H. Büssow

发表

Formation of a normal epidermis supported by increased stability of keratins 5 and 14 in keratin 10 null mice.

J. Reichelt, C. Grund, T. Magin, 2001, Molecular biology of the cell.

Expression pattern and functional characterization of connexin29 in transgenic mice

C. Wessig, K. Willecke, A. Schober, 2006, Glia.

Functional expression of connexin57 in horizontal cells of the mouse retina

Timm Schubert, R. Weiler, T. Schubert, 2004, The European journal of neuroscience.

Keratin 5 knockout mice reveal plasticity of keratin expression in the corneal epithelium.

M. Hesse, K. Weber, T. Magin, 2006, European journal of cell biology.

Complete cytolysis and neonatal lethality in keratin 5 knockout mice reveal its fundamental role in skin integrity and in epidermolysis bullosa simplex.

T. Magin, H. Büssow, J. Kirfel, 2001, Molecular biology of the cell.

A dominant vimentin mutant upregulates Hsp70 and the activity of the ubiquitin-proteasome system, and causes posterior cataracts in transgenic mice

T. Magin, Martin Müller, H. Büssow, 2008, Journal of Cell Science.

Down-regulation of Polysialic Acid Is Required for Efficient Myelin Formation*

H. Büssow, V. Gieselmann, M. Eckhardt, 2007, Journal of Biological Chemistry.

The tapetal cell: A unique melanocyte in the tapetum lucidum cellulosum of the cat (Felis domestica L.)

H. Büssow, C. Hansson, H. Baumgarten, 1980, Anatomy and Embryology.

Galactosphingolipids and axono-glial interaction in myelin of the central nervous system

A. Bosio, W. Stoffel, H. Büssow, 1998, Cell and Tissue Research.

Missense mutations as a cause of metachromatic leukodystrophy

H. Büssow, V. Gieselmann, A. Marcão, 2005, The FEBS journal.

A spontaneously immortalized Schwann cell line to study the molecular aspects of metachromatic leukodystrophy

S. Franken, H. Büssow, V. Gieselmann, 2007, Journal of Neuroscience Methods.

Oligodendrocytes expressing exclusively the DM20 isoform of the proteolipid protein gene: Myelination and development

W. Stoffel, H. Büssow, Olaf Spörkel, 2002, Glia.

Exocytosis of storage material in a lysosomal disorder.

H. Büssow, V. Gieselmann, S. N. Fewou, 2005, Biochemical and biophysical research communications.

Alopecia and male infertility in oligotriche mutant mice are caused by a deletion on distal chromosome 9

J. Guénet, Yoshikazu Nakamura, I. Aubin, 2008, Mammalian Genome.

Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71rco12 and Krt71rco13

H. Fuchs, K. Koch, M. H. Angelis, 2006, Mammalian Genome.

Functional Integration of Embryonic Stem Cell-Derived Neurons In Vivo

Marius Wernig, Heinz Beck, Oliver Brüstle, 2004, The Journal of Neuroscience.

Schwann cell myelin ensheathing C.N.S. axons in the nerve fibre layer of the cat retina

H. Büssow, 1978, Journal of neurocytology.

Early Onset of Axonal Degeneration in Double (plp−/−mag−/−) and Hypomyelinosis in Triple (plp−/−mbp−/−mag−/−) Mutant Mice

W. Stoffel, H. Büssow, Thomas Uschkureit, 2000, The Journal of Neuroscience.

The astrocytes in the retina and optic nerve head of mammals: A special glia for the ganglion cell axons

H. Büssow, 2004, Cell and Tissue Research.

Connexin 47 (Cx47)-Deficient Mice with Enhanced Green Fluorescent Protein Reporter Gene Reveal Predominant Oligodendrocytic Expression of Cx47 and Display Vacuolized Myelin in the CNS

K. Wellershaus, J. Degen, K. Willecke, 2003, The Journal of Neuroscience.

Grey, a novel mutation in the murine Lyst gene, causes the beige phenotype by skipping of exon 25

H. Büssow, G. Cox, F. Runkel, 2006, Mammalian Genome.

Rumpshaker‐like proteolipid protein (PLP) ratio in a mouse model with unperturbed structural and functional integrity of the myelin sheath and axons in the central nervous system

W. Stoffel, H. Büssow, Olaf Spörkel, 2001, Glia.

Alopecia in a novel mouse model RCO3 is caused by mK6irs1 deficiency.

H. Fuchs, M. Augustin, M. Hrabě de Angelis, 2003, The Journal of investigative dermatology.

Functional analysis in vivo of the double mutant mouse deficient in both proteolipid protein (PLP) and myelin basic protein (MBP) in the central nervous system

W. Stoffel, H. Büssow, D. Boison, 1997, Cell and Tissue Research.

Early Onset of Axonal Degeneration in Double ( plp 2 / 2 mag 2 / 2 ) and Hypomyelinosis in Triple ( plp 2 / 2 mbp 2 / 2 mag 2 / 2 ) Mutant Mice

W. Stoffel, H. Büssow, Olaf Spörkel, 2000 .

Reversal of non‐hydroxy : α‐hydroxy galactosylceramide ratio and unstable myelin in transgenic mice overexpressing UDP‐galactose : ceramide galactosyltransferase

N. Schaeren-Wiemers, H. Büssow, V. Gieselmann, 2005, Journal of neurochemistry.

Absence of 2-Hydroxylated Sphingolipids Is Compatible with Normal Neural Development But Causes Late-Onset Axon and Myelin Sheath Degeneration

D. Hartmann, H. Büssow, V. Gieselmann, 2008, The Journal of Neuroscience.

[The wall structure of large arteries in birds. Investigations by light- and electron microscopy (author's transl)].

H. Büssow, 1973, Zeitschrift fur Zellforschung und mikroskopische Anatomie.

Oligodendrocyte‐specific ceramide galactosyltransferase (CGT) expression phenotypically rescues CGT‐deficient mice and demonstrates that CGT activity does not limit brain galactosylceramide level

H. Büssow, V. Gieselmann, M. Eckhardt, 2005, Glia.

Adhesive properties of proteolipid protein are responsible for the compaction of CNS myelin sheaths

W. Stoffel, D. D'urso, H. Büssow, 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

Nerve endings in the arteria centralis retinae

H. Büssow, 1974, Cell and Tissue Research.