I. Anton‐Lamprecht

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

Wera Roth, Jan M. Deussing, Vladimir A. Botchkarev et al. · The FASEB Journal · 2000 · 309 citations

Ultrastructural connective tissue abnormalities in patients with spontaneous cervicocerebral artery dissections

Tobias Brandt, E. Orberk, Armin Grau et al. · Annals of Neurology · 1998 · 239 citations

Gross Anatomy, Proven Nontraumatic Dissections, Minimally Invasive Procedure +15

A human keratin 14 "knockout": the absence of K14 leads to severe epidermolysis bullosa simplex and a function for an intermediate filament protein.

Yee-Ming Chan, I. Anton‐Lamprecht, Q C Yu et al. · Genes & Development · 1994 · 200 citations · Full text

Intermediate Filament Protein, Pathology, Keratin Network Perturbations +16

The genetic basis of epidermolysis bullosa simplex with mottled pigmentation.

J. Uttam, Elizabeth R. Hutton, Pierre A. Coulombe et al. · Proceedings of the National Academy of Sciences · 1996 · 179 citations · Full text

Medicine, Genetics, Cutaneous Biology +10

Mutations in the COL5A1 gene are causal in the Ehlers-Danlos syndromes I and II.

Anne De Paepe, Lieve Nuytinck, I. Anton‐Lamprecht et al. · PubMed · 1997 · 166 citations