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MEN1 gene mutation analysis of sporadic adrenocortical lesions
Birgit Görtz
, Jürgen Roth
, Ernst J.M. Speel
, Akiko Krähenmann
,
Ronald R. De Krijger
, Xavier Matias-Guiu
, Seraina Muletta-Feurer
, Katrin Rütmann
, Parvin Saremaslani
, Philipp U. Heitz
, Paul Komminoth
Onderzoeksoutput
:
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Artikel
›
peer review
96
Citaten (Scopus)
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Keyphrases
Adenoma
20%
Adrenal Cortex
20%
Adrenal Tumor
20%
Adrenocortical
100%
Adrenocortical Adenoma
20%
Adrenocortical Carcinoma
20%
Atypical Carcinoid
20%
Benign Lesion
20%
Carcinoma
20%
Clinical Signs
20%
Complete Coding Sequence
20%
Cosmid
20%
Exon 2
20%
Family History
20%
Fluorescence in Situ Hybridization
40%
Fluorescence in Situ Hybridization Analysis
20%
Gel Electrophoresis
20%
Germline mutation
20%
Heteroduplex
20%
Hyperplasia
20%
Hyperplastic Lesions
20%
Inactivating mutation
20%
Loss of Heterozygosity
80%
Lung
20%
MEN1 Gene
100%
Microsatellite Markers
20%
Molecular Study
20%
Mutation Analysis
20%
Neoplastic Lesions
20%
Neuroendocrine Carcinoma
20%
Newly Reported
20%
Non-radioactive
20%
PCR-based
20%
Polymorphism
20%
Single-strand Conformation Polymorphism Analysis
20%
Somatic mutation Analysis
100%
Splicing mutation
40%
Stop Codon mutation
20%
Tumor
100%
Tumor Samples
20%
Tumor Suppressor Gene
20%
Tumorigenesis
20%
Medicine and Dentistry
Adenoma
16%
Adrenal Adenoma
16%
Adrenal Cortex
16%
Adrenal Cortex Carcinoma
16%
Adrenal Cortex Tumor
16%
Carcinogenesis
16%
Carcinoid
16%
Carcinoma
16%
Cosmid
16%
Exon
16%
Family History
16%
Fluorescence in Situ Hybridization
50%
Gel Electrophoresis
16%
Gene Mutation
100%
Germline Mutation
16%
Heteroduplex
16%
Heterozygosity
66%
Hyperplasia
16%
Intron
33%
Lung
16%
Microsatellite Marker
16%
Neoplasm
100%
Neuroendocrine Carcinoma
16%
Single Strand Conformation Polymorphism
16%
Somatics
16%
Stop Codon
16%
Tumor Suppressor Gene
16%
Neuroscience
Adrenal Cortex
33%
Carcinogenesis
33%
Carcinoid
33%
Cosmid
33%
Exon
33%
Gel Electrophoresis
33%
Gene Mutation
100%
Germ Cell
33%
Heteroduplex
33%
Hyperplasia
33%
In Situ Hybridization
100%
Intron
66%
Microsatellite
33%
Somatics
33%
Stop Codon
33%
Tumor Suppressor Gene
33%
Biochemistry, Genetics and Molecular Biology
Carcinogenesis
11%
Cosmid
11%
Exon
11%
Fluorescence in Situ Hybridization
33%
Gel Electrophoresis
11%
Gene Mutation
100%
Germline Mutation
11%
Heteroduplex
11%
Intron
22%
Loss of Heterozygosity
44%
MEN1
100%
Microsatellite Marker
11%
Single-Strand Conformation Polymorphism
11%
Stop Codon
11%
Tumor Suppressor Gene
11%