|1.||Gourdon, Geneviève: 5 articles (10/2013 - 01/2004)|
|2.||Thornton, Charles A: 4 articles (02/2013 - 01/2007)|
|3.||Wieringa, Bé: 4 articles (01/2013 - 10/2004)|
|4.||Wansink, Derick G: 4 articles (01/2013 - 10/2004)|
|5.||Reddy, S: 4 articles (10/2005 - 06/2000)|
|6.||Mahadevan, Mani S: 3 articles (01/2014 - 05/2005)|
|7.||Puymirat, Jack: 3 articles (01/2012 - 05/2003)|
|8.||Furling, Denis: 3 articles (01/2012 - 03/2003)|
|9.||Yadava, Ramesh S: 2 articles (01/2014 - 09/2006)|
|10.||Kuntzer, Thierry: 2 articles (10/2013 - 08/2008)|
|1.||Myotonic Dystrophy (Dystrophia Myotonica)
10/01/1998 - "Recent studies have shown that the severity of the several clinical symptoms of myotonic dystrophy (DM) is closely related to the size of a CTG triplet repeat in the gene encoding myotonin protein kinase. "
07/01/1998 - "From our previous studies, myotonic dystrophy protein kinase: gene product of myotonic dystrophy is localized at the terminal cisternae of sarcoplasmic reticulum of human adult muscle. "
04/01/1995 - "Here we use muscle biopsies from classical adult-onset myotonic dystrophy patients to study the accumulation of transcripts from both the normal and expanded DM kinase genes in patient muscle, and compare the results to normal and myopathic controls. "
01/01/2014 - "Myotonic dystrophy type 1 (DM1) is caused by the expansion of an unstable CTG repeat located in the 3'-UTR of (DMPK) the DM protein kinase gene. "
10/01/2013 - "Myotonic dystrophy (DM1) is a multisystemic disease caused by an expansion of CTG repeats in the region of DMPK, the gene encoding DM protein kinase. "
|2.||Myotonic Disorders (Paramyotonia Congenita)
12/01/1999 - "Myotonic dystrophy is the most common myotonic disorder and genetic studies disclosed the presence of abnormal triplet repeat in the chromosome 19q13.1 and the gene product is known as myotonin protein kinase. "
12/01/1999 - "Proximal myotonic myopathy (PROMM) was first described in 1994 as a multisystem disorder with similarity to myotonic dystrophy (DM), but without the abnormal (CTG)n expansion in the DM protein kinase (DMPK) gene. "
07/08/1997 - "Expansion of a CTG trinucleotide repeat in the 3' untranslated region (UTR) of DMPK, the gene encoding myotonic dystrophy protein kinase, induces the dominantly inherited neuromuscular disorder myotonic dystrophy (DM). "
|3.||Muscular Dystrophies (Muscular Dystrophy)
06/01/2002 - "Myotonic muscular dystrophy (DM) is characterized by abnormal skeletal muscle Na channel gating and reduced levels of myotonic dystrophy protein kinase (DMPK). "
04/01/1997 - "It is quite important to know the exact localization and function of myotonin protein kinase (MtPK), identified as the gene product of myotonic dystrophy, the most prevalent disease with multisystem disorders among muscular dystrophies. "
07/28/2000 - "The genetic abnormality in myotonic muscular dystrophy, multiple CTG repeats lie upstream of a gene that encodes a novel protein kinase, myotonic dystrophy protein kinase (DMPK). "
05/01/1995 - "Since the myotonic muscular dystrophy gene encodes a product, human myotonin protein kinase, with structural similarity to protein kinases, we tested the idea that human myotonin protein kinase modulates skeletal muscle Na channels. "
01/15/2014 - "Myotonic dystrophy type 1 (DM1), the most common form of adult-onset muscular dystrophy, is caused by an expanded (CTG)n repeat in the 3' untranslated region of the DM protein kinase (DMPK) gene. "
|4.||Neuromuscular Diseases (Neuromuscular Disease)
04/16/2003 - "Dysfunction of the gene encoding DMPK (myotonic dystrophy protein kinase) has been implicated in the human neuromuscular disease myotonic dystrophy (DM1). "
09/01/2001 - "Myotonic dystrophy (DM), an autosomal dominant neuromuscular disease, is associated with expansion of a polymorphic (CTG)n repeat in the 3'-untranslated region of the DM protein kinase (DMPK) gene. "
11/15/1996 - "Myotonic dystrophy (DM) is an autosomal dominant neuromuscular disease that is associated with a (CTG)n repeat expansion in the 3'-untranslated region of the myotonin protein kinase (Mt-PK) gene. "
01/01/1995 - "Myotonic dystrophy (DM) is a dominant neuromuscular disease that results from an unstable CTG-repeat expansion in the 3' UTR of the myotonin kinase gene at 19q13.3. This repeat is normally polymorphic with a trimodal distribution reflecting 5-, 11-17-, and 19-30-repeat-length alleles. "
07/01/2008 - "Due to somatic instability, which has been shown previously in DM1, the myotonin protein kinase (DMPK) gene appears to act as a tumor suppressor. "
09/01/1999 - "Length of (CTG)n triplet repeats in myotonic dystrophy protein kinase gene (DMPK) was estimated in tumors, normal tissues of the same organs, muscles, and leukocytes from three myotonic dystrophy (DM) patients and a non-DM patient. "
09/01/1999 - "Elongation of (CTG)n repeats in myotonic dystrophy protein kinase gene in tumors associated with myotonic dystrophy patients."
08/01/1995 - "Drosophila warts--tumor suppressor and member of the myotonic dystrophy protein kinase family."
02/01/2004 - "Tissue and tumor mosaicism of the myotonin protein kinase gene trinucleotide repeat in a patient with multiple basal cell carcinomas associated with myotonic dystrophy."
|2.||3' Untranslated Regions (3' UTR)
|3.||Protein Kinases (Protein Kinase)
|4.||Messenger RNA (mRNA)
|6.||RNA (Ribonucleic Acid)
|10.||Carrier Proteins (Binding Protein)