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Chondromodulin 1 stabilizes the chondrocyte phenotype and inhibits endochondral ossification of porcine cartilage repair tissue

Klinger, P. et al.

Arthritis and rheumatism. VOL 63; NUMBER 9, ; 2011, 2721-2731 -- John Wiley & Sons, Ltd -- 2011

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Developing multidisciplinary clinics for neuromuscular care and research

Paganoni, S. et al.

Muscle & nerve. VOL 56; NUMBER 5, ; 2017, 848-858 -- John Wiley & Sons, Ltd

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Human dermal fibroblasts derived from oculodentodigital dysplasia patients suggest that patients may have wound-healing defects

Churko, J. M. et al.

Human mutation. VOL 32; NUMBER 4, ; 2011, 456-466 -- John Wiley & Sons, Ltd -- 2011

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Hypoxia-inducible factor 1a is involved in the prostaglandin metabolism of osteoarthritic cartilage through up-regulation of microsomal prostaglandin E synthase 1 in articular chondrocytes

Grimmer, C. et al.

Arthritis and rheumatism. VOL 56; NUMBER 12, ; 2007, 4084-4094 -- John Wiley & Sons, Ltd (pages 4084-4094) -- 2007

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Identification of genetic disparity between primary and metastatic melanoma in human patients

Swoboda, A. et al.

Genes, chromosomes and cancer. VOL 50; NUMBER 9, ; 2011, 680-688 -- John Wiley & Sons, Ltd -- 2011

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Natural history of infantile-onset spinal muscular atrophy

Kolb, S. J. et al.

Annals of neurology. VOL 82; NUMBER 6, ; 2017, 883-891 -- John Wiley & Sons, Ltd

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A new distal arthrogryposis syndrome characterized by plantar flexion contractures

Stevenson, D. A. et al.

American journal of medical genetics. Part A. VOL 140; NUMBER 24, ; 2006, 2797-2801 -- John Wiley & Sons, Ltd (pages 2797-2801) -- 2006

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Nonsense mutation-associated Becker muscular dystrophy: interplay between exon definition and splicing regulatory elements within the DMD gene

Flanigan, K. M. et al.

Human mutation. VOL 32; NUMBER 3, ; 2011, 299-308 -- John Wiley & Sons, Ltd -- 2011

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Nucleophosmin is recognized by a cytotoxic T cell line derived from a rectal carcinoma patient

Swoboda, R. K. et al.

International journal of cancer. VOL 127; NUMBER 5, ; 2010, 1124-1130 -- John Wiley & Sons, Ltd (pages 1124-1130) -- 2010

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Position of Glycine Substitutions in the Triple Helix of COL6A1, COL6A2, and COL6A3 is Correlated with Severity and Mode of Inheritance in Collagen VI Myopathies

Butterfield, R. J. et al.

Human mutation. VOL 34; NUMBER 11, ; 2013, 1558-1567 -- John Wiley & Sons, Ltd Part 11; (pages 1558-1567) -- 2013

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by this Author/Contributor:

  1. Swoboda, K. J.
  2. Gelse, K.
  3. Dunn, D. M.
  4. Swoboda, B.
  5. Hennig, F. F.

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