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Author/Creator Hinrichsen, Inga

1. Comprehensive Functional Assessment of MLH1 Variants of Unknown Significance. Issue 1 (27th November 2012)

Authors:
Borràs, Ester; Pineda, Marta; Brieger, Angela; Hinrichsen, Inga; Gómez, Carolina; Navarro, Matilde; Balmaña, Judit; Ramón y Cajal, Teresa; Torres, Asunción; Brunet, Joan; Blanco, Ignacio; Plotz, Guido; Lázaro, Conxi; Capellá, Gabriel
Journal:
Human mutation
Issue:
Volume 34:Issue 1(2013:Jan.)
Page Start:
274
Record Type:
Journal Article
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2. DNA mismatch repair activity of MutLα is regulated by CK2‐dependent phosphorylation of MLH1 (S477). Issue 12 (5th September 2018)

Authors:
Weßbecher, Isabel M.; Hinrichsen, Inga; Funke, Sebastian; Oellerich, Thomas; Plotz, Guido; Zeuzem, Stefan; Grus, Franz H.; Biondi, Ricardo M.; Brieger, Angela
Journal:
Molecular carcinogenesis
Issue:
Volume 57:Issue 12(2018)
Page Start:
1723
Record Type:
Journal Article
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3. Evaluation of MLH1 variants of unclear significance. Issue 7 (30th April 2018)

Authors:
Köger, Nicole; Paulsen, Lea; López‐Kostner, Francisco; Della Valle, Adriana; Vaccaro, Carlos Alberto; Palmero, Edenir Inêz; Alvarez, Karin; Sarroca, Carlos; Neffa, Florencia; Kalfayan, Pablo German; Gonzalez, Maria Laura; Rossi, Benedito Mauro; Reis, Rui Manuel; Brieger, Angela; Zeuzem, Stefan; H...
Journal:
Genes, chromosomes & cancer
Issue:
Volume 57:Issue 7(2018)
Page Start:
350
Record Type:
Journal Article
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6. Refining the role of pms2 in Lynch syndrome: germline mutational analysis improved by comprehensive assessment of variants. Issue 8 (24th May 2013)

Authors:
Borràs, Ester; Pineda, Marta; Cadiñanos, Juan; del Valle, Jesús; Brieger, Angela; Hinrichsen, Inga; Cabanillas, Ruben; Navarro, Matilde; Brunet, Joan; Sanjuan, Xavier; Musulen, Eva; van der Klift, Helen; Lázaro, Conxi; Plotz, Guido; Blanco, Ignacio; Capellá, Gabriel
Journal:
Journal of medical genetics
Issue:
Volume 50:Issue 8(2013)
Page Start:
552
Record Type:
Journal Article
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