B. Korge

发表

A leucine→proline mutation in the H1 subdomain of keratin 1 causes epidermolytic hyperkeratosis

S. Bale, P. Steinert, J. DiGiovanna, 1992, Cell.

Genetic analysis of a severe case of Netherton syndrome and application for prenatal testing

I. Hausser, B. Korge, R. Maiwald, 2002, The British journal of dermatology.

Altered proliferation, synthetic activity, and differentiation of cultured human sebocytes in the absence of vitamin A and their modulation by synthetic retinoids.

C. Zouboulis, D. Mischke, C. Orfanos, 1993, The Journal of investigative dermatology.

Effects of 13-cis-retinoic acid, all-trans-retinoic acid, and acitretin on the proliferation, lipid synthesis and keratin expression of cultured human sebocytes in vitro.

H. Gollnick, C. Zouboulis, C. Orfanos, 1991, The Journal of investigative dermatology.

Physical mapping of a functional cluster of epidermal differentiation genes on chromosome 1q21.

P. Steinert, D. Mischke, A. Ziegler, 1993, Genomics.

Real‐world effectiveness of guselkumab in patients with psoriasis: Health‐related quality of life and efficacy data from the noninterventional, prospective, German multicenter PERSIST trial

M. Sticherling, S. Gerdes, F. Wiemers, 2021, The Journal of dermatology.

Polymorphic Keratins as Detected by PCR and SSCP

D. Mischke, R. Wanner, B. Korge, 1994 .

Recessive epidermolytic hyperkeratosis caused by a previously unreported termination codon mutation in the keratin 10 gene.

P. Terheyden, T. Krieg, C. Rose, 2009, The Journal of investigative dermatology.

A premature stop codon mutation in the 2B helix termination peptide of keratin 5 in a German epidermolysis bullosa simplex Dowling-Meara case.

W. Küster, B. Korge, F. B. Müller, 1999, The Journal of investigative dermatology.

Novel K5 and K14 mutations in German patients with the Weber-Cockayne variant of epidermolysis bullosa simplex.

L. Bruckner-Tuderman, W. Küster, B. Korge, 1998, The Journal of investigative dermatology.

A mutational hotspot in the 2B domain of human hair basic keratin 6 (hHb6) in monilethrix patients.

A. Messenger, E. Healy, J. Rees, 1998, The Journal of investigative dermatology.

Fine mapping of the Darier's disease locus on chromosome 12q.

S. Bale, G. Richard, O. Mcbride, 1994, The Journal of investigative dermatology.

Identification of novel mutations in basic hair keratins hHb1 and hHb6 in monilethrix: implications for protein structure and clinical phenotype.

D. Parry, A. Messenger, E. Healy, 1999, The Journal of investigative dermatology.

Genetic analysis of the epidermal differentiation complex (EDC) on human chromosome 1q21: chromosomal orientation, new markers, and a 6-Mb YAC contig.

I. Marenholz, I. Ragoussis, D. Mischke, 1996, Genomics.

A cDNA encoding the human type I hair keratin hHal.

H. Winter, B. Korge, J. Schweizer, 1995, Biochimica et biophysica acta.

Hailey-Hailey disease maps to a 5 cM interval on chromosome 3q21-q24.

S. Bale, G. Richard, M. Annicchiarico-Petruzzelli, 1995, The Journal of investigative dermatology.

Human Scalp Dermal Papilla and Fibrous Sheath Cells have a different expression profile of Matrix Metalloproteinases in vitro when compared to Scalp Dermal Fibroblasts

T. Krieg, P. Zigrino, C. Mauch, 2005, Archives of Dermatological Research.

Adrenomedullin: expression and possible role in human skin and hair growth

M. Philpott, S. Müller-Röver, S. Kapas, 2003, The British journal of dermatology.

Darier disease – novel mutations in ATP2A2 and genotype–phenotype correlation

S. Bale, J. Uitto, G. Richard, 2001, Experimental dermatology.

Normal psoriatic epidermis expression of hyperproliferation-associated keratins

D. Mischke, R. Stadler, M. Thewes, 2004, Archives of Dermatological Research.

Influence of Retinoids on the Keratin Profile in Normal and Spontaneously Transformed Human Keratinocytes

D. Mischke, R. Stadler, B. Korge, 1993 .

Quality-of-Life Outcomes, Effectiveness and Tolerability of Apremilast in Patients with Plaque Psoriasis and Routine German Dermatology Care: Results from LAPIS-PSO

J. Roemmler-Zehrer, K. Reich, N. Magnolo, 2021, Dermatology and Therapy.

Keratin and keratinization.

W. James, B. Korge, D. P. Smack, 1994, Journal of the American Academy of Dermatology.

A missense mutation in connexin26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel's syndrome) in three unrelated families.

E. Maestrini, A. Monaco, E. Calzolari, 1999, Human molecular genetics.

Solid basal cell epithelioma (BCE) possibly originates from the outer root sheath of the hair follicle.

I. Kurokawa, C. Orfanos, M. Asada, 1993, Acta dermato-venereologica.

Effect of retinoids on hyperproliferation-associated keratins K6 and K16 in cultured human keratinocytes: a quantitative analysis.

D. Mischke, R. Stadler, B. Korge, 1990, The Journal of investigative dermatology.

Loricrin mutation in Vohwinkel's keratoderma is unique to the variant with ichthyosis.

H. Iizuka, C. Munro, R. Eady, 1997, The Journal of investigative dermatology.

A human keratin 10 knockout causes recessive epidermolytic hyperkeratosis.

Marcel Huber, D. Hohl, M. Huber, 2006, Human molecular genetics.

Extensive size polymorphism of the human keratin 10 chain resides in the C-terminal V2 subdomain due to variable numbers and sizes of glycine loops.

O. Mcbride, P. Steinert, D. Mischke, 1992, Proceedings of the National Academy of Sciences of the United States of America.

Desmosome assembly and keratin network formation after Ca2+/serum induction and UVB radiation in Hailey-Hailey keratinocytes.

B. Korge, M. Bernards, 2000, The Journal of investigative dermatology.

Genes encoding structural proteins of epidermal cornification and S100 calcium-binding proteins form a gene complex ("epidermal differentiation complex") on human chromosome 1q21.

I. Marenholz, D. Mischke, A. Ziegler, 1996, The Journal of investigative dermatology.

The two size alleles of human keratin 1 are due to a deletion in the glycine-rich carboxyl-terminal V2 subdomain.

P. Steinert, D. Mischke, J. Compton, 1992, The Journal of investigative dermatology.

The Cornified Cell Envelope: Loricrin and Transglutaminases

K. Yoneda, O. Mcbride, P. Steinert, 1992, The Journal of dermatology.

Successful treatment of Hailey-Hailey disease with a scanned carbon dioxide laser.

K. Scharffetter-Kochanek, N. Hunzelmann, J. Lasch, 2000, Acta dermato-venereologica.

First "Real-World" Insights on Apremilast Treatment for Patients with Plaque Psoriasis from the LAPIS-PSO Study: An Interim Analysis

K. Reich, B. Korge, Stefanie Bomas, 2017 .

Cultivation of Human Sebocytes in vitro: Cell Characterization and Influence of Synthetic Retinoids

H. Gollnick, C. Zouboulis, C. Orfanos, 1991 .

Glycine loops in proteins: their occurrence in certain intermediate filament chains, loricrins and single-stranded RNA binding proteins.

A. Steven, P. Steinert, S. Haynes, 1991, International journal of biological macromolecules.

Real‐world evidence from the non‐interventional, prospective, German multicentre PERSIST study of patients with psoriasis after 1 year of treatment with guselkumab

K. Asadullah, M. Sticherling, S. Gerdes, 2022, Journal of the European Academy of Dermatology and Venereology : JEADV.

[Cutaneous metastases from a leiomyosarcoma of the testicular tunica albuginea].

T. Krieg, K. Scharffetter-Kochanek, N. Hunzelmann, 2000, Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete.

Novel and recurrent mutations in keratin KRT5 and KRT14 genes in epidermolysis bullosa simplex: implications for disease phenotype and keratin filament assembly

T. Krieg, L. Bruckner-Tuderman, W. Küster, 2006, Human mutation.

Flecked chorioretinopathy associated with Birt-Hogg-Dubé syndrome

P. Walter, B. Kirchhof, K. Heimann, 1997, Graefe's Archive for Clinical and Experimental Ophthalmology.

Real‐world effectiveness and safety of tildrakizumab in long‐term treatment of plaque psoriasis: Results from the non‐interventional, prospective, multicentre study TILOT

A. Tsianakas, U. Schwichtenberg, B. Korge, 2022, Journal of the European Academy of Dermatology and Venereology : JEADV.

Linkage of epidermolytic hyperkeratosis to the type II keratin gene cluster on chromosome 12q

C. Amos, S. Bale, O. Mcbride, 1992, Nature Genetics.

Effectiveness, safety and quality-of-life effects of guselkumab and ustekinumab in patients with psoriasis: Week 104 results from the non-interventional, prospective, German multicentre PERSIST study.

K. Asadullah, M. Sticherling, F. Kreimendahl, 2023, Journal of the European Academy of Dermatology and Venereology : JEADV.

Sequence data and chromosomal localization of human type I and type II hair keratin genes.

P. Lichter, H. Winter, T. Krieg, 1995, Experimental cell research.

Pityriasis Rosea

B. Korge, 1908, Der Hautarzt.