<p>Cerebellar abnormalities in H&E-stainedand cresyl violet-counterstained sections through the cerebellum of a representative wild-type control (left panels) and a <i>Atoh1<sup>trhl/trhl</sup></i>(right panels) mouse shown under increasing magnification from 5X to 63X (n = 3 per group).Cerebella from each genotype were examined. The cerebellum in wild type is well developed and foliated(<b>A</b>), but it is smooth(<b>B</b>) in <i>Atoh1<sup>trhl/trhl</sup></i>mice.The external granule layer (EGL)is indicated by the arrow in both middle panels. In (<b>D</b>) the EGL of the<i>Atoh1<sup>trhl/trhl</sup></i>mice is significantly underdeveloped as compared to (<b>C</b>).Under high magnification, the Purkinje cell layer (PCL), indicated by the sta...
<p><b>A</b>) Double immunostaining with CaBP (green) and PV (red) in a transverse section through th...
(A) Immunohistochemical localization of EFA6C in the wild-type mouse cerebellar cortex. Note the int...
Ts65Dn mice are a genetic model for Down syndrome. Among others, these mice have cerebellar patholog...
<p>Sagittal sections through the medial cerebellum of adult wild type (A, D), <i>Apoer2</i> (B, E) o...
<p><b>A)</b> Kluver-Barrera's stain was performed on <i>ts3</i> and WT cerebella. Number and morphol...
This paper examines the structure and cytoarchitecture of the cerebellum of the weaver mutant mouse ...
A new mutant mouse named Stumbler (stu) displays clinical features suggesting a cerebellar lesion. T...
<p>A–D. Sagittal sections of the vermis of <i>Rere</i><sup>om/eyes3</sup> mice and their wild-type l...
Purkinje cells are the primary processing units of the cerebellar cortex and display molecular heter...
<p><b>A)</b> Brain images acquired by micro-MRI (left and middle panels). Horizontal (left) and sagi...
<p><b>A)</b> Representative ultra-high voltage electron microscopy (UHVEM) images of Purkinje cell d...
The architectonic and hodologic organization of the reeler cerebellum has been studied by means of i...
<p>A and B. Nissl straining of sagital sections from control (A) and tg (B) mice. No observable diff...
<p>(A) Macromorphological comparison between brains of the Ctrl and cKO mice. (B, C) Weight of the w...
EXPERIMENTAL STUDY OF MECHANISMS OF NEURODEGENERATION IN DIFFERENT CONDITIONS - SUMMARY MUDr. Zdeňka...
<p><b>A</b>) Double immunostaining with CaBP (green) and PV (red) in a transverse section through th...
(A) Immunohistochemical localization of EFA6C in the wild-type mouse cerebellar cortex. Note the int...
Ts65Dn mice are a genetic model for Down syndrome. Among others, these mice have cerebellar patholog...
<p>Sagittal sections through the medial cerebellum of adult wild type (A, D), <i>Apoer2</i> (B, E) o...
<p><b>A)</b> Kluver-Barrera's stain was performed on <i>ts3</i> and WT cerebella. Number and morphol...
This paper examines the structure and cytoarchitecture of the cerebellum of the weaver mutant mouse ...
A new mutant mouse named Stumbler (stu) displays clinical features suggesting a cerebellar lesion. T...
<p>A–D. Sagittal sections of the vermis of <i>Rere</i><sup>om/eyes3</sup> mice and their wild-type l...
Purkinje cells are the primary processing units of the cerebellar cortex and display molecular heter...
<p><b>A)</b> Brain images acquired by micro-MRI (left and middle panels). Horizontal (left) and sagi...
<p><b>A)</b> Representative ultra-high voltage electron microscopy (UHVEM) images of Purkinje cell d...
The architectonic and hodologic organization of the reeler cerebellum has been studied by means of i...
<p>A and B. Nissl straining of sagital sections from control (A) and tg (B) mice. No observable diff...
<p>(A) Macromorphological comparison between brains of the Ctrl and cKO mice. (B, C) Weight of the w...
EXPERIMENTAL STUDY OF MECHANISMS OF NEURODEGENERATION IN DIFFERENT CONDITIONS - SUMMARY MUDr. Zdeňka...
<p><b>A</b>) Double immunostaining with CaBP (green) and PV (red) in a transverse section through th...
(A) Immunohistochemical localization of EFA6C in the wild-type mouse cerebellar cortex. Note the int...
Ts65Dn mice are a genetic model for Down syndrome. Among others, these mice have cerebellar patholog...