Found: 19
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The detection of isochromosome i(12p) in malignant germ cell tumours and tumours with somatic malignant transformation by the use of quantitative real‐time polymerase chain reaction.
- Published in:
- Histopathology, 2021, v. 78, n. 4, p. 593, doi. 10.1111/his.14258
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- Publication type:
- Article
TP53 -Status-Dependent Oncogenic EZH2 Activity in Pancreatic Cancer.
- Published in:
- Cancers, 2022, v. 14, n. 14, p. N.PAG, doi. 10.3390/cancers14143451
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- Publication type:
- Article
Expansion of the complex genotypic and phenotypic spectrum of FGFR2-associated neurocutaneous syndromes.
- Published in:
- Human Genetics, 2024, v. 143, n. 2, p. 159, doi. 10.1007/s00439-023-02634-1
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- Publication type:
- Article
Germline loss-of-function variants in the BARD1 gene are associated with early-onset familial breast cancer but not ovarian cancer.
- Published in:
- 2019
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- Publication type:
- journal article
Phytoestrogens from Belamcanda chinensis regulate the expression of steroid receptors and related cofactors in LNCaP prostate cancer cells.
- Published in:
- BJU International, 2007, v. 100, n. 1, p. 199, doi. 10.1111/j.1464-410X.2007.06924.x
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- Publication type:
- Article
Evidence of Two Novel LAMA2 Variants in a Patient With Muscular Dystrophy: Facing the Challenges of a Certain Diagnosis.
- Published in:
- Frontiers in Neurology, 2022, v. 13, p. 1, doi. 10.3389/fneur.2022.893605
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- Publication type:
- Article
Amygdalin Influences Bladder Cancer Cell Adhesion and Invasion In Vitro.
- Published in:
- PLoS ONE, 2014, v. 9, n. 10, p. 1, doi. 10.1371/journal.pone.0110244
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- Publication type:
- Article
Amygdalin Blocks Bladder Cancer Cell Growth <i>In Vitro</i> by Diminishing Cyclin A and cdk2.
- Published in:
- PLoS ONE, 2014, v. 9, n. 8, p. 1, doi. 10.1371/journal.pone.0105590
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- Publication type:
- Article
Mutations in the cyclin family member FAM58A cause an X-linked dominant disorder characterized by syndactyly, telecanthus and anogenital and renal malformations.
- Published in:
- Nature Genetics, 2008, v. 40, n. 3, p. 287, doi. 10.1038/ng.86
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- Publication type:
- Article
Leupaxin is expressed in mammary carcinoma and acts as a transcriptional activator of the estrogen receptor α.
- Published in:
- International Journal of Oncology, 2015, v. 47, n. 1, p. 106, doi. 10.3892/ijo.2015.2988
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- Publication type:
- Article
Increased microtubule assembly rates influence chromosomal instability in colorectal cancer cells.
- Published in:
- Nature Cell Biology, 2014, v. 16, n. 8, p. 779, doi. 10.1038/ncb2994
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- Publication type:
- Article
Survey of germline variants in cancer‐associated genes in young adults with colorectal cancer.
- Published in:
- Genes, Chromosomes & Cancer, 2022, v. 61, n. 2, p. 105, doi. 10.1002/gcc.23011
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- Publication type:
- Article
PIK3CA mutations are specifically localized to lymphatic endothelial cells of lymphatic malformations.
- Published in:
- PLoS ONE, 2018, v. 13, n. 7, p. 1, doi. 10.1371/journal.pone.0200343
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- Publication type:
- Article
Moebius syndrome and gastroschisis—The second case of a rare association.
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- American Journal of Medical Genetics. Part A, 2024, v. 194, n. 1, p. 111, doi. 10.1002/ajmg.a.63411
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- Publication type:
- Article
Aplasia cutis congenita in a CDC42‐related developmental phenotype.
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- American Journal of Medical Genetics. Part A, 2021, v. 185, n. 3, p. 850, doi. 10.1002/ajmg.a.62009
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- Publication type:
- Article
Valproic acid inhibits the proliferation of cancer cells by re-expressing cyclin D2.
- Published in:
- Carcinogenesis, 2013, v. 34, n. 5, p. 1115, doi. 10.1093/carcin/bgt019
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- Publication type:
- Article
Progressive frontal intraosseous lipoma: Detection of the mosaic AKT1 variant discloses Proteus syndrome.
- Published in:
- Clinical Genetics, 2022, v. 102, n. 3, p. 239, doi. 10.1111/cge.14174
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- Publication type:
- Article
Phenotypic spectrum of BLM- and RMI1-related Bloom syndrome.
- Published in:
- Clinical Genetics, 2022, v. 101, n. 5/6, p. 559, doi. 10.1111/cge.14125
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- Publication type:
- Article
RNF43 pathogenic Germline variant in a family with colorectal cancer.
- Published in:
- Clinical Genetics, 2022, v. 101, n. 1, p. 122, doi. 10.1111/cge.14064
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- Publication type:
- Article