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Mitochondrion|June 10, 2014
Heterologous expression from the human D-Loop in organelloC B Jackson, C Zbinden, S Gallati, et al.
Respiration; International Review of Thoracic Diseases|November 9, 2000
Early detection of lung disease and its association with the nutritional status, genetic background and life events in patients with cystic fibrosisR Kraemer, C Aebi, C Casaulta Aebischer, et al.
Molecular Microbiology|June 13, 2001
Overlapping sense and antisense transcription units in Trypanosoma bruceiM Liniger, K Bodenmüller, E Pays, et al.
The European Respiratory Journal|August 9, 2001
High morbidity and mortality in cystic fibrosis patients compound heterozygous for 3905insT and deltaF508A Schibler, I Bolt, S Gallati, et al.
Klinische Padiatrie|September 17, 2005
[Menkes' disease: heterozygosity testing by quantitative real-time PCR and the dilemma of therapeutic support]O Rittinger, G Sander, A Schaller, et al.
European Neurology|May 9, 2003
Clinical and molecular analysis of chinese patients with thyrotoxic periodic paralysisL Chen, D Lang, X W Ran, et al.
The Journal of Clinical Endocrinology and Metabolism|September 11, 2001
New autosomal recessive mutation of the TSH-beta subunit gene causing central isolated hypothyroidismJ M Vuissoz, J Deladoëy, A Buyukgebiz, et al.
Mitochondrion|February 5, 2011
Impairment of mitochondrial tRNAIle processing by a novel mutation associated with chronic progressive external ophthalmoplegiaA Schaller, R Desetty, D Hahn, et al.
Molecular and Biochemical Parasitology|September 12, 2001
Genetic variants of the TbAT1 adenosine transporter from African trypanosomes in relapse infections following melarsoprol therapyE Matovu, F Geiser, V Schneider, et al.
Eye (London, England)|February 17, 2007
Glaucoma phenotype in a large Swiss pedigree with the myocilin Gly367Arg mutationM E Iliev, S Bodmer, S Gallati, et al.
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