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J Nowak

Showing results (761-770 of 807) with videos related to

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Acta Neuropathologica Communications|February 19, 2020
Nebulin nemaline myopathy recapitulated in a compound heterozygous mouse model with both a missense and a nonsense mutation in NebJenni M Laitila, Elyshia L McNamara, Catherine D Wingate, et al.
Human Molecular Genetics|October 1, 1996
Positional cloning of a gene involved in hereditary multiple exostosesW Wuyts, W Van Hul, J Wauters, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|November 10, 2005
Molecular study of malignant gliomas treated with epidermal growth factor receptor inhibitors: tissue analysis from North American Brain Tumor Consortium Trials 01-03 and 00-01Andrew B Lassman, Michael R Rossi, Jeffrey J Raizer, et al.
Muscle & Nerve|June 3, 2020
Clinical features of LRP4/agrin-antibody-positive myasthenia gravis: A multicenter studyMichael H Rivner, Brandy M Quarles, Jin-Xiu Pan, et al.
Therapeutic Advances in Neurological Disorders|April 19, 2024
Long-term safety and efficacy of zilucoplan in patients with generalized myasthenia gravis: interim analysis of the RAISE-XT open-label extension studyJames F Howard, Saskia Bresch, Constantine Farmakidis, et al.
Nature Genetics|October 3, 1999
Mutations in the skeletal muscle alpha-actin gene in patients with actin myopathy and nemaline myopathyK J Nowak, D Wattanasirichaigoon, H H Goebel, et al.
American Journal of Human Genetics|May 31, 2011
Mutations in the N-terminal actin-binding domain of filamin C cause a distal myopathyRachael M Duff, Valerie Tay, Peter Hackman, et al.
Brain : a Journal of Neurology|February 5, 2013
K7del is a common TPM2 gene mutation associated with nemaline myopathy and raised myofibre calcium sensitivityNancy Mokbel, Biljana Ilkovski, Michaela Kreissl, et al.
Reproductive Health|December 1, 2020
Neonatal deaths in infants born weighing ≥ 2500 g in low and middle-income countriesSarah Saleem, Farnaz Naqvi, Elizabeth M McClure, et al.
Genomics|June 15, 1997
A 2.8-Mb clone contig of the multiple endocrine neoplasia type 1 (MEN1) region at 11q13S C Guru, S E Olufemi, P Manickam, et al.
Pageof 81

Showing results (761-770 of 807) with videos related to

Sort By:
Pageof 81
Acta Neuropathologica Communications|February 19, 2020
Nebulin nemaline myopathy recapitulated in a compound heterozygous mouse model with both a missense and a nonsense mutation in NebJenni M Laitila, Elyshia L McNamara, Catherine D Wingate, et al.
Human Molecular Genetics|October 1, 1996
Positional cloning of a gene involved in hereditary multiple exostosesW Wuyts, W Van Hul, J Wauters, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|November 10, 2005
Molecular study of malignant gliomas treated with epidermal growth factor receptor inhibitors: tissue analysis from North American Brain Tumor Consortium Trials 01-03 and 00-01Andrew B Lassman, Michael R Rossi, Jeffrey J Raizer, et al.
Muscle & Nerve|June 3, 2020
Clinical features of LRP4/agrin-antibody-positive myasthenia gravis: A multicenter studyMichael H Rivner, Brandy M Quarles, Jin-Xiu Pan, et al.
Therapeutic Advances in Neurological Disorders|April 19, 2024
Long-term safety and efficacy of zilucoplan in patients with generalized myasthenia gravis: interim analysis of the RAISE-XT open-label extension studyJames F Howard, Saskia Bresch, Constantine Farmakidis, et al.
Nature Genetics|October 3, 1999
Mutations in the skeletal muscle alpha-actin gene in patients with actin myopathy and nemaline myopathyK J Nowak, D Wattanasirichaigoon, H H Goebel, et al.
American Journal of Human Genetics|May 31, 2011
Mutations in the N-terminal actin-binding domain of filamin C cause a distal myopathyRachael M Duff, Valerie Tay, Peter Hackman, et al.
Brain : a Journal of Neurology|February 5, 2013
K7del is a common TPM2 gene mutation associated with nemaline myopathy and raised myofibre calcium sensitivityNancy Mokbel, Biljana Ilkovski, Michaela Kreissl, et al.
Reproductive Health|December 1, 2020
Neonatal deaths in infants born weighing ≥ 2500 g in low and middle-income countriesSarah Saleem, Farnaz Naqvi, Elizabeth M McClure, et al.
Genomics|June 15, 1997
A 2.8-Mb clone contig of the multiple endocrine neoplasia type 1 (MEN1) region at 11q13S C Guru, S E Olufemi, P Manickam, et al.
Pageof 81