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A high-throughput screen to identify novel synthetic lethal compounds for the treatment of E-cadherin-deficient cells.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-48929-0
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- Publication type:
- Article
Association of CDH1 haplotypes with susceptibility to sporadic diffuse gastric cancer.
- Published in:
- Oncogene, 2002, v. 21, n. 53, p. 8192, doi. 10.1038/sj.onc.1205921
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- Publication type:
- Article
Germline E-cadherin gene mutations.
- Published in:
- Cancer (0008543X), 2001, v. 92, n. 1, p. 181, doi. 10.1002/1097-0142(20010701)92:1<181::AID-CNCR1307>3.0.CO;2-J
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- Publication type:
- Article
Blending space and time to talk about cancer in extended reality.
- Published in:
- NPJ Digital Medicine, 2024, v. 7, n. 1, p. 1, doi. 10.1038/s41746-024-01262-x
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- Publication type:
- Article
Analytical Validation of Cxbladder ® Detect, Triage, and Monitor: Assays for Detection and Management of Urothelial Carcinoma.
- Published in:
- Diagnostics (2075-4418), 2024, v. 14, n. 18, p. 2061, doi. 10.3390/diagnostics14182061
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- Publication type:
- Article
Familial gastric cancer: clinicopathological characteristics, RER phenotype and germline p53 and E-cadherin mutations.
- Published in:
- Carcinogenesis, 1999, v. 20, n. 6, p. 1127, doi. 10.1093/carcin/20.6.1127
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- Publication type:
- Article
Dynamic ctDNA Mutational Complexity in Patients with Melanoma Receiving Immunotherapy.
- Published in:
- Molecular Diagnosis & Therapy, 2023, v. 27, n. 4, p. 537, doi. 10.1007/s40291-023-00651-4
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- Publication type:
- Article
Epigenetic silencing in non-neoplastic epithelia identifies E-cadherin ( CDH1) as a target for chemoprevention of lobular neoplasia.
- Published in:
- Journal of Pathology, 2009, v. 218, n. 2, p. 265, doi. 10.1002/path.2541
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- Publication type:
- Article
E-Cadherin-Deficient Cells Are Sensitive to the Multikinase Inhibitor Dasatinib.
- Published in:
- Cancers, 2022, v. 14, n. 7, p. 1609, doi. 10.3390/cancers14071609
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- Publication type:
- Article
E-Cadherin-Deficient Epithelial Cells Are Sensitive to HDAC Inhibitors.
- Published in:
- Cancers, 2022, v. 14, n. 1, p. 175, doi. 10.3390/cancers14010175
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- Publication type:
- Article
Loss of E-Cadherin Leads to Druggable Vulnerabilities in Sphingolipid Metabolism and Vesicle Trafficking.
- Published in:
- Cancers, 2022, v. 14, n. 1, p. 102, doi. 10.3390/cancers14010102
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- Publication type:
- Article
Allosteric AKT Inhibitors Target Synthetic Lethal Vulnerabilities in E-Cadherin-Deficient Cells.
- Published in:
- Cancers, 2019, v. 11, n. 9, p. 1359, doi. 10.3390/cancers11091359
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- Publication type:
- Article
Modelling hereditary diffuse gastric cancer initiation using transgenic mouse‐derived gastric organoids and single‐cell sequencing.
- Published in:
- Journal of Pathology, 2021, v. 254, n. 3, p. 254, doi. 10.1002/path.5675
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- Publication type:
- Article
E-cadherin loss alters cytoskeletal organization and adhesion in non-malignant breast cells but is insufficient to induce an epithelial-mesenchymal transition.
- Published in:
- 2014
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- Publication type:
- journal article
A novel diffuse gastric cancer susceptibility variant in E-cadherin (CDH1) intron 2: a case control study in an Italian population.
- Published in:
- 2008
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- Publication type:
- journal article
A novel diffuse gastric cancer susceptibility variant in E-cadherin (CDH1) intron 2: A case control study in an Italian population.
- Published in:
- BMC Cancer, 2008, v. 8, p. 1, doi. 10.1186/1471-2407-8-138
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- Publication type:
- Article
Hereditary diffuse gastric cancer: A manifestation of lost cell polarity.
- Published in:
- Cancer Science, 2009, v. 100, n. 7, p. 1151, doi. 10.1111/j.1349-7006.2009.01163.x
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- Publication type:
- Article
Novel germline CDH1 mutations in hereditary diffuse gastric cancer families.
- Published in:
- Human Mutation, 2002, v. 19, n. 5, p. 518, doi. 10.1002/humu.10067
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- Publication type:
- Article
E-cadherin germline mutations define an inherited cancer syndrome dominated by diffuse gastric cancer.
- Published in:
- Human Mutation, 1999, v. 14, n. 3, p. 249, doi. 10.1002/(SICI)1098-1004(1999)14:3<249::AID-HUMU8>3.0.CO;2-9
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- Publication type:
- Article
Expression of Krüppel-like factor 5 in human gastric carcinomas.
- Published in:
- Journal of Cancer Research & Clinical Oncology, 2008, v. 134, n. 2, p. 163, doi. 10.1007/s00432-007-0265-2
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- Publication type:
- Article
Circulating tumor DNA is a sensitive marker for routine monitoring of treatment response in advanced colorectal cancer.
- Published in:
- Carcinogenesis, 2020, v. 41, n. 11, p. 1507, doi. 10.1093/carcin/bgaa102
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- Publication type:
- Article
E-cadherin loss alters cytoskeletal organization and adhesion in non-malignant breast cells but is insufficient to induce an epithelial-mesenchymal transition.
- Published in:
- BMC Cancer, 2014, v. 14, p. 1, doi. 10.1186/1471-2407-14-552
- By:
- Publication type:
- Article
E-cadherin loss alters cytoskeletal organization and adhesion in non-malignant breast cells but is insufficient to induce an epithelial-mesenchymal transition.
- Published in:
- BMC Cancer, 2014, v. 14, n. 1, p. 552, doi. 10.1186/1471-2407-14-552
- By:
- Publication type:
- Article
E-cadherin germline mutations in familial gastric cancer.
- Published in:
- Nature, 1998, v. 392, n. 6674, p. 402, doi. 10.1038/32918
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- Publication type:
- Article
An estimate of limited duration cancer prevalence in New Zealand using 'big' data.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Where to from here? Posthumous healthcare data, digital e(lectronic)-mortality and New Zealand's healthcare future.
- Published in:
- 2017
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- Publication type:
- journal article
Methylation of the CDH1 promoter as the second genetic hit in hereditary diffuse gastric cancer.
- Published in:
- Nature Genetics, 2000, v. 26, n. 1, p. 16, doi. 10.1038/79120
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- Publication type:
- Article
E-cadherin-deficient cells have synthetic lethal vulnerabilities in plasma membrane organisation, dynamics and function.
- Published in:
- Gastric Cancer, 2019, v. 22, n. 2, p. 273, doi. 10.1007/s10120-018-0859-1
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- Publication type:
- Article
Hereditary diffuse gastric cancer: translation of CDH1 germline mutations into clinical practice.
- Published in:
- Gastric Cancer, 2010, v. 13, n. 1, p. 1, doi. 10.1007/s10120-009-0531-x
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- Publication type:
- Article
Genomic characterization of multiple clinical phenotypes of cancer using multivariate linear regression models.
- Published in:
- Bioinformatics, 2007, v. 23, n. 6, p. 732, doi. 10.1093/bioinformatics/btl663
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- Publication type:
- Article
Hereditary gastric cancer: what's new? Update 2013–2018.
- Published in:
- Familial Cancer, 2019, v. 18, n. 3, p. 363, doi. 10.1007/s10689-019-00127-7
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- Publication type:
- Article
Germline CDH1 mutations are a significant contributor to the high frequency of early-onset diffuse gastric cancer cases in New Zealand Māori.
- Published in:
- Familial Cancer, 2019, v. 18, n. 1, p. 83, doi. 10.1007/s10689-018-0080-8
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- Publication type:
- Article
ASO Visual Abstract: Disappearing Signet Ring Cell Adenocarcinoma in Gastric Cancer Patients.
- Published in:
- 2024
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- Publication type:
- Abstract
Disappearing Signet Ring Cell Adenocarcinoma in Gastric Cancer Patients.
- Published in:
- Annals of Surgical Oncology: An Oncology Journal for Surgeons, 2024, v. 31, n. 13, p. 9030, doi. 10.1245/s10434-024-16117-8
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- Publication type:
- Article
Risk of stomach cancer in Aotearoa/New Zealand: A Māori population based case-control study.
- Published in:
- PLoS ONE, 2017, v. 12, n. 7, p. 1, doi. 10.1371/journal.pone.0181581
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- Publication type:
- Article
E-cadherin signal sequence disruption: a novel mechanism underlying hereditary cancer.
- Published in:
- Molecular Cancer, 2018, v. 17, n. 1, p. N.PAG, doi. 10.1186/s12943-018-0859-0
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- Publication type:
- Article
Identification of c.1531C>T Pathogenic Variant in the CDH1 Gene as a Novel Germline Mutation of Hereditary Diffuse Gastric Cancer.
- Published in:
- International Journal of Molecular Sciences, 2019, v. 20, n. 20, p. 4980, doi. 10.3390/ijms20204980
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- Publication type:
- Article
Cohesin mutations are synthetic lethal with stimulation of WNT signaling.
- Published in:
- eLife, 2020, p. 1, doi. 10.7554/eLife.61405
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- Publication type:
- Article
A gene responsible for a dominant form of neurosensory non-syndromic deafness maps to the NSRD1 recessive deafness gene interval.
- Published in:
- Human Molecular Genetics, 1994, v. 3, n. 12, p. 2219
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- Publication type:
- Article
A human gene responsible for neurosensory, non-syndromic recessive deafness is a candidate homologue of the mouse sh-1 gene.
- Published in:
- Human Molecular Genetics, 1994, v. 3, n. 6, p. 989
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- Publication type:
- Article
Genome-wide methylation analysis identifies a core set of hypermethylated genes in CIMP-H colorectal cancer.
- Published in:
- 2017
- By:
- Publication type:
- journal article