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Hereditary Cancer in Clinical Practice
|
January 26, 2019
Diagnostic yield and clinical utility of a comprehensive gene panel for hereditary tumor syndromes
Jonas Henn, Isabel Spier, Ronja S Adam, et al.
The Journal of Biological Chemistry
|
October 6, 2009
Inhibition of the equilibrative nucleoside transporter 1 and activation of A2A adenosine receptors by 8-(4-chlorophenylthio)-modified cAMP analogs and their hydrolytic products
Oliver Waidmann, Thomas Pleli, Karel Dvorak, et al.
European Journal of Pediatrics
|
March 28, 2007
Hypothesis: Possible role of retinoic acid therapy in patients with biallelic mismatch repair gene defects
Sven Gottschling, Harald Reinhard, Constanze Pagenstecher, et al.
Molecular Cancer
|
January 25, 2014
Reduced migration of MLH1 deficient colon cancer cells depends on SPTAN1
Inga Hinrichsen, Benjamin Philipp Ernst, Franziska Nuber, et al.
Molecular Carcinogenesis
|
August 24, 2018
DNA mismatch repair activity of MutLα is regulated by CK2-dependent phosphorylation of MLH1 (S477)
Isabel M Weßbecher, Inga Hinrichsen, Sebastian Funke, et al.
Nucleic Acids Research
|
December 1, 2006
Mutations in the MutSalpha interaction interface of MLH1 can abolish DNA mismatch repair
Guido Plotz, Christoph Welsch, Luis Giron-Monzon, et al.
Nucleic Acids Research
|
May 24, 2023
A conserved motif in the disordered linker of human MLH1 is vital for DNA mismatch repair and its function is diminished by a cancer family mutation
Karla Wolf, Jan Kosinski, Toby J Gibson, et al.
Plos One
|
March 12, 2019
Downregulation of SPTAN1 is related to MLH1 deficiency and metastasis in colorectal cancer
Anne Ackermann, Christopher Schrecker, Dimitra Bon, et al.
Carcinogenesis
|
December 6, 2014
Functional testing strategy for coding genetic variants of unclear significance in MLH1 in Lynch syndrome diagnosis
Inga Hinrichsen, Dieter Schäfer, Deborah Langer, et al.
Human Mutation
|
June 28, 2012
Comprehensive functional assessment of MLH1 variants of unknown significance
Ester Borràs, Marta Pineda, Angela Brieger, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 49) with videos related to
Sort By:
Page
of 5
Hereditary Cancer in Clinical Practice
|
January 26, 2019
Diagnostic yield and clinical utility of a comprehensive gene panel for hereditary tumor syndromes
Jonas Henn, Isabel Spier, Ronja S Adam, et al.
The Journal of Biological Chemistry
|
October 6, 2009
Inhibition of the equilibrative nucleoside transporter 1 and activation of A2A adenosine receptors by 8-(4-chlorophenylthio)-modified cAMP analogs and their hydrolytic products
Oliver Waidmann, Thomas Pleli, Karel Dvorak, et al.
European Journal of Pediatrics
|
March 28, 2007
Hypothesis: Possible role of retinoic acid therapy in patients with biallelic mismatch repair gene defects
Sven Gottschling, Harald Reinhard, Constanze Pagenstecher, et al.
Molecular Cancer
|
January 25, 2014
Reduced migration of MLH1 deficient colon cancer cells depends on SPTAN1
Inga Hinrichsen, Benjamin Philipp Ernst, Franziska Nuber, et al.
Molecular Carcinogenesis
|
August 24, 2018
DNA mismatch repair activity of MutLα is regulated by CK2-dependent phosphorylation of MLH1 (S477)
Isabel M Weßbecher, Inga Hinrichsen, Sebastian Funke, et al.
Nucleic Acids Research
|
December 1, 2006
Mutations in the MutSalpha interaction interface of MLH1 can abolish DNA mismatch repair
Guido Plotz, Christoph Welsch, Luis Giron-Monzon, et al.
Nucleic Acids Research
|
May 24, 2023
A conserved motif in the disordered linker of human MLH1 is vital for DNA mismatch repair and its function is diminished by a cancer family mutation
Karla Wolf, Jan Kosinski, Toby J Gibson, et al.
Plos One
|
March 12, 2019
Downregulation of SPTAN1 is related to MLH1 deficiency and metastasis in colorectal cancer
Anne Ackermann, Christopher Schrecker, Dimitra Bon, et al.
Carcinogenesis
|
December 6, 2014
Functional testing strategy for coding genetic variants of unclear significance in MLH1 in Lynch syndrome diagnosis
Inga Hinrichsen, Dieter Schäfer, Deborah Langer, et al.
Human Mutation
|
June 28, 2012
Comprehensive functional assessment of MLH1 variants of unknown significance
Ester Borràs, Marta Pineda, Angela Brieger, et al.
Page
of 5