IT201700045353A1 - Metodo per la ricerca e l'individuazione di una condizione genetica prodromica all'insorgenza di tumori solidi - Google Patents
Metodo per la ricerca e l'individuazione di una condizione genetica prodromica all'insorgenza di tumori solidiInfo
- Publication number
- IT201700045353A1 IT201700045353A1 IT102017000045353A IT201700045353A IT201700045353A1 IT 201700045353 A1 IT201700045353 A1 IT 201700045353A1 IT 102017000045353 A IT102017000045353 A IT 102017000045353A IT 201700045353 A IT201700045353 A IT 201700045353A IT 201700045353 A1 IT201700045353 A1 IT 201700045353A1
- Authority
- IT
- Italy
- Prior art keywords
- prodromic
- absorbence
- research
- determination
- solid tumors
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
- C12Q1/6876—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
- C12Q1/6883—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
- C12Q1/6886—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material for cancer
-
- G—PHYSICS
- G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
- G16B—BIOINFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR GENETIC OR PROTEIN-RELATED DATA PROCESSING IN COMPUTATIONAL MOLECULAR BIOLOGY
- G16B20/00—ICT specially adapted for functional genomics or proteomics, e.g. genotype-phenotype associations
- G16B20/20—Allele or variant detection, e.g. single nucleotide polymorphism [SNP] detection
-
- G—PHYSICS
- G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
- G16B—BIOINFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR GENETIC OR PROTEIN-RELATED DATA PROCESSING IN COMPUTATIONAL MOLECULAR BIOLOGY
- G16B20/00—ICT specially adapted for functional genomics or proteomics, e.g. genotype-phenotype associations
- G16B20/50—Mutagenesis
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q2600/00—Oligonucleotides characterized by their use
- C12Q2600/156—Polymorphic or mutational markers
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Physics & Mathematics (AREA)
- Genetics & Genomics (AREA)
- Analytical Chemistry (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Biophysics (AREA)
- Molecular Biology (AREA)
- Biotechnology (AREA)
- Wood Science & Technology (AREA)
- Immunology (AREA)
- Zoology (AREA)
- Pathology (AREA)
- Evolutionary Biology (AREA)
- Medical Informatics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Theoretical Computer Science (AREA)
- Bioinformatics & Computational Biology (AREA)
- Microbiology (AREA)
- Hospice & Palliative Care (AREA)
- Oncology (AREA)
- Biochemistry (AREA)
- General Engineering & Computer Science (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
- Investigating Or Analysing Biological Materials (AREA)
- Apparatus Associated With Microorganisms And Enzymes (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Priority Applications (9)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IT102017000045353A IT201700045353A1 (it) | 2017-04-26 | 2017-04-26 | Metodo per la ricerca e l'individuazione di una condizione genetica prodromica all'insorgenza di tumori solidi |
KR1020197034851A KR102507439B1 (ko) | 2017-04-26 | 2017-07-13 | 고형 종양의 개시의 유전적 상태 전구증증을 조사하고 확인하는 방법 |
PCT/IB2017/054231 WO2018197934A1 (en) | 2017-04-26 | 2017-07-13 | Method for searching and identifying a genetic condition prodromal of the onset of solid tumors |
CN201780090026.1A CN110621789A (zh) | 2017-04-26 | 2017-07-13 | 用于搜索和鉴定发生实体瘤的前驱遗传状况的方法 |
EP17780202.2A EP3615682A1 (en) | 2017-04-26 | 2017-07-13 | Method for searching and identifying a genetic condition prodromal of the onset of solid tumors |
JP2019555004A JP6998611B2 (ja) | 2017-04-26 | 2017-07-13 | 固形腫瘍の発症の前駆的遺伝子状態を探索および特定する方法 |
US16/607,993 US20210108270A1 (en) | 2017-04-26 | 2017-07-13 | Method for searching and identifying a genetic condition prodromal of the onset of solid tumors |
SG11201909723T SG11201909723TA (en) | 2017-04-26 | 2017-07-13 | Method for searching and identifying a genetic condition prodromal of the onset of solid tumors |
US17/822,484 US20230124836A1 (en) | 2017-04-26 | 2022-08-26 | System using a method for searching and identifying a genetic condition prodromal of the onset of solid tumors |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IT102017000045353A IT201700045353A1 (it) | 2017-04-26 | 2017-04-26 | Metodo per la ricerca e l'individuazione di una condizione genetica prodromica all'insorgenza di tumori solidi |
Publications (1)
Publication Number | Publication Date |
---|---|
IT201700045353A1 true IT201700045353A1 (it) | 2018-10-26 |
