Cigarette Smoking as a Triggering Factor of Hidradenitis suppurativa

Arne König, Corinne Lehmann, Rainer Rompel, +1

Dermatology

Deficiency of PORCN, a regulator of Wnt signaling, is associated with focal dermal hypoplasia

Karl‐Heinz Grzeschik, Dorothea Bornholdt, Frank Oeffner, +14

Nature Genetics

Developmental BiologySignal TransductionTissue DevelopmentSignaling PathwayPhysiology +7

WNT5A--target of CUTL1 and potent modulator of tumor cell migration and invasion in pancreatic cancer

S Ripka, Arne König, Malte Buchholz, +6

Carcinogenesis

Tumor Growth Factor-betaCancer BiologyTumor BiologyTumor InvasionSignaling Pathway +14

IFAP Syndrome Is Caused by Deficiency in MBTPS2, an Intramembrane Zinc Metalloprotease Essential for Cholesterol Homeostasis and ER Stress Response

Frank Oeffner, Gayle Fischer, Rudolf Happle, +11

The American Journal of Human Genetics

InflammationProtein Quality ControlOxysterolAllergyBiochemistry +12

Prostacyclin-induced vasodilation in rabbit heart is mediated by ATP-sensitive potassium channels

William F. Jackson, Arne König, Thomas Dambacher, +1

American Journal of Physiology-Heart and Circulatory Physiology

Cardiovascular PharmacologyPharmacotherapyCardiovascular FunctionRabbit HeartAtp-sensitive Potassium Channels +14

Allelic loss underlies type 2 segmental Hailey-Hailey disease, providing molecular confirmation of a novel genetic concept

Pamela Poblete‐Gutiérrez, T. Wiederholt, Arne König, +6

Journal of Clinical Investigation

CytogeneticsGeneticsGenetic EpidemiologyPathologyHailey-hailey Disease +18

HID and KID syndromes are associated with the same connexin 26 mutation

Michel van Geel, Maurice A. M. Van Steensel, Wolfgang Küster, +4

British Journal of Dermatology

Prostacyclin and Nitric Oxide Contribute to the Vasodilator Action of Acetylcholine and Bradykinin in the Intact Rabbit Coronary Bed

Daniel Lamontagne, Arne König, E. Bassenge, +1

Journal of Cardiovascular Pharmacology

<i>PORCN</i>mutations in focal dermal hypoplasia: coping with lethality

Dorothea Bornholdt, Frank Oeffner, Arne König, +31

Human Mutation

Developmental BiologySomatic VariantMendelian DisorderGenetic DisorderMedicine +12

A novel missense mutation of NSDHL in an unusual case of CHILD syndrome showing bilateral, almost symmetric involvement

Arne König, Rudolf Happle, Regina Fink‐Puches, +4

Journal of the American Academy of Dermatology

Unusual CaseDevelopmental AnomalyRare DiseasesMendelian DisorderGenetic Disorder +8