Hochschulschrift
Analyse von im Lynch-Syndrom identifizierten MLH1-Keimbahnmutationen auf molekulare und zelluläre Aspekte der DNA Mismatch-Reparatur
- Alternative title
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Analysis of molecular and cellular issues of Lynch Syndrome MLH1 Mutations
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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Online-Ressource
- Language
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Deutsch
- Notes
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Kiel, Christian-Albrechts-Universität, Diss., 2012
- Keyword
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Lynch-Syndrom
Mismatch
Mutation
Keimbahn
Reparatur
Colonkrebs
Tumor
Krebs
Krebs
Onkologie
- Event
-
Veröffentlichung
- (where)
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Kiel
- (who)
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Universitätsbibliothek Kiel
- (when)
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2012
- Creator
- URN
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urn:nbn:de:gbv:8-diss-83778
- Rights
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Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:52 AM CEST
Data provider
This object is provided by:
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Object type
- Hochschulschrift
Associated
- Hinrichsen, Inga Malena
- Universitätsbibliothek Kiel
Time of origin
- 2012
Other Objects (12)
Analyse von im Lynch-Syndrom identifizierten MLH1-Keimbahnmutationen auf molekulare und zelluläre Aspekte der DNA-Mismatch-Reparatur
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Funktionelle Analyse des MLH1·ITGA9-Fusionsproteins einer Lynch-Syndrom-Familie
A rare large duplication of MLH1 identified in Lynch syndrome
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Lynch syndrome-associated endometrial carcinoma with MLH1 germline mutation and MLH1 promoter hypermethylation: a case report and literature review
MLH1 Exon 12 Gene Deletion Leading to Lynch Syndrome: A Case Report
A novel MLH1 intronic variant in a young Japanese patient with Lynch syndrome
Untersuchungen zu Abbaumechanismen von Mismatch-Reparatur-Enzymen : Inhibition des MLH1-Abbaus und Stabilisierung von MLH1-Missense-Varianten im humanen Zellsystem
Constitutional mismatch repair deficiency mimicking Lynch syndrome is associated with hypomorphic mismatch repair gene variants
Frequent mismatch-repair defects link prostate cancer to Lynch syndrome
Analyse von im Lynch-Syndrom identifizierten MLH1-Keimbahnmutationen auf molekulare und zelluläre Aspekte der DNA-Mismatch-Reparatur
Screening of the DNA mismatch repair genes MLH1, MSH2 and MSH6in a Greek cohort of Lynch syndrome suspected families
Funktionelle Analyse des MLH1·ITGA9-Fusionsproteins einer Lynch-Syndrom-Familie
A rare large duplication of MLH1 identified in Lynch syndrome
A Chinese family affected by lynch syndrome caused by MLH1 mutation
Novel MLH1 nonsense variant in a patient with suspected Lynch syndrome
Lynch syndrome-associated endometrial carcinoma with MLH1 germline mutation and MLH1 promoter hypermethylation: a case report and literature review
MLH1 Exon 12 Gene Deletion Leading to Lynch Syndrome: A Case Report
A novel MLH1 intronic variant in a young Japanese patient with Lynch syndrome
Untersuchungen zu Abbaumechanismen von Mismatch-Reparatur-Enzymen : Inhibition des MLH1-Abbaus und Stabilisierung von MLH1-Missense-Varianten im humanen Zellsystem
Constitutional mismatch repair deficiency mimicking Lynch syndrome is associated with hypomorphic mismatch repair gene variants
Frequent mismatch-repair defects link prostate cancer to Lynch syndrome
Analyse von im Lynch-Syndrom identifizierten MLH1-Keimbahnmutationen auf molekulare und zelluläre Aspekte der DNA-Mismatch-Reparatur
Screening of the DNA mismatch repair genes MLH1, MSH2 and MSH6in a Greek cohort of Lynch syndrome suspected families
Funktionelle Analyse des MLH1·ITGA9-Fusionsproteins einer Lynch-Syndrom-Familie
A rare large duplication of MLH1 identified in Lynch syndrome
A Chinese family affected by lynch syndrome caused by MLH1 mutation
Novel MLH1 nonsense variant in a patient with suspected Lynch syndrome
Lynch syndrome-associated endometrial carcinoma with MLH1 germline mutation and MLH1 promoter hypermethylation: a case report and literature review
MLH1 Exon 12 Gene Deletion Leading to Lynch Syndrome: A Case Report
A novel MLH1 intronic variant in a young Japanese patient with Lynch syndrome
Untersuchungen zu Abbaumechanismen von Mismatch-Reparatur-Enzymen : Inhibition des MLH1-Abbaus und Stabilisierung von MLH1-Missense-Varianten im humanen Zellsystem
Constitutional mismatch repair deficiency mimicking Lynch syndrome is associated with hypomorphic mismatch repair gene variants