Miriam Mergen
Overview
Explore the profile of Miriam Mergen including associated specialties, affiliations and a list of published articles.
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5
Citations
182
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Recent Articles
1.
Boehlke C, Janusch H, Hamann C, Powelske C, Mergen M, Herbst H, et al.
PLoS One
. 2015 Oct;
10(10):e0140378.
PMID: 26465598
Ift88 is a central component of the intraflagellar transport (Ift) complex B, essential for the building of cilia and flagella from single cell organisms to mammals. Loss of Ift88 results...
2.
Heck D, Mergen M, Ganner A, Pelisek J, Mader I, Weiller C, et al.
BMC Neurol
. 2014 Nov;
14:210.
PMID: 25369758
Background: Polyneuropathy organomegaly endocrinopathy M-protein skin changes (POEMS) syndrome is a rare cause of polyneuropathy. Calciphylaxis, a severe disease leading to necrotic ulcers of the skin, is associated with POEMS...
3.
Mergen M, Engel C, Muller B, Follo M, Schafer T, Jung M, et al.
Nephrol Dial Transplant
. 2013 Sep;
28(11):2744-53.
PMID: 24026243
Background: Nephronophthisis (NPH) is a rare recessive disease caused by several different gene mutations. Most gene products localize to the cilium, and thus, the various NPH manifestations including kidney cysts...
4.
Hoff S, Halbritter J, Epting D, Frank V, Nguyen T, van Reeuwijk J, et al.
Nat Genet
. 2013 Jun;
45(8):951-6.
PMID: 23793029
Nephronophthisis is an autosomal recessive cystic kidney disease that leads to renal failure in childhood or adolescence. Most NPHP gene products form molecular networks. Here we identify ANKS6 as a...
5.
Kenzel S, Mergen M, von Susskind-Schwendi J, Wennekamp J, Deshmukh S, Haeffner M, et al.
J Immunol
. 2012 Sep;
189(9):4582-91.
PMID: 23018458
Group B streptococci (GBS; Streptococcus agalactiae) are a major cause of invasive infections in newborn infants and in patients with type 2 diabetes. Both patient groups exhibit peripheral insulin resistance...