Myotonic Dystrophy Type 2 Found in Two of Sixty-Three Persons Diagnosed as Having Fibromyalgia

Por Auvinen, Satu, Suominen, Tiina, Hannonen, Pekka, Bachinski, Linda L., Krahe, Ralf, Udd, Bjarne
Publicado em 2008

ALTERED MEF2 ISOFORMS IN MYOTONIC DYSTROPHY AND OTHER NEUROMUSCULAR DISORDERS

Por BACHINSKI, LINDA L., SIRITO, MARIO, BÖHME, MARIA, BAGGERLY, KEITH A., UDD, BJARNE, KRAHE, RALF
Publicado em 2010

Altered expression and splicing of Ca(2+) metabolism genes in myotonic dystrophies DM1 and DM2

Por Vihola, Anna, Sirito, Mario, Bachinski, Linda L., Raheem, Olayinka, Screen, Mark, Suominen, Tiina, Krahe, Ralf, Udd, Bjarne
Publicado em 2013

Population frequency of myotonic dystrophy: higher than expected frequency of myotonic dystrophy type 2 (DM2) mutation in Finland

Por Suominen, Tiina, Bachinski, Linda L, Auvinen, Satu, Hackman, Peter, Baggerly, Keith A, Angelini, Corrado, Peltonen, Leena, Krahe, Ralf, Udd, Bjarne
Publicado em 2011

MOLECULAR SIGNATURES OF METASTASIS IN HEAD AND NECK CANCER

Por Colella, Stefano, Richards, Kristy L., Bachinski, Linda L., Baggerly, Keith A., Tsavachidis, Spiridon, Lang, James C., Schuller, David E., Krahe, Ralf
Publicado em 2008

Tissue Doppler Imaging Consistently Detects Myocardial Abnormalities in Patients With Hypertrophic Cardiomyopathy and Provides a Novel Means for an Early Diagnosis Before and Indep...

Por Nagueh, Sherif F., Bachinski, Linda L., Meyer, Denise, Hill, Rita, Zoghbi, William A., Tam, James W., Quiñones, Miguel A., Roberts, Robert, Marian, A.J.
Publicado em 2001

Mutant (CCTG)n Expansion Causes Abnormal Expression of Zinc Finger Protein 9 (ZNF9) in Myotonic Dystrophy Type 2

Por Raheem, Olayinka, Olufemi, Shodimu-Emmanuel, Bachinski, Linda L., Vihola, Anna, Sirito, Mario, Holmlund-Hampf, Jeanette, Haapasalo, Hannu, Li, Yi-Ping, Udd, Bjarne, Krahe, Ralf
Publicado em 2010

The Locus of a Novel Gene Responsible for Arrhythmogenic Right-Ventricular Dysplasia Characterized by Early Onset and High Penetrance Maps to Chromosome 10p12-p14

Por Li, Duanxiang, Ahmad, Ferhaan, Gardner, Martin J., Weilbaecher, Donald, Hill, Rita, Karibe, Akihiko, Gonzalez, Oscar, Tapscott, Terry, Sharratt, Geoffrey P., Bachinski, Linda L., Roberts, Robert
Publicado em 2000

Global analysis of aberrant pre-mRNA splicing in glioblastoma using exon expression arrays

Por Cheung, Hannah C, Baggerly, Keith A, Tsavachidis, Spiridon, Bachinski, Linda L, Neubauer, Valerie L, Nixon, Tamara J, Aldape, Kenneth D, Cote, Gilbert J, Krahe, Ralf
Publicado em 2008

Effects of MDM2, MDM4 and TP53 Codon 72 Polymorphisms on Cancer Risk in a Cohort Study of Carriers of TP53 Germline Mutations

Por Fang, Shenying, Krahe, Ralf, Lozano, Guillermina, Han, Younghun, Chen, Wei, Post, Sean M., Zhang, Baili, Wilson, Charmaine D., Bachinski, Linda L., Strong, Louise C., Amos, Christopher I.
Publicado em 2010

Methylation of the Candidate Biomarker TCF21 Is Very Frequent Across A Spectrum of Early Stage Non-Small Cell Lung Cancers

Por Richards, Kristy L., Zhang, Baili, Sun, Menghong, Dong, Wenli, Churchill, Jennifer, Bachinski, Linda L., Wilson, Charmaine D., Baggerly, Keith A., Yin, Guosheng, Neil Hayes, D., Wistuba, Ignacio I., Krahe, Ralf
Publicado em 2010

Differences in aberrant expression and splicing of sarcomeric proteins in the myotonic dystrophies DM1 and DM2

Por Vihola, Anna, Bachinski, Linda L., Sirito, Mario, Olufemi, Shodimu-Emmanuel, Hajibashi, Shohrae, Baggerly, Keith A., Raheem, Olayinka, Haapasalo, Hannu, Suominen, Tiina, Holmlund-Hampf, Jeanette, Paetau, Anders, Cardani, Rosanna, Meola, Giovanni, Kalimo, Hannu, Edström, Lars, Krahe, Ralf, Udd, Bjarne
Publicado em 2010

Most expression and splicing changes in myotonic dystrophy type 1 and type 2 skeletal muscle are shared with other muscular dystrophies

Por Bachinski, Linda L., Baggerly, Keith A., Neubauer, Valerie L., Nixon, Tamara J., Raheem, Olayinka, Sirito, Mario, Unruh, Anna K., Zhang, Jiexin, Nagarajan, Lalitha, Timchenko, Lubov T., Bassez, Guillaume, Eymard, Bruno, Gamez, Josep, Ashizawa, Tetsuo, Mendell, Jerry R., Udd, Bjarne, Krahe, Ralf
Publicado em 2013

Confirmation of the Type 2 Myotonic Dystrophy (CCTG)(n) Expansion Mutation in Patients with Proximal Myotonic Myopathy/Proximal Myotonic Dystrophy of Different European Origins: A...

Por Bachinski, Linda L., Udd, Bjarne, Meola, Giovanni, Sansone, Valeria, Bassez, Guillaume, Eymard, Bruno, Thornton, Charles A., Moxley, Richard T., Harper, Peter S., Rogers, Mark T., Jurkat-Rott, Karin, Lehmann-Horn, Frank, Wieser, Thomas, Gamez, Josep, Navarro, Carmen, Bottani, Armand, Kohler, Andre, Shriver, Mark D., Sallinen, Riitta, Wessman, Maija, Zhang, Shanxiang, Wright, Fred A., Krahe, Ralf
Publicado em 2003