

Vaccinia Virus Uses Retromer-Independent Cellular Retrograde Transport Pathways To Facilitate the Wrapping of Intracellular Mature Virions during Virus Morphogenesis

Tali Pechenick Jowers, I. Haga, P. Beard, 2016, Journal of Virology.

The Wobbler Mouse Model of Amyotrophic Lateral Sclerosis (ALS) Displays Hippocampal Hyperexcitability, and Reduced Number of Interneurons, but No Presynaptic Vesicle Release Impairments

M. Jensen, K. Jensen, J. Moser, 2013, PloS one.

Promoter constructions for efficient secretion expression in Streptomyces lividans

J. Engels, T. Schmitt-John, T. Schmitt‐John, 2004, Applied Microbiology and Biotechnology.

Close linkage of the dominant cataract mutations (Cat-2) with Idh-1 and cryge on mouse chromosome 1.

M. Lyon, J. Graw, T. Schmitt-John, 1994, Genomics.

Efficacy of Plasma-Treated Water against Salmonella Typhimurium: Antibacterial Activity, Inhibition of Invasion, and Biofilm Disruption

T. Schmitt-John, A. McWhorter, A. Abdo, 2023, Antibiotics.

Comparative transcription map of the wobbler critical region on mouse chromosome 11 and the homologous region on human chromosome 2p13-14

M. Platzer, H. Jockusch, T. Schmitt-John, 2002, BMC Genetics.

Morphological Studies of Wobbler Mouse Dorsal Root Ganglia Show Neurofilamental Disorders

C. Theiss, T. Schmitt-John, B. Brand-Saberi, 2017 .

Implementation of a manual for working with wobbler mice and criteria for discontinuation of the experiment.

C. Theiss, T. Schmitt-John, B. Brand-Saberi, 2015, Annals of anatomy = Anatomischer Anzeiger : official organ of the Anatomische Gesellschaft.

Pathoproteomics of testicular tissue deficient in the GARP component VPS54: The wobbler mouse model of globozoospermia

Lisa Staunton, H. Jockusch, A. Holland, 2014, Proteomics.

Homology between human Chromosome 2p13.3 and the wobbler critical region on mouse Chromosome 11: comparative high-resolution mapping of STS and EST loci on YAC/BAC contigs

A. Lengeling, H. Jockusch, K. Baer, 1998, Mammalian Genome.

Neuro-muscular function in the wobbler murine model of primary motor neuronopathy

A. Riisager, T. Schmitt-John, T. Pedersen, 2013, Experimental Neurology.

Comparison of pre- and post-implantation development following the application of three artificial activating stimuli in a mouse model with round-headed sperm cells deficient for oocyte activation.

B. Heindryckx, S. Lierman, P. De Sutter, 2013, Human reproduction.

Reduced fertilization after ICSI and abnormal phospholipase C zeta presence in spermatozoa from the wobbler mouse.

P. De Sutter, R. Soleimani, K. Coward, 2010, Reproductive biomedicine online.

Isolation and characterization of the novel popeye gene family expressed in skeletal muscle and heart.

H. Arnold, H. Jockusch, T. Schmitt-John, 2000, Developmental biology.

Loss of Vps54 Function Leads to Vesicle Traffic Impairment, Protein Mis-Sorting and Embryonic Lethality

E. Füchtbauer, A. Füchtbauer, P. Karlsson, 2013, International journal of molecular sciences.

P 206 CAT3, new cataract gene on mouse chromosome 10: Linkage studies and phenotypic characterization

J. Graw, T. Schmitt-John, J. Löster, 1995, Vision Research.