Journal Article (167)
121.
Journal Article
7 (4), pp. 612 - 622 (2006)
Nonribosomal peptide synthesis in S. pombe and the architecture of ferrichrome-type siderophore synthetases in fungi. ChemBioChem: A European Journal of Chemical Biology 122.
Journal Article
126 (5), pp. 1003 - 1005 (2006)
A novel MGST2 non-synonymous mutation in a Chinese pedigree with psoriasis vulgaris. The Journal of Investigative Dermatology: Official Journal of the Society for Investigative Dermatology and the European Society for Dermatological Research 123.
Journal Article
14 (4), pp. 418 - 425 (2006)
Exonic microdeletions in the X-linked PQBP1 gene in mentally retarded patients: a pathogenic mutation and in-frame deletions of uncertain effect. European Journal of Human Genetics: the Official Journal of the European Society of Human Genetics 124.
Journal Article
34 (4), pp. 1182 - 1188 (2006)
Accuracy of DNA methylation pattern preservation by the Dnmt1 methyltransferase. Nucleic Acids Research. 125.
Journal Article
34 (3), p. e25 - e25 (2006)
High-throughput trapping of secretory pathway genes in mouse embryonic stem cells. Nucleic Acids Research (London) 126.
Journal Article
38 (3), pp. 331 - 336 (2006)
Germline KRAS mutations cause Noonan syndrome. Nature Genetics 127.
Journal Article
140 (5), pp. 427 - 33 (2006)
Delineation of a 2.2 Mb microdeletion at 5q35 associated with microcephaly and congenital heart disease. American Journal of Medical Genetics Part A 128.
Journal Article
140 (5), pp. 496 - 502 (2006)
Molecular cytogenetic analysis of a de novo interstitial deletion 5q23.3q31.2 and its phenotypic consequences. American Journal of Medical Genetics 129.
Journal Article
40 (2), pp. 234 - 246 (2006)
A fibrillin-1-fragment containing the elastin-binding-protein GxxPG consensus sequence upregulates matrix metalloproteinase-1: biochemical and computational analysis. Journal of Molecular and Cellular Cardiology (London) 130.
Journal Article
43 (2), pp. 111 - 118 (2006)
Breakpoints around the HOXD cluster result in various limb malformations. Journal of Medical Genetics 131.
Journal Article
43 (2), pp. 111 - 118 (2006)
Breakpoints around the HOXD cluster result in various limb malformations. Journal of Medical Genetics 132.
Journal Article
118 (6), pp. 708 - 715 (2006)
SNP array-based homozygosity mapping reveals MCPH1 deletion in family with autosomal recessive mental retardation and mild microcephaly. Human Genetics 133.
Journal Article
10 (1), pp. 4 - 10 (2006)
Recent advances of protein microarrays. Current Opinion in Chemical Biology 134.
Journal Article
62 (2), pp. 168 - 175 (2006)
A novel method distinguishes between mutation rates and fixation biases in patterns of single-nucleotide substitution. Journal of Molecular Evolution: the Journal of the International Society of Molecular Evolution 135.
Journal Article
78 (2), pp. 265 - 278 (2006)
ZNF674: a new KRAB-containing zinc finger gene involved in non-syndromic X-linked mental retardation. American Journal of Human Genetics: : AJHG / American Society of Human Genetics 136.
Journal Article
20 (2), pp. 362 - 363 (2006)
Platelet transfusion can mimic somatic mtDNA mutations. Leukemia: the Journal of Normal and Malignant Hemopoiese ; Official Journal of the Leukemia Research Fund U.K. 137.
Journal Article
45 (8), pp. 2504 - 2514 (2006)
EF-G-dependent GTPase on the ribosome: Conformational change and fusidic acid inhibition. Biochemistry 138.
Journal Article
69 (2), pp. 189 - 193 (2006)
Molecular characterization of a balanced chromosome translocation in psoriasis vulgaris. Clinical Genetics 139.
Journal Article
36 (2), pp. 145 - 156 (2006)
Non-parametric classification of protein secondary structures. Computers in Biology and Medicine (Elmsford, NY) 140.
Journal Article
94 (2), pp. 268 - 274 (2006)
Mitochondrial DNA mutations in renal cell carcinomas revealed no general impact on energy metabolism. British Journal of Cancer