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Olayinka Raheem

Showing results (1-10 of 25) with videos related to

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Acta Neuropathologica|January 29, 2010
Novel myosin heavy chain immunohistochemical double staining developed for the routine diagnostic separation of I, IIA and IIX fibersOlayinka Raheem, Sanna Huovinen, Tiina Suominen, et al.
Brain : a Journal of Neurology|April 27, 2010
Human disease caused by loss of fast IIa myosin heavy chain due to recessive MYH2 mutationsHoma Tajsharghi, David Hilton-Jones, Olayinka Raheem, et al.
Plos One|March 22, 2016
Distinct Muscle Biopsy Findings in Genetically Defined Adult-Onset Motor Neuron DisordersManu Jokela, Sanna Huovinen, Olayinka Raheem, et al.
Acta Neuropathologica|March 15, 2006
Perinuclear leucine-rich repeats and immunoglobulin-like domain proteins (LRIG1-3) as prognostic indicators in astrocytic tumorsDongsheng Guo, Jonas Nilsson, Hannu Haapasalo, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|November 11, 2008
Cytoplasmic LRIG2 expression is associated with poor oligodendroglioma patient survivalCamilla Holmlund, Hannu Haapasalo, Wei Yi, et al.
Acta Neuropathologica Communications|February 6, 2016
Diagnostically important muscle pathology in DNAJB6 mutated LGMD1DSatu Sandell, Sanna Huovinen, Johanna Palmio, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 5, 2010
The enigma of 7q36 linked autosomal dominant limb girdle muscular dystrophySatu Sandell, Sanna Huovinen, Jaakko Sarparanta, et al.
Plos One|March 13, 2014
Gene expression profiling in tibial muscular dystrophy reveals unfolded protein response and altered autophagyMark Screen, Olayinka Raheem, Jeanette Holmlund-Hampf, et al.
Molecular Cancer Therapeutics|January 7, 2005
Characterization of a novel cell line established from a patient with Herceptin-resistant breast cancerMinna Tanner, Anita I Kapanen, Teemu Junttila, et al.
Neuromuscular Disorders : NMD|June 21, 2011
Distinct distal myopathy phenotype caused by VCP gene mutation in a Finnish familyJohanna Palmio, Satu Sandell, Tiina Suominen, et al.
Pageof 3

Showing results (1-10 of 25) with videos related to

Sort By:
Pageof 3
Acta Neuropathologica|January 29, 2010
Novel myosin heavy chain immunohistochemical double staining developed for the routine diagnostic separation of I, IIA and IIX fibersOlayinka Raheem, Sanna Huovinen, Tiina Suominen, et al.
Brain : a Journal of Neurology|April 27, 2010
Human disease caused by loss of fast IIa myosin heavy chain due to recessive MYH2 mutationsHoma Tajsharghi, David Hilton-Jones, Olayinka Raheem, et al.
Plos One|March 22, 2016
Distinct Muscle Biopsy Findings in Genetically Defined Adult-Onset Motor Neuron DisordersManu Jokela, Sanna Huovinen, Olayinka Raheem, et al.
Acta Neuropathologica|March 15, 2006
Perinuclear leucine-rich repeats and immunoglobulin-like domain proteins (LRIG1-3) as prognostic indicators in astrocytic tumorsDongsheng Guo, Jonas Nilsson, Hannu Haapasalo, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|November 11, 2008
Cytoplasmic LRIG2 expression is associated with poor oligodendroglioma patient survivalCamilla Holmlund, Hannu Haapasalo, Wei Yi, et al.
Acta Neuropathologica Communications|February 6, 2016
Diagnostically important muscle pathology in DNAJB6 mutated LGMD1DSatu Sandell, Sanna Huovinen, Johanna Palmio, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 5, 2010
The enigma of 7q36 linked autosomal dominant limb girdle muscular dystrophySatu Sandell, Sanna Huovinen, Jaakko Sarparanta, et al.
Plos One|March 13, 2014
Gene expression profiling in tibial muscular dystrophy reveals unfolded protein response and altered autophagyMark Screen, Olayinka Raheem, Jeanette Holmlund-Hampf, et al.
Molecular Cancer Therapeutics|January 7, 2005
Characterization of a novel cell line established from a patient with Herceptin-resistant breast cancerMinna Tanner, Anita I Kapanen, Teemu Junttila, et al.
Neuromuscular Disorders : NMD|June 21, 2011
Distinct distal myopathy phenotype caused by VCP gene mutation in a Finnish familyJohanna Palmio, Satu Sandell, Tiina Suominen, et al.
Pageof 3