Zenker, Martin 1964-
Zenker, Martin
Zenker, Martin, 19..-....
Martin Zenker researcher (ORCID 0000-0003-1618-9269)
VIAF ID: 316011396 (Personal)
Permalink: http://viaf.org/viaf/316011396
Preferred Forms
- 100 0 _ ‡a Martin Zenker ‡c researcher (ORCID 0000-0003-1618-9269)
- 200 _ | ‡a Zenker ‡b Martin
- 100 1 _ ‡a Zenker, Martin
-
- 100 1 _ ‡a Zenker, Martin
- 100 1 _ ‡a Zenker, Martin ‡d 1964-
- 100 1 _ ‡a Zenker, Martin, ‡d 19..-....
4xx's: Alternate Name Forms (3)
5xx's: Related Names (2)
- 551 _ _ ‡a Erlangen ‡4 ortg ‡4 https://d-nb.info/standards/elementset/gnd#placeOfBirth
- 510 2 _ ‡a Otto-von-Guericke-Universität Magdeburg ‡b Medizinische Fakultät ‡4 affi ‡4 https://d-nb.info/standards/elementset/gnd#affiliation ‡e Affiliation
Works
Title | Sources |
---|---|
Aberrant neuronal activity-induced signaling and gene expression in a mouse model of RASopathy | |
Albuminuria jako cecha fenotypowa heterozygot, nosicieli mutacji genu beta-2 laminy | |
Behavioral phenotype in five individuals with de novo mutations within the GRIN2B gene | |
A Case Report: First Long-Term Treatment With Burosumab in a Patient With Cutaneous-Skeletal Hypophosphatemia Syndrome | |
Characteristic dental pattern with hypodontia and short roots in Fraser syndrome | |
Clinical and Genetic Evaluation of Patients with KATP Channel Mutations from the German Registry for Congenital Hyperinsulinism | |
clinical significance of A2ML1 variants in Noonan syndrome has to be reconsidered | |
Estimated prevalence of harmful alcohol consumption in pregnant and nonpregnant women in Saxony-Anhalt (NorthEast Germany) using biomarkers | |
Expanding the genotypic and phenotypic spectrum of severe serine biosynthesis disorders | |
Extracranial vascular anomalies driven by RAS/MAPK variants: spectrum and genotype–phenotype correlations | |
Functional characterization of a novel TP53RK mutation identified in a family with Galloway–Mowat syndrome | |
Genetic testing in inherited endocrine disorders: joint position paper of the European reference network on rare endocrine conditions (Endo-ERN) | |
Genetic variation of the RASGRF1 regulatory region affects human hippocampus-dependent memory | |
Homozygosity mapping in children with primary nephrotic syndrome | |
Homozygotiekartierung bei Kindern mit primärem nephrotischen Syndrom | |
Human pluripotent stem cell-derived acinar/ductal organoids generate human pancreas upon orthotopic transplantation and allow disease modelling | |
Increased osteoclastogenesis contributes to bone loss in the Costello syndrome Hras G12V mouse model | |
Integration of genomic analysis and transcript expression of ABCC8 and KCNJ11 in focal form of congenital hyperinsulinism | |
Lovastatin improves impaired synaptic plasticity and phasic alertness in patients with neurofibromatosis type 1 | |
Noonan syndrome and related disorders a matter of deregulated ras signaling | |
Perkutane Elektrostimulation mit bidirektionalen Strömen am denervierten Kaninchenmuskel | |
A postzygotic SMO mutation caused the original case of Happle–Tinschert syndrome | |
QRICH1 variants in Ververi‐Brady syndrome—delineation of the genotypic and phenotypic spectrum | |
Quantifying osteosynthesis plate prominence – mathematical definitions and case study on a clavicle plate | |
Syndromic scalp defects genotype-phenotype studies in Johanson-Blizzard syndrome and Adams-Oliver syndrome | |
T cell-specific constitutive active SHP2 enhances T cell memory formation and reduces T cell activation | |
Three-dimensional morphometric analysis of the lateral clavicle and acromion: Implications for surgical treatment using subacromial support | |
Ubiquitin Ligases of the N-End Rule Pathway: Assessment of Mutations in UBR1 That Cause the Johanson-Blizzard Syndrome | |
Unusual phenotypes in patients with a pathogenic germline variant in DICER1 |