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9 (5), pp. 437 - 48 (1999)
Genomic structure and comparative analysis of nine Fugu genes: conservation of synteny with human chromosome Xp22.2-p22.1. Genome Res 3022.
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Identification and characterization of G90, a novel mouse RNA that lacks an extensive open reading frame. Gene 3023.
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Regulation and expression of the murine PMP22 gene. Mamm Genome 3024.
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80 (1-4), pp. 165 - 72 (1998)
Beta-heterochromatin in mammals: evidence from studies in Microtus agrestis based on the extensive accumulation of L1 and non-L1 retroposons in the heterochromatin. Cytogenet Cell Genet 3025.
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6 (2), pp. 114 - 20 (1998)
Evidence against a major role of PEG1/MEST in Silver-Russell syndrome. Eur J Hum Genet 3026.
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245 (1), pp. 272 - 7 (1998)
Absence of an obvious molecular imprinting mechanism in a human fetus with monoallelic IGF2R expression. Biochem Biophys Res Commun 3027.
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42 (2), pp. 236 - 44 (1997)
Monoallelic expression of human PEG1/MEST is paralleled by parent-specific methylation in fetuses. Genomics 3028.
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73 (3), pp. 171 - 8 (1996)
Evolution of the gonosomal heterochromatin of Microtus agrestis: rapid amplification of a large, multimeric, repeat unit containing a 3.0-kb (GATA)11-positive, middle repetitive element. Cytogenet Cell Genet 3029.
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35 (2), pp. 380 - 2 (1996)
The MAS proto-oncogene is not imprinted in humans. Genomics 3030.
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31 (2), pp. 158 - 66 (1996)
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The SYSTERS Protein Family Database in 2005.
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3035.
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Blocking TLR2 in vivo protects against accumulation of inflammatory cells and neuronal injury in experimental stroke.
Book (9)
3039.
Book
Limb Malformations – An Atlas of Genetic Disorders of Limb Development. Springer-Verlag, Berlin, Heidelberg (2014), 767 pp.
3040.
Book
Medical Advancements in Aging and Regenerative Technologies: Clinical Tools and Applications. IGI Global (2012)