<p>(a) Schematic diagram of MOGiCre x JunB<sup>f/f</sup> and c-Jun<sup>f/f</sup> (JunB<sup>Δol</sup>/Jun-c<sup>Δol</sup>) mice. (b) Genotyping PCR using genomic DNA derived from various peripheral organs and CNS regions from a JunB<sup>flox/flox</sup> (top) and c-Jun<sup>flox/flox</sup> (bottom) MOGiCre/+ mutant (JunB<sup>Δol</sup>/c-Jun<sup>Δol</sup>) and from a homozygous JunB<sup>flox/flox</sup>/c-Jun<sup>flox/flox</sup> MOGiCre-negative control (JunB<sup>f/f</sup>/c-Jun<sup>f/f</sup>). Li, liver; Ki, kidney, Spl, spleen; Hr, heart; Thy, thymus, Lu, lung; Ln, lymph node; Br, brain; Cb, cerebellum; Sc, spinal cord. (c) Western Blot analysis for JunB, c-Jun and vinculin (loading control) in protein lysates obtained from CNS spinal cord tis...
Transgenic mice carrying amyotrophic lateral sclerosis (ALS)-linked superoxide dismutase 1 (SOD1) mu...
<p>Western blot analysis of tissues from the hippocampus (HP), Cerebellum (Cb), and cortex (Cx) in B...
The aim of this project was to understand the molecular mechanisms underlying movement disorders an...
<p>(a) Southern blot analysis of genomic DNA from total heart, skeletal muscle and kidney extracts. ...
Oligodendrocytes, the myelin-forming glial cells of the central nervous system (CNS), are fundamenta...
<p>Saggital sections of E10.5 <i>Isl1</i><sup>Cre/+</sup><i>; mT/mG; Jun</i><sup>flox/+</sup> (<b>A<...
<p>(A) (Top panel) FluoroMyelin staining of the corpus callosum of <i>Npc1<sup>flox/−</sup>, CNP<sup...
Oligodendrocytes, the myelin-forming glial cells of the central nervous system (CNS),are fundamental...
The motor neuron degeneration 2 (mnd2) mice carry a point mutation of A to T nucleo-tide transversio...
The mouse mutation mnd2 provides an experimental model for studying human neuromuscular and neurodeg...
<p>(A) Western blots of myelin-specific proteins from brainstem, cerebral cortex and cerebellar homo...
<p>Genotyping for the conditional <i>Msh2</i> allele in genomic DNA extracted from striatum of <i>Ms...
The jimpy rumpshaker (jprsh) mutation is an amino acid substitution in exon 4 (Ile186[RIGHTWARDS ARR...
<p>A, D) Nucleotide sequences of Jun and Myc promoter region fragments (upper strands) and the corre...
<p>(A) Brains of 7-month-old female mice harboring aPKCλ flox/−; S1-cre (S1-cko) or flox/+ (Cont) we...
Transgenic mice carrying amyotrophic lateral sclerosis (ALS)-linked superoxide dismutase 1 (SOD1) mu...
<p>Western blot analysis of tissues from the hippocampus (HP), Cerebellum (Cb), and cortex (Cx) in B...
The aim of this project was to understand the molecular mechanisms underlying movement disorders an...
<p>(a) Southern blot analysis of genomic DNA from total heart, skeletal muscle and kidney extracts. ...
Oligodendrocytes, the myelin-forming glial cells of the central nervous system (CNS), are fundamenta...
<p>Saggital sections of E10.5 <i>Isl1</i><sup>Cre/+</sup><i>; mT/mG; Jun</i><sup>flox/+</sup> (<b>A<...
<p>(A) (Top panel) FluoroMyelin staining of the corpus callosum of <i>Npc1<sup>flox/−</sup>, CNP<sup...
Oligodendrocytes, the myelin-forming glial cells of the central nervous system (CNS),are fundamental...
The motor neuron degeneration 2 (mnd2) mice carry a point mutation of A to T nucleo-tide transversio...
The mouse mutation mnd2 provides an experimental model for studying human neuromuscular and neurodeg...
<p>(A) Western blots of myelin-specific proteins from brainstem, cerebral cortex and cerebellar homo...
<p>Genotyping for the conditional <i>Msh2</i> allele in genomic DNA extracted from striatum of <i>Ms...
The jimpy rumpshaker (jprsh) mutation is an amino acid substitution in exon 4 (Ile186[RIGHTWARDS ARR...
<p>A, D) Nucleotide sequences of Jun and Myc promoter region fragments (upper strands) and the corre...
<p>(A) Brains of 7-month-old female mice harboring aPKCλ flox/−; S1-cre (S1-cko) or flox/+ (Cont) we...
Transgenic mice carrying amyotrophic lateral sclerosis (ALS)-linked superoxide dismutase 1 (SOD1) mu...
<p>Western blot analysis of tissues from the hippocampus (HP), Cerebellum (Cb), and cortex (Cx) in B...
The aim of this project was to understand the molecular mechanisms underlying movement disorders an...