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K D Mathews

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Muscle & Nerve. Supplement|January 1, 1995
Mouse myodystrophy (myd) mutation: refined mapping in an interval flanked by homology with distal human 4qK D Mathews, K A Mills, H L Bailey, et al.
Journal of Neuropathology and Experimental Neurology|July 1, 1995
Phenotypic and pathologic evaluation of the myd mouse. A candidate model for facioscapulohumeral dystrophyK D Mathews, D Rapisarda, H L Bailey, et al.
Genomics|September 1, 1996
Genetic and physical mapping of a voltage-dependent chloride channel gene to human 4q32 and to mouse 8K A Mills, K D Mathews, T Scherpbier-Heddema, et al.
American Journal of Medical Genetics|December 1, 1989
Linkage localization of Börjeson-Forssman-Lehmann syndromeK D Mathews, H H Ardinger, D Y Nishimura, et al.
Pediatric Cardiology|July 2, 2005
Steroid therapy and cardiac function in Duchenne muscular dystrophyL W Markham, R L Spicer, P R Khoury, et al.
Neurology|January 12, 2011
Myoglobinuria and muscle pain are common in patients with limb-girdle muscular dystrophy 2IK D Mathews, C M Stephan, K Laubenthal, et al.
American Journal of Human Genetics|August 1, 1992
Linkage localization of facioscapulohumeral muscular dystrophy (FSHD) in 4q35K D Mathews, K A Mills, E P Bosch, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|June 1, 1997
The mouse homolog of FRG1, a candidate gene for FSHD, maps proximal to the myodystrophy mutation on chromosome 8P K Grewal, J C van Deutekom, K A Mills, et al.
American Journal of Human Genetics|August 1, 1992
Genetic and physical mapping on chromosome 4 narrows the localization of the gene for facioscapulohumeral muscular dystrophy (FSHD)K A Mills, K H Buetow, Y Xu, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|May 1, 1994
The DNA rearrangement associated with facioscapulohumeral muscular dystrophy involves a heterochromatin-associated repetitive element: implications for a role of chromatin structure in the pathogenesis of the diseaseS T Winokur, U Bengtsson, J Feddersen, et al.
Pageof 3

Showing results (11-20 of 22) with videos related to

Sort By:
Pageof 3
Muscle & Nerve. Supplement|January 1, 1995
Mouse myodystrophy (myd) mutation: refined mapping in an interval flanked by homology with distal human 4qK D Mathews, K A Mills, H L Bailey, et al.
Journal of Neuropathology and Experimental Neurology|July 1, 1995
Phenotypic and pathologic evaluation of the myd mouse. A candidate model for facioscapulohumeral dystrophyK D Mathews, D Rapisarda, H L Bailey, et al.
Genomics|September 1, 1996
Genetic and physical mapping of a voltage-dependent chloride channel gene to human 4q32 and to mouse 8K A Mills, K D Mathews, T Scherpbier-Heddema, et al.
American Journal of Medical Genetics|December 1, 1989
Linkage localization of Börjeson-Forssman-Lehmann syndromeK D Mathews, H H Ardinger, D Y Nishimura, et al.
Pediatric Cardiology|July 2, 2005
Steroid therapy and cardiac function in Duchenne muscular dystrophyL W Markham, R L Spicer, P R Khoury, et al.
Neurology|January 12, 2011
Myoglobinuria and muscle pain are common in patients with limb-girdle muscular dystrophy 2IK D Mathews, C M Stephan, K Laubenthal, et al.
American Journal of Human Genetics|August 1, 1992
Linkage localization of facioscapulohumeral muscular dystrophy (FSHD) in 4q35K D Mathews, K A Mills, E P Bosch, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|June 1, 1997
The mouse homolog of FRG1, a candidate gene for FSHD, maps proximal to the myodystrophy mutation on chromosome 8P K Grewal, J C van Deutekom, K A Mills, et al.
American Journal of Human Genetics|August 1, 1992
Genetic and physical mapping on chromosome 4 narrows the localization of the gene for facioscapulohumeral muscular dystrophy (FSHD)K A Mills, K H Buetow, Y Xu, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|May 1, 1994
The DNA rearrangement associated with facioscapulohumeral muscular dystrophy involves a heterochromatin-associated repetitive element: implications for a role of chromatin structure in the pathogenesis of the diseaseS T Winokur, U Bengtsson, J Feddersen, et al.
Pageof 3