Family
ID=59859466
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
IT102017000045353A IT201700045353A1 (it) | 2017-04-26 | 2017-04-26 | Metodo per la ricerca e l'individuazione di una condizione genetica prodromica all'insorgenza di tumori solidi |
Country Status (8)
Country | Link |
---|---|
US (2) | US20210108270A1 (it) |
EP (1) | EP3615682A1 (it) |
JP (1) | JP6998611B2 (it) |
KR (1) | KR102507439B1 (it) |
CN (1) | CN110621789A (it) |
IT (1) | IT201700045353A1 (it) |
SG (1) | SG11201909723TA (it) |
WO (1) | WO2018197934A1 (it) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20220405917A1 (en) * | 2021-06-18 | 2022-12-22 | Case Western Reserve University | Combination of features from biopsies and scans to predict prognosis in sclc |
WO2023012382A1 (es) * | 2021-08-03 | 2023-02-09 | Genetracer Biotech, S.L. | Método de detección temprana de biomarcadores de tumores sólidos mediante biopsia líquida |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20130143747A1 (en) * | 2011-12-05 | 2013-06-06 | Myriad Genetics, Incorporated | Methods of detecting cancer |
US20160102358A1 (en) * | 2014-10-14 | 2016-04-14 | Wake Forest University Health Sciences | Methods and compositions for correlating genetic markers with cancer risk |
US20160130648A1 (en) * | 2014-11-12 | 2016-05-12 | Neogenomics Laboratories, Inc. | Deep sequencing of peripheral blood plasma dna as a reliable test for confirming the diagnosis of myelodysplastic syndrome |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA2902099C (en) | 2013-03-08 | 2020-06-02 | F. Hoffmann-La Roche Ag | Egfr mutation blood testing |
US10262755B2 (en) * | 2014-04-21 | 2019-04-16 | Natera, Inc. | Detecting cancer mutations and aneuploidy in chromosomal segments |
WO2016127944A1 (en) | 2015-02-10 | 2016-08-18 | The Chinese University Of Hong Kong | Detecting mutations for cancer screening and fetal analysis |
JP6995625B2 (ja) | 2015-05-01 | 2022-01-14 | ガーダント ヘルス, インコーポレイテッド | 診断方法 |
EP3443066A4 (en) * | 2016-04-14 | 2019-12-11 | Guardant Health, Inc. | EARLY DETECTION METHODS FOR CANCER |
-
2017
- 2017-04-26 IT IT102017000045353A patent/IT201700045353A1/it unknown
- 2017-07-13 JP JP2019555004A patent/JP6998611B2/ja active Active
- 2017-07-13 WO PCT/IB2017/054231 patent/WO2018197934A1/en unknown
- 2017-07-13 SG SG11201909723T patent/SG11201909723TA/en unknown
- 2017-07-13 EP EP17780202.2A patent/EP3615682A1/en active Pending
- 2017-07-13 CN CN201780090026.1A patent/CN110621789A/zh active Pending
- 2017-07-13 KR KR1020197034851A patent/KR102507439B1/ko active IP Right Grant
- 2017-07-13 US US16/607,993 patent/US20210108270A1/en not_active Abandoned
-
2022
- 2022-08-26 US US17/822,484 patent/US20230124836A1/en active Pending
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20130143747A1 (en) * | 2011-12-05 | 2013-06-06 | Myriad Genetics, Incorporated | Methods of detecting cancer |
US20160102358A1 (en) * | 2014-10-14 | 2016-04-14 | Wake Forest University Health Sciences | Methods and compositions for correlating genetic markers with cancer risk |
US20160130648A1 (en) * | 2014-11-12 | 2016-05-12 | Neogenomics Laboratories, Inc. | Deep sequencing of peripheral blood plasma dna as a reliable test for confirming the diagnosis of myelodysplastic syndrome |
Non-Patent Citations (3)
Title |
---|
DE MATTOS-ARRUDA LETICIA ET AL: "Cell-free circulating tumour DNA as a liquid biopsy in breast cancer", MOLECULAR ONCOLOGY, ELSEVIER, AMSTERDAM, NL, vol. 10, no. 3, 17 December 2015 (2015-12-17), pages 464 - 474, XP029432258, ISSN: 1574-7891, DOI: 10.1016/J.MOLONC.2015.12.001 * |
JEFFREY GAGAN ET AL: "Next-generation sequencing to guide cancer therapy", GENOME MEDICINE, vol. 7, no. 1, 29 July 2015 (2015-07-29), XP055421971, DOI: 10.1186/s13073-015-0203-x * |
MARK SAUSEN ET AL: "Clinical implications of genomic alterations in the tumour and circulation of pancreatic cancer patients", NATURE COMMUNICATIONS, vol. 6, no. 7686, 7 July 2015 (2015-07-07), pages 1 - 6, XP055326405, DOI: 10.1038/ncomms8686 * |
Also Published As
Publication number | Publication date |
---|---|
JP2020518234A (ja) | 2020-06-25 |
CN110621789A (zh) | 2019-12-27 |
US20230124836A1 (en) | 2023-04-20 |
JP6998611B2 (ja) | 2022-01-18 |
KR20190141236A (ko) | 2019-12-23 |
US20210108270A1 (en) | 2021-04-15 |
WO2018197934A1 (en) | 2018-11-01 |
KR102507439B1 (ko) | 2023-03-08 |
SG11201909723TA (en) | 2019-11-28 |
EP3615682A1 (en) | 2020-03-04 |
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