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5. Epo deficiency alters cardiac adaptation to chronic hypoxia

6. Pleiotropic and diverse expression of ZFHX1B gene transcripts during mouse and human development supports the various clinical manifestations of the “Mowat–Wilson” syndrome

7. Identification of novel genes and altered signaling pathways in the retinal pigment epithelium during the Royal College of Surgeons rat retinal degeneration

9. New Splicing-site Mutations in the SURF1Gene in Leigh Syndrome Patients

10. Homozygous Deletion in the Coding Sequence of the c-mer Gene in RCS Rats Unravels General Mechanisms of Physiological Cell Adhesion and Apoptosis

12. Mapping of a Congenital Microcoria Locus to 13q31-q32

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