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Bibliografías temáticas / Consensus mutation

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Literatura académica sobre el tema "Consensus mutation"

Autor: Grafiati

Publicado: 1 de febrero de 2025

Última modificación: 31 de julio de 2025

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Artículos de revistas sobre el tema "Consensus mutation"

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Graña, D., T. Gardella, and M. M. Susskind. "The effects of mutations in the ant promoter of phage P22 depend on context." Genetics 120, no. 2 (1988): 319–27. http://dx.doi.org/10.1093/genetics/120.2.319.

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Abstract Recombination was used to construct 22 two- or three-way combinations of down- and up-mutations in Pant, a strong, near-consensus promoter of phage P22. The relative strengths of these promoters in vivo were assayed by fusing them to an ant/lacZ gene fusion and measuring beta-galactosidase levels produced by lysogens carrying the fusions on single-copy prophages. The results of these assays show that the magnitude of the effect of a promoter mutation can vary considerably when its context is changed by the presence of another mutation. In addition, as Pant approaches conformity with t

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Parikh, Purvish M., J. Wadhwa, S. Minhas, et al. "Practical consensus recommendation on when to do BRCA testing." South Asian Journal of Cancer 07, no. 02 (2018): 106. http://dx.doi.org/10.4103/sajc.sajc_112_18.

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Abstract BRCA-mutation associated breast cancer and to future cancer risks and sensitivity to systemic therapies. Now that rapid genetic testing for BRCA1 and BRCA2 mutations is available, BRCA mutation status can be considered when making treatment and prevention decisions for BRCA testing, BRCA mutation carriers with breast cancer. Expert group used data from published literature, practical experience, and opinion of a large group of academic oncologists, to arrive at practical consensus recommendations for use by the community oncologists.

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Dong, Baijun, Bin Yang, Yonghong Li, et al. "Insights into Chinese prostate cancer germline gene mutation profile: HOXB13 G84E mutation is unsuitable for genetic testing." Journal of Clinical Oncology 38, no. 15_suppl (2020): e17515-e17515. http://dx.doi.org/10.1200/jco.2020.38.15_suppl.e17515.

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e17515 Background: Philadelphia Prostate Cancer Consensus Conference 2017 developed an expert consensus-driven working framework for comprehensive genetic evaluation of inherited PCA. However, the consensus was mainly based on data from Caucasian populations. Genetic differences in the PC molecular landscape between Asian and Caucasian men have been established. Whether Caucasian-based genetic information can be used to guide clinical practice in Chinese population needs further evidence. Methods: 1123 patients with confirmed prostate cancer admitted from March 2018 to August 2019 from 18 Chin

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Bergeron, Julie, Jose-Mario Capo-Chichi, Hubert Tsui, et al. "The Clinical Utility of FLT3 Mutation Testing in Acute Leukemia: A Canadian Consensus." Current Oncology 30, no. 12 (2023): 10410–36. http://dx.doi.org/10.3390/curroncol30120759.

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FMS-like tyrosine kinase 3 (FLT3) mutations are detected in approximately 20–30% of patients with acute myeloid leukemia (AML), with the presence of a FLT3 internal tandem duplication (FLT3-ITD) mutation being associated with an inferior outcome. Assessment of FLT3 mutational status is now essential to define optimal upfront treatment in both newly diagnosed and relapsed AML, to support post-induction allogeneic hematopoietic stem cell transplantation (alloSCT) decision-making, and to evaluate treatment response via measurable (minimal) residual disease (MRD) evaluation. In view of its importa

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Amar, Laurence, Karel Pacak, Olivier Steichen, et al. "International consensus on initial screening and follow-up of asymptomatic SDHx mutation carriers." Nature Reviews Endocrinology 17, no. 7 (2021): 435–44. http://dx.doi.org/10.1038/s41574-021-00492-3.

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AbstractApproximately 20% of patients diagnosed with a phaeochromocytoma or paraganglioma carry a germline mutation in one of the succinate dehydrogenase (SDHx) genes (SDHA, SDHB, SDHC and SDHD), which encode the four subunits of the SDH enzyme. When a pathogenic SDHx mutation is identified in an affected patient, genetic counselling is proposed for first-degree relatives. Optimal initial evaluation and follow-up of people who are asymptomatic but might carry SDHx mutations have not yet been agreed. Thus, we established an international consensus algorithm of clinical, biochemical and imaging

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Breitschwerdt, Sven, Benedikt Grandel, Benedikt Asbach, et al. "Consensus Sequences for Gag and Pol Introduced into HIV-1 Clade B Laboratory Strains Differentially Influence the Impact of Point Mutations Associated with Immune Escape and with Drug Resistance on Viral Replicative Capacity." Viruses 17, no. 6 (2025): 842. https://doi.org/10.3390/v17060842.

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Viral evasion from effective human immunodeficiency virus type 1 (HIV-1)-specific CD8+ T-cell responses and from antiretroviral therapy through viral sequence variation is frequently accompanied by a loss in viral fitness. The impact of sequence variations on replication capacity in vitro was mostly studied by introducing single mutations into a specific clonal strain such as NL4-3. How the specific viral backbone itself impacts replicative fitness remains elusive. To test for a potential effect of the viral backbone, we constructed HIV-1 clade B clones with consensus sequences for gag and/or

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Kipling, D., and S. E. Kearsey. "Reversion of autonomously replicating sequence mutations in Saccharomyces cerevisiae: creation of a eucaryotic replication origin within procaryotic vector DNA." Molecular and Cellular Biology 10, no. 1 (1990): 265–72. http://dx.doi.org/10.1128/mcb.10.1.265-272.1990.

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To investigate how a defective replicon might acquire replication competence, we have studied the reversion of autonomously replicating sequence (ARS) mutations. By mutagenesis of a Saccharomyces cerevisiae plasmid lacking a functional origin of replication, we have obtained a series of cis-acting mutations which confer ARS activity on the plasmid. The original plasmid contained an ARS element inactivated by point mutation, but surprisingly only 1 of the 10 independent Ars+ revertants obtained shows a back mutation in this element. In the remainder of the revertants, sequence changes in the M1

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Kipling, D., and S. E. Kearsey. "Reversion of autonomously replicating sequence mutations in Saccharomyces cerevisiae: creation of a eucaryotic replication origin within procaryotic vector DNA." Molecular and Cellular Biology 10, no. 1 (1990): 265–72. http://dx.doi.org/10.1128/mcb.10.1.265.

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To investigate how a defective replicon might acquire replication competence, we have studied the reversion of autonomously replicating sequence (ARS) mutations. By mutagenesis of a Saccharomyces cerevisiae plasmid lacking a functional origin of replication, we have obtained a series of cis-acting mutations which confer ARS activity on the plasmid. The original plasmid contained an ARS element inactivated by point mutation, but surprisingly only 1 of the 10 independent Ars+ revertants obtained shows a back mutation in this element. In the remainder of the revertants, sequence changes in the M1

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Baer, Constance Regina, Niroshan Nadarajah, Claudia Haferlach, Wolfgang Kern, and Torsten Haferlach. "The Use of Unique Molecular Identifiers (UMIs) Strongly Improves Sequencing Detection Limits Allowing Earlier Detection of Small TP53 Mutated Clones in Leukemias." Blood 128, no. 22 (2016): 2027. http://dx.doi.org/10.1182/blood.v128.22.2027.2027.

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Abstract Background: TP53 mutations arise in a broad set of hematologic diseases and are associated with poor prognosis and therapy failure. Even small TP53 mutated clones were demonstrated to be of clinical relevance and therefore their early detection is mandatory. Mutations can occur throughout the entire gene (mainly exons 4-10) and include base exchanges, deletions and insertions. Next generation sequencing (NGS) generally detects mutations, which are present in at least 3% of sequences. The detection of mutations at burdens below 3% is still hampered by polymerase and sequencing errors.

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Yuryev, Anton, and Jeffry L. Corden. "Suppression Analysis Reveals a Functional Difference Between the Serines in Positions Two and Five in the Consensus Sequence of the C-Terminal Domain of Yeast RNA Polymerase II." Genetics 143, no. 2 (1996): 661–71. http://dx.doi.org/10.1093/genetics/143.2.661.

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Abstract The largest subunit of RNA polymerase II contains a repetitive C-terminal domain (CTD) consisting of tandem repeats of the consensus sequence TyrlSer2Pro3Thr4Ser5Pro6Ser7. Substitution of nonphosphe rylatable amino acids at positions two or five of the Saccharomyces cerevisiae CTD is lethal. We developed a selection ssytem for isolating suppressors of this lethal phenotype and cloned a gene, SCA1 (suppressor of CTD alanine), which complements recessive suppressors of lethal multiple-substitution mutations. A partial deletion of SCA1 (sca1Δ::hisG) suppresses alanine or glutamate substi

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Tesis sobre el tema "Consensus mutation"

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Callahan, Nicholas. "Bioinformatics-Driven Enzyme Engineering: Work On Adenylate Kinase." The Ohio State University, 2015. http://rave.ohiolink.edu/etdc/view?acc_num=osu1420802270.

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Jamal, Layal. "Structural and functional characterization of the lysosomal amino acid transporter PQLC2." Electronic Thesis or Diss., université Paris-Saclay, 2024. http://www.theses.fr/2024UPASL129.

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PQLC2, qui signifie protéine conte- nant des répétitions de boucle proline-glutamine 2, appartient à une famille de protéines de transport membranaires caractérisées par une topologie membranaire à sept hélices et deux motifs proline-glutamine. PQLC2 est localisé dans la membrane lysosomale des cellules mammifères, et des études utilisant du PQLC2 recombinant exprimé dans des ovocytes de Xenopus ont démontré que PQLC2 est un uniporteur qui transporte spécifiquement des acides aminés cationiques. Cependant, sa structure atomique en 3D n’a pas encore été déterminée. En plus de son rôle de transp

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Mok, Chee-Keng, and 莫子京. "Alanine-Scanning Mutations in Consensus Regions of Influenza A Virus Neuraminidase." Thesis, 2007. http://ndltd.ncl.edu.tw/handle/jr4hg7.

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碩士<br>長庚大學<br>醫學生物技術研究所<br>95<br>Neuraminidase (NA), a surface glycoprotein of Influenza A virus, is an important molecular target in the development of antiviral drugs. Twenty-eight highly conserved amino acid residues in influenza A viral NA protein were identified through in silico analysis based on 2,827 NA sequences deposited in NCBI. Seven out of 28 are located on the site of sialic acid interactions of NA. Positions 151 and 371 have been reported to influence the susceptibility of drugs to Tamiflu or Zanamivir. With an A/WSN/33 (H1N1) as a backbone, alanine substitution was introduced i

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Hu, Rei-Hsing, and 胡瑞興. "Mutational effects of the consensus aromatic residues in the mRNA capping domain of Bamboo mosaic virus on GTP methylation and virus accumulation and the establishment of BaMV replication system in Saccharomyces cerevisiae." Thesis, 2011. http://ndltd.ncl.edu.tw/handle/10072744641647859348.

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博士<br>國立中興大學<br>生物科技學研究所<br>99<br>Bamboo mosaic virus (BaMV), a member of the Potexvirus of the alpaviurslike superfamily, is a positive-strand RNA virus. The genome of BaMV consists of five open reading frames (ORFs), and the ORF 1 encodes a 155-kDa replicase, which could be separated into a capping enzyme domain, a helicase-like domain (HLD), and an RNA-dependent RNA polymerase domain (RdRp) from N to C terminus. The alphavirus-like superfamily has a special pathway for cap formation, by which the capping enzyme will first methylate GTP to generate m7GTP (methyltransferase activity) and tran

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Capítulos de libros sobre el tema "Consensus mutation"

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Sieradzka, Katarzyna, Kinga Leszczorz, Mateusz Garbulowski, and Andrzej Polanski. "Consensus Approach for Detection of Cancer Somatic Mutations." In Advances in Intelligent Systems and Computing. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-67792-7_17.

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Muller, Ulrich. "MSX2 and ALX4 and Craniosynostosis and Defects of Skull Ossification." In Inborn Errors Of Development. Oxford University PressNew York, NY, 2008. http://dx.doi.org/10.1093/oso/9780195306910.003.0076.

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Abstract Mutations in the homeobox gene MSX2 can result in both craniosynostosis (premature fusion of the calvarial sutures) and its opposite, parietal foramina (PFM) (delayed ossification along the sagittal sutures). The one MSX2 mutation (Pro148His) described in craniosynostosis to date results in a gain of gene function due to increased binding to the consensus MSX binding site and the subsequent overstimulation of MSX2 target genes. Conversely, haploinsufficiency of MSX2 is the cause of PFM. Haploinsufficiency of another homeobox gene, ALX4, can also underlie PFM. No mutation has yet been

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Lopes, Luis Rocha. "Dilated cardiomyopathy: genetics." In ESC CardioMed. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198784906.003.0355.

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The genetic background of dilated cardiomyopathy is characterized by heterogeneity. Truncating mutations in titin (TTN), responsible for around 20% of cases, have recently been recognized as the most prevalent genetic cause of dilated cardiomyopathy. Other important causal genes are LMNA (coding for the nuclear envelope protein, lamin A/C) and sarcomere protein genes, such as beta-myosin heavy chain (MYH7) and troponin T (TNNT2). Other loci, including genes that code for cytoskeleton, Z-disc, and membrane-associated proteins, are each responsible for a lower percentage of cases. Current consen

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Lank, David B. "Synthesis and conclusions." In The Snow Geese Of La Pérouse Bay. Oxford University PressOxford, 1995. http://dx.doi.org/10.1093/oso/9780198540649.003.0014.

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Abstract About half a century ago, biologists reached a broad consensus that four fundamental processes could account for evolutionary change within populations. Natural selection, gene flow, genetic drift, and the generation of new variability through mutation were recognized as the major processes moulding the genetic variation of populations. Since that consensus, ecological geneticists and others have tried to determine precisely how these sources of genetic stability and change have interacted to determine the current evolutionary status of populations and might operate in the future to d

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Schnapf Bruