H K Schackert
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Explore the profile of H K Schackert including associated specialties, affiliations and a list of published articles.
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82
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Recent Articles
1.
Serra A, Gorgens H, Alhadad K, Ziegler A, Fitze G, Schackert H
Ann Hum Genet
. 2009 Feb;
73(2):147-51.
PMID: 19183406
Hirschsprung disease (HSCR) is transmitted in a complex pattern of inheritance and is mostly associated with variants in the RET proto-oncogene. However, RET mutations are only identified in 15-20% of...
2.
Noack B, Gorgens H, Hempel U, Fanghanel J, Hoffmann T, Ziegler A, et al.
J Dent Res
. 2008 Sep;
87(10):958-63.
PMID: 18809751
Cathepsin C (CTSC) mutations are known to cause Papillon-Lefèvre syndrome. The aim of this study was to examine the association of CTSC genotype with susceptibility to non-syndromic aggressive periodontitis. The...
3.
Pistorius S, Schackert H, Saeger H
Chirurg
. 2007 Apr;
78(6):561-71.
PMID: 17458520
Familial tumors of the gastrointestinal tract, which often appear as autosomal-dominantly inherited tumor syndromes, account for only a small proportion of all gastrointestinal tumors. With the opportunities of modern molecular...
4.
Schmitz M, Temme A, Senner V, Ebner R, Schwind S, Stevanovic S, et al.
Br J Cancer
. 2007 Mar;
96(8):1293-301.
PMID: 17375044
Prognosis for patients suffering from malignant glioma has not substantially improved. Specific immunotherapy as a novel treatment concept critically depends on target antigens, which are highly overexpressed in the majority...
5.
Noack B, Gorgens H, Hoffmann T, Schackert H
J Clin Periodontol
. 2006 Sep;
33(11):779-83.
PMID: 16965521
Objective: The CARD15 gene encodes a protein that acts as an intracellular receptor of bacterial products, thus playing an important role in the innate immune response. Recently, CARD15 gene variants...
6.
Kruger S, Emig M, Lohse P, Ehninger G, Hochhaus A, Schackert H
Leukemia
. 2005 Nov;
20(2):354-5.
PMID: 16307017
No abstract available.
7.
Kruger S, Bier A, Engel C, Mangold E, Pagenstecher C, Knebel Doeberitz M, et al.
J Med Genet
. 2005 Oct;
42(10):769-73.
PMID: 16199549
The polymorphic variants at codon 72 of the p53 gene were shown to be functionally distinct in vitro, whereby the arginine (arg) variant induces apoptosis more efficiently than the proline...
8.
Temme A, Herzig E, Weigle B, Morgenroth A, Schmitz M, Kiessling A, et al.
Hum Gene Ther
. 2005 Mar;
16(2):209-22.
PMID: 15761261
Glioblastoma multiforme (GBM) is a highly malignant brain tumor that is resistant to conventional radiotherapy and chemotherapy. The median survival time of patients with GBM has remained less than 2...
9.
Martinez R, Schackert H, Appelt H, Plaschke J, Baretton G, Schackert G
J Cancer Res Clin Oncol
. 2005 Jan;
131(2):87-93.
PMID: 15672285
Purpose: Genetic instability is a hallmark of glioblastoma multiforme (GBM). Microsatellite instability (MSI) is a significant event in the tumorigenesis of many sporadic malignancies. The aim of our investigation was...
10.
Fitze G, Saeger H, Roesner D, Schackert H
Klin Padiatr
. 2004 Sep;
216(5):270-6.
PMID: 15455293
Introduction: Heredity of MEN2 syndromes is caused by a heterozygous germline mutation in the RET proto-oncogene. This study describes families with rare noncysteine codon 790/791 mutations and discusses the genotype-phenotype...