Search research articles
Contact Us
Filters
Showing results (31-40 of 69) with videos related to
Page
of 7
Sort By:
The American Journal of Pathology
|
August 10, 2014
IL-10, IL-4, and STAT6 promote an M2 milieu required for termination of P0(106-125)-induced murine experimental autoimmune neuritis
Anna Brunn, Mirna Mihelcic, Mariana Carstov, et al.
Journal of Neuropathology and Experimental Neurology
|
April 9, 2014
Costimulatory molecule CD40 is essential for myelin protein 0 peptide 106-125-induced experimental autoimmune neuritis in mice
Anna Brunn, Olaf Utermöhlen, Mirna Mihelcic, et al.
Acta Neuropathologica Communications
|
December 20, 2019
Bi-allelic mutations in uncoordinated mutant number-45 myosin chaperone B are a cause for congenital myopathy
Hormos Salimi Dafsari, Nur Mehpare Kocaturk, Hülya-Sevcan Daimagüler, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
July 31, 2018
Long term history of a congenital core-rod myopathy with compound heterozygous mutations in the Nebulin gene
Gilbert Wunderlich, Anna Brunn, Hülya-Sevcan Daimagüler, et al.
Haematologica
|
March 21, 2020
The process of somatic hypermutation increases polyreactivity for central nervous system antigens in primary central nervous system lymphoma
Manuel Montesinos-Rongen, Monica Terrao, Caroline May, et al.
European Journal of Immunology
|
January 23, 2019
TLR signals license CD8 T cells to destroy oligodendrocytes expressing an antigen shared with a Listeria pathogen
Monica Sánchez-Ruiz, Noelle Katherine Polakos, Tobias Blau, et al.
Molecular Imaging
|
February 5, 2010
Patient-tailored, imaging-guided, long-term temozolomide chemotherapy in patients with glioblastoma
Norbert Galldiks, Lutz W Kracht, Lothar Burghaus, et al.
Plos One
|
March 16, 2018
Distinct transcriptomic changes in E14.5 mouse skeletal muscle lacking RYR1 or Cav1.1 converge at E18.5
Dilyana Filipova, Margit Henry, Tamara Rotshteyn, et al.
The EMBO Journal
|
April 5, 2019
OTUB1 inhibits CNS autoimmunity by preventing IFN-γ-induced hyperactivation of astrocytes
Xu Wang, Floriana Mulas, Wenjing Yi, et al.
International Journal of Molecular Sciences
|
April 6, 2018
Dabrafenib Treatment in a Patient with an Epithelioid Glioblastoma and BRAF V600E Mutation
Garry Ceccon, Jan-Michael Werner, Veronika Dunkl, et al.
Page
of 7
Search research articles
Search
Showing results (31-40 of 69) with videos related to
Sort By:
Page
of 7
The American Journal of Pathology
|
August 10, 2014
IL-10, IL-4, and STAT6 promote an M2 milieu required for termination of P0(106-125)-induced murine experimental autoimmune neuritis
Anna Brunn, Mirna Mihelcic, Mariana Carstov, et al.
Journal of Neuropathology and Experimental Neurology
|
April 9, 2014
Costimulatory molecule CD40 is essential for myelin protein 0 peptide 106-125-induced experimental autoimmune neuritis in mice
Anna Brunn, Olaf Utermöhlen, Mirna Mihelcic, et al.
Acta Neuropathologica Communications
|
December 20, 2019
Bi-allelic mutations in uncoordinated mutant number-45 myosin chaperone B are a cause for congenital myopathy
Hormos Salimi Dafsari, Nur Mehpare Kocaturk, Hülya-Sevcan Daimagüler, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
July 31, 2018
Long term history of a congenital core-rod myopathy with compound heterozygous mutations in the Nebulin gene
Gilbert Wunderlich, Anna Brunn, Hülya-Sevcan Daimagüler, et al.
Haematologica
|
March 21, 2020
The process of somatic hypermutation increases polyreactivity for central nervous system antigens in primary central nervous system lymphoma
Manuel Montesinos-Rongen, Monica Terrao, Caroline May, et al.
European Journal of Immunology
|
January 23, 2019
TLR signals license CD8 T cells to destroy oligodendrocytes expressing an antigen shared with a Listeria pathogen
Monica Sánchez-Ruiz, Noelle Katherine Polakos, Tobias Blau, et al.
Molecular Imaging
|
February 5, 2010
Patient-tailored, imaging-guided, long-term temozolomide chemotherapy in patients with glioblastoma
Norbert Galldiks, Lutz W Kracht, Lothar Burghaus, et al.
Plos One
|
March 16, 2018
Distinct transcriptomic changes in E14.5 mouse skeletal muscle lacking RYR1 or Cav1.1 converge at E18.5
Dilyana Filipova, Margit Henry, Tamara Rotshteyn, et al.
The EMBO Journal
|
April 5, 2019
OTUB1 inhibits CNS autoimmunity by preventing IFN-γ-induced hyperactivation of astrocytes
Xu Wang, Floriana Mulas, Wenjing Yi, et al.
International Journal of Molecular Sciences
|
April 6, 2018
Dabrafenib Treatment in a Patient with an Epithelioid Glioblastoma and BRAF V600E Mutation
Garry Ceccon, Jan-Michael Werner, Veronika Dunkl, et al.
Page
of 7