Search Results - Laing, Nigel G.

Actinopathies and Myosinopathies by Goebel, Hans H., Laing, Nigel G.

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Pathophysiological concepts in the congenital myopathies: blurring the boundaries, sharpening the focus by Ravenscroft, Gianina, Laing, Nigel G., Bönnemann, Carsten G.

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Nemaline Myopathy-Related Skeletal Muscle α-Actin (ACTA1) Mutation, Asp286Gly, Prevents Proper Strong Myosin Binding and Triggers Muscle Weakness by Ochala, Julien, Ravenscroft, Gianina, Laing, Nigel G., Nowak, Kristen J.

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Recent advances in understanding congenital myopathies by Ravenscroft, Gianina, Bryson-Richardson, Robert J., Nowak, Kristen J., Laing, Nigel G.

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Molecular Diagnosis of Duchenne Muscular Dystrophy: Past, Present and Future in Relation to Implementing Therapies by Laing, Nigel G, Davis, Mark R, Bayley, Klair, Fletcher, Sue, Wilton, Steve D

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Clinical utility gene card for: Nemaline myopathy by Nowak, Kristen J, Davis, Mark R, Wallgren-Pettersson, Carina, Lamont, Phillipa J, Laing, Nigel G

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Clinical Utility Gene Card for: Becker muscular dystrophy by Coote, David, Davis, Mark R., Cabrera, Macarena, Needham, Merrilee, Laing, Nigel G., Nowak, Kristen J.

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CUGC for Duchenne muscular dystrophy (DMD) by Coote, David J., Davis, Mark R., Cabrera, Macarena, Needham, Merrilee, Laing, Nigel G., Nowak, Kristen J.

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Clinical Utility Gene Card for: autosomal dominant myotonia congenita (Thomsen Disease) by Coote, David J., Davis, Mark R., Cabrera, Macarena, Needham, Merrilee, Laing, Nigel G., Nowak, Kristen J.

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Improved CRISPR/Cas9 gene editing in primary human myoblasts using low confluency cultures on Matrigel by Goullée, Hayley, Taylor, Rhonda L., Forrest, Alistair R. R., Laing, Nigel G., Ravenscroft, Gianina, Clayton, Joshua S.

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The exon 55 deletion in the nebulin gene - one single founder mutation with world-wide occurrence by Lehtokari, Vilma-Lotta, Greenleaf, Rebecca S., DeChene, Elizabeth T., Kellinsalmi, Mutsumi, Pelin, Katarina, Laing, Nigel G., Beggs, Alan H., Wallgren-Pettersson, Carina

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Nemaline myopathy type 6: clinical and myopathological features by Olivé, Montse, Goldfarb, Lev G, Lee, Hee-Suk, Odgerel, Zagaa, Blokhin, Andre, Gonzalez-Mera, Laura, Moreno, Dolores, Laing, Nigel G, Sambuughin, Nyamkhishig

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Motor neuron diseases caused by a novel VRK1 variant – A genotype/phenotype study by Sedghi, Maryam, Moslemi, Ali‐Reza, Olive, Montse, Etemadifar, Masoud, Ansari, Behnaz, Nasiri, Jafar, Emrahi, Leila, Mianesaz, Hamid‐Reza, Laing, Nigel G., Tajsharghi, Homa

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Disease Severity and Thin Filament Regulation in M9R TPM3 Nemaline Myopathy by Ilkovski, Biljana, Mokbel, Nancy, Lewis, Raymond A., Walker, Kendall, Nowak, Kristen J., Domazetovska, Ana, Laing, Nigel G., Fowler, Velia M., North, Kathryn N., Cooper, Sandra T.

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Early-onset Parkinson disease caused by a mutation in CHCHD2 and mitochondrial dysfunction by Lee, Richard G., Sedghi, Maryam, Salari, Mehri, Shearwood, Anne-Marie J., Stentenbach, Maike, Kariminejad, Ariana, Goullee, Hayley, Rackham, Oliver, Laing, Nigel G., Tajsharghi, Homa, Filipovska, Aleksandra

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STRetch: detecting and discovering pathogenic short tandem repeat expansions by Dashnow, Harriet, Lek, Monkol, Phipson, Belinda, Halman, Andreas, Sadedin, Simon, Lonsdale, Andrew, Davis, Mark, Lamont, Phillipa, Clayton, Joshua S., Laing, Nigel G., MacArthur, Daniel G., Oshlack, Alicia

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High-resolution iris and retinal imaging in multisystemic smooth muscle dysfunction syndrome due to a novel Asn117Lys substitution in ACTA2: a case report by Mc Glacken-Byrne, Aisling B., Prentice, David, Roshandel, Danial, Brown, Michael R., Tuch, Philip, Yau, Kyle S.-Y., Sivadorai, Padma, Davis, Mark R., Laing, Nigel G., Chen, Fred K.

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Gene Expression Networks in the Murine Pulmonary Myocardium Provide Insight into the Pathobiology of Atrial Fibrillation by Boutilier, Jordan K., Taylor, Rhonda L., Mann, Tracy, McNamara, Elyshia, Hoffman, Gary J., Kenny, Jacob, Dilley, Rodney J., Henry, Peter, Morahan, Grant, Laing, Nigel G., Nowak, Kristen J.

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Nemaline Myopathy with Minicores Caused by Mutation of the CFL2 Gene Encoding the Skeletal Muscle Actin–Binding Protein, Cofilin-2 by Agrawal, Pankaj B., Greenleaf, Rebecca S., Tomczak, Kinga K., Lehtokari, Vilma-Lotta, Wallgren-Pettersson, Carina, Wallefeld, William, Laing, Nigel G., Darras, Basil T., Maciver, Sutherland K., Dormitzer, Philip R., Beggs, Alan H.

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Approach to the diagnosis of congenital myopathies by North, Kathryn N., Wang, Ching H., Clarke, Nigel, Jungbluth, Heinz, Vainzof, Mariz, Dowling, James J., Amburgey, Kimberly, Quijano-Roy, Susana, Beggs, Alan H., Sewry, Caroline, Laing, Nigel G., Bönnemann, Carsten G.

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