Cargando…
Tumor suppressor MCPH1 regulates gene expression profiles related to malignant conversion and chromosomal assembly
Strong inherited predisposition to breast cancer is estimated to cause about 5–10% of all breast cancer cases. As the known susceptibility genes, such as BRCA1 and BRCA2, explain only a fraction of this, additional predisposing genes and related biological mechanisms are actively being searched for....
Autores principales: | Tervasmäki, Anna, Mantere, Tuomo, Eshraghi, Leila, Laurila, Niina, Tuppurainen, Hanna, Ronkainen, Veli‐Pekka, Koivuluoma, Susanna, Devarajan, Raman, Peltoketo, Hellevi, Pylkäs, Katri |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6767439/ https://www.ncbi.nlm.nih.gov/pubmed/30809794 http://dx.doi.org/10.1002/ijc.32234 |
Ejemplares similares
-
Targeted Next-Generation Sequencing Identifies a Recurrent Mutation in MCPH1 Associating with Hereditary Breast Cancer Susceptibility
por: Mantere, Tuomo, et al.
Publicado: (2016) -
Evaluating the role of NTHL1 p.Q90* allele in inherited breast cancer predisposition
por: Kumpula, Timo, et al.
Publicado: (2020) -
Truncating TINF2 p.Tyr312Ter variant and inherited breast cancer susceptibility
por: Koivuluoma, Susanna, et al.
Publicado: (2022) -
FANCM c.5101C>T mutation associates with breast cancer survival and treatment outcome
por: Kiiski, Johanna I., et al.
Publicado: (2016) -
Evaluating the role of CHEK2 p.(Asp438Tyr) allele in inherited breast cancer predisposition
por: Kumpula, Timo A., et al.
Publicado: (2023)