A. Hafner

发表

A mutation in Tubb2b, a human polymicrogyria gene, leads to lethality and abnormal cortical development in the mouse.

Amy Bernard, D. Beier, M. Donlin, 2013, Human molecular genetics.

Regulation of the mPTP by SIRT3-mediated deacetylation of CypD at lysine 166 suppresses age-related cardiac hypertrophy

D. Sinclair, A. Rosenzweig, C. Palmeira, 2010, Aging.

I-cell disease-like phenotype in mice deficient in mannose 6-phosphate receptors

K. Figura, W. Schmahl, P. Schmidt, 1998, Transgenic Research.

Alternative mechanisms for trafficking of lysosomal enzymes in mannose 6-phosphate receptor-deficient mice are cell type-specific.

K. von Figura, K. Figura, W. Schmahl, 1999, Journal of cell science.

Reconstitution of gene expression from a regulatory‐protein‐deficient hepatitis B virus genome by cell‐permeable HBx protein

E. Hildt, Boerries Brandenburg, A. Hafner, 2003, EMBO reports.

ProNGF, Sortilin, and Age‐related Neurodegeneration

T. Cowen, C. Thrasivoulou, R. Al-Shawi, 2007, Annals of the New York Academy of Sciences.

Cathepsin L deficiency as molecular defect of furless: hyperproliferation of keratinocytes and pertubation of hair follicle cycling

J. Deussing, C. Peters, K. von Figura, 2000, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

SIRT1 Redistribution on Chromatin Promotes Genomic Stability but Alters Gene Expression during Aging

F. Alt, T. Prolla, P. Loerch, 2008, Cell.

SIRT1 is required for AMPK activation and the beneficial effects of resveratrol on mitochondrial function.

R. de Cabo, D. Sinclair, R. Coppari, 2012, Cell metabolism.

SIRT2 induces the checkpoint kinase BubR1 to increase lifespan

D. Sinclair, D. Baker, Shaday Michán, 2014, The EMBO journal.

Prolyl Isomerase Pin1 Regulates Neuronal Differentiation via β-Catenin

Akihide Ryo, D. Sinclair, A. Ryo, 2012, Molecular and Cellular Biology.

Neurotoxic and neurotrophic roles of proNGF and the receptor sortilin in the adult and ageing nervous system

Christopher Thrasivoulou, Simon Lovestone, S. Lovestone, 2008, The European journal of neuroscience.

Targeted disruption of the arylsulfatase B gene results in mice resembling the phenotype of mucopolysaccharidosis VI.

C. Peters, K. von Figura, P. Saftig, 1996, Proceedings of the National Academy of Sciences of the United States of America.

SIRT 2 induces the checkpoint kinase BubR 1 to increase lifespan

Anthony, D. Sinclair, M. Rosenzweig, 2014 .

Prolyl Isomerase Pin1 Regulates Neuronal Differentiation via β-Catenin

D. Sinclair, A. Ryo, K. Lu, 2012, Molecular and Cellular Biology.

A mutation in Tubb2b, a human polymicrogyria gene, leads to lethality and abnormal cortical development in the mouse.

Amy Bernard, D. Beier, M. Donlin, 2013, Human molecular genetics.