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Tobias Willer

Showing results (1-10 of 32) with videos related to

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Glycobiology|May 21, 2008
POMT2, a key enzyme in Walker-Warburg syndrome: somatic sPOMT2, but not testis-specific tPOMT2, is crucial for mannosyltransferase activity in vivoMark Lommel, Tobias Willer, Sabine Strahl
Glycobiology|December 4, 2002
Characterization of POMT2, a novel member of the PMT protein O-mannosyltransferase family specifically localized to the acrosome of mammalian spermatidsTobias Willer, Werner Amselgruber, Rainer Deutzmann, et al.
Molecular Microbiology|June 14, 2005
Protein O-mannosylation is crucial for cell wall integrity, septation and viability in fission yeastTobias Willer, Martin Brandl, Matthias Sipiczki, et al.
Methods in Enzymology|September 7, 2010
POMT1 is essential for protein O-mannosylation in mammalsMark Lommel, Tobias Willer, Jesús Cruces, et al.
Current Opinion in Structural Biology|October 22, 2003
O-mannosyl glycans: from yeast to novel associations with human diseaseTobias Willer, M Carmen Valero, Widmar Tanner, et al.
Skeletal Muscle|January 9, 2025
Sarcolemma resilience and skeletal muscle health require O-mannosylation of dystroglycanJeffrey M Hord, Sarah Burns, Tobias Willer, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 17, 2008
Brain and eye malformations resembling Walker-Warburg syndrome are recapitulated in mice by dystroglycan deletion in the epiblastJakob S Satz, Rita Barresi, Madeleine Durbeej, et al.
Glycobiology|November 6, 2012
Xylosyl- and glucuronyltransferase functions of LARGE in α-dystroglycan modification are conserved in LARGE2Kei-ichiro Inamori, Yuji Hara, Tobias Willer, et al.
Neuromuscular Disorders : NMD|March 29, 2005
An autosomal recessive limb girdle muscular dystrophy (LGMD2) with mild mental retardation is allelic to Walker-Warburg syndrome (WWS) caused by a mutation in the POMT1 geneBurcu Balci, Gökhan Uyanik, Pervin Dincer, et al.
Neuromuscular Disorders : NMD|April 4, 2009
Further evidence of Fukutin mutations as a cause of childhood onset limb-girdle muscular dystrophy without mental retardationRebecca L Puckett, Steven A Moore, Thomas L Winder, et al.
Pageof 4

Showing results (1-10 of 32) with videos related to

Sort By:
Pageof 4
Glycobiology|May 21, 2008
POMT2, a key enzyme in Walker-Warburg syndrome: somatic sPOMT2, but not testis-specific tPOMT2, is crucial for mannosyltransferase activity in vivoMark Lommel, Tobias Willer, Sabine Strahl
Glycobiology|December 4, 2002
Characterization of POMT2, a novel member of the PMT protein O-mannosyltransferase family specifically localized to the acrosome of mammalian spermatidsTobias Willer, Werner Amselgruber, Rainer Deutzmann, et al.
Molecular Microbiology|June 14, 2005
Protein O-mannosylation is crucial for cell wall integrity, septation and viability in fission yeastTobias Willer, Martin Brandl, Matthias Sipiczki, et al.
Methods in Enzymology|September 7, 2010
POMT1 is essential for protein O-mannosylation in mammalsMark Lommel, Tobias Willer, Jesús Cruces, et al.
Current Opinion in Structural Biology|October 22, 2003
O-mannosyl glycans: from yeast to novel associations with human diseaseTobias Willer, M Carmen Valero, Widmar Tanner, et al.
Skeletal Muscle|January 9, 2025
Sarcolemma resilience and skeletal muscle health require O-mannosylation of dystroglycanJeffrey M Hord, Sarah Burns, Tobias Willer, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 17, 2008
Brain and eye malformations resembling Walker-Warburg syndrome are recapitulated in mice by dystroglycan deletion in the epiblastJakob S Satz, Rita Barresi, Madeleine Durbeej, et al.
Glycobiology|November 6, 2012
Xylosyl- and glucuronyltransferase functions of LARGE in α-dystroglycan modification are conserved in LARGE2Kei-ichiro Inamori, Yuji Hara, Tobias Willer, et al.
Neuromuscular Disorders : NMD|March 29, 2005
An autosomal recessive limb girdle muscular dystrophy (LGMD2) with mild mental retardation is allelic to Walker-Warburg syndrome (WWS) caused by a mutation in the POMT1 geneBurcu Balci, Gökhan Uyanik, Pervin Dincer, et al.
Neuromuscular Disorders : NMD|April 4, 2009
Further evidence of Fukutin mutations as a cause of childhood onset limb-girdle muscular dystrophy without mental retardationRebecca L Puckett, Steven A Moore, Thomas L Winder, et al.
Pageof 4