Müller CR - Search Results

1

Distribution of emerin during the cell cycle.

Dabauvalle MC, Müller E, Ewald A, Kress W, Krohne G, Müller CR. Dabauvalle MC, et al. Among authors: muller cr, muller e. Eur J Cell Biol. 1999 Oct;78(10):749-56. doi: 10.1016/S0171-9335(99)80043-0. Eur J Cell Biol. 1999. PMID: 10569247

2

Murine liver homogentisate 1,2-dioxygenase. Purification to homogeneity and novel biochemical properties.

Schmidt SR, Müller CR, Kress W. Schmidt SR, et al. Among authors: muller cr. Eur J Biochem. 1995 Mar 1;228(2):425-30. Eur J Biochem. 1995. PMID: 7705358 Free article.

3

The use of monoclonal antibodies in diagnostic tests for Becker and Duchenne muscular dystrophy.

Gold R, Kress W, Reichmann H, Müller CR. Gold R, et al. Among authors: muller cr. J Neurol. 1993 Jan;240(1):21-4. doi: 10.1007/BF00838441. J Neurol. 1993. PMID: 8423459

4

Estimate of severe autosomal recessive limb-girdle muscular dystrophy (LGMD2C, LGMD2D) among sporadic muscular dystrophy males: a study of 415 familes.

Stec I, Kress W, Meng G, Müller B, Müller CR, Grimm T. Stec I, et al. Among authors: muller b, muller cr. J Med Genet. 1995 Dec;32(12):930-3. doi: 10.1136/jmg.32.12.930. J Med Genet. 1995. PMID: 8825917 Free PMC article.

5

Parental source effect on inherited mutations in the dystrophin gene of mice and humans.

Kress W, Grimm T, Müller CR, Keller H, Bittner R. Kress W, et al. Among authors: muller cr. Acta Genet Med Gemellol (Roma). 1996;45(1-2):251-3. doi: 10.1017/s0001566000001409. Acta Genet Med Gemellol (Roma). 1996. PMID: 8872041 No abstract available.

6

A synonymous codon change in the LMNA gene alters mRNA splicing and causes limb girdle muscular dystrophy type 1B.

Todorova A, Halliger-Keller B, Walter MC, Dabauvalle MC, Lochmüller H, Müller CR. Todorova A, et al. Among authors: muller cr. J Med Genet. 2003 Oct;40(10):e115. doi: 10.1136/jmg.40.10.e115. J Med Genet. 2003. PMID: 14569138 Free PMC article. No abstract available.

7

Risk assessment and genetic counseling in families with Duchenne muscular dystrophy.

Grimm T, Kress W, Meng G, Müller CR. Grimm T, et al. Among authors: muller cr. Acta Myol. 2012 Dec;31(3):179-83. Acta Myol. 2012. PMID: 23620649 Free PMC article.

8

A 400-kb tandem duplication within the dystrophin gene leads to severe Becker muscular dystrophy.

Gold R, Kress W, Bettecken T, Reichmann H, Müller CR. Gold R, et al. Among authors: muller cr. J Neurol. 1994 Mar;241(5):331-4. doi: 10.1007/BF00868442. J Neurol. 1994. PMID: 8006687

9

Cloning of the homogentisate 1,2-dioxygenase gene, the key enzyme of alkaptonuria in mouse.

Schmidt SR, Gehrig A, Koehler MR, Schmid M, Müller CR, Kress W. Schmidt SR, et al. Among authors: muller cr. Mamm Genome. 1997 Mar;8(3):168-71. doi: 10.1007/s003359900383. Mamm Genome. 1997. PMID: 9069115

10

Molecular defects in alkaptonuria.

Gehrig A, Schmidt SR, Müller CR, Srsen S, Srsnova K, Kress W. Gehrig A, et al. Among authors: muller cr. Cytogenet Cell Genet. 1997;76(1-2):14-6. doi: 10.1159/000134501. Cytogenet Cell Genet. 1997. PMID: 9154114

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