Kathlen Franke
Overview
Explore the profile of Kathlen Franke including associated specialties, affiliations and a list of published articles.
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Articles
3
Citations
30
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0
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Recent Articles
1.
Hackmann K, Stadler A, Schallner J, Franke K, Gerlach E, Schrock E, et al.
Am J Med Genet A
. 2013 Sep;
161A(12):3144-9.
PMID: 24039006
We report on a de novo 0.5 Mb triplication (partial tetrasomy) of chromosome 17q25.3 in a 10-year-old girl with severe intellectual disability, infantile seizures (West syndrome), moderate hearing loss, Dandy-Walker...
2.
Rivera-Brugues N, Albrecht B, Wieczorek D, Schmidt H, Keller T, Gohring I, et al.
J Med Genet
. 2010 Oct;
48(2):136-40.
PMID: 20921020
Background: Cohen syndrome is a rare autosomal recessive disorder with a complex phenotype including psychomotor retardation, microcephaly, obesity with slender extremities, joint laxity, progressive chorioretinal dystrophy/myopia, intermittent isolated neutropenia, a...
3.
Anders A, Lilie H, Franke K, Kapp L, Stelling J, Gilles E, et al.
J Biol Chem
. 2006 Jul;
281(39):29337-48.
PMID: 16867978
The Gal4 protein represents a universally functional transcription activator, which in yeast is regulated by protein-protein interaction of its transcription activation domain with the inhibitor Gal80. Gal80 inhibition is relieved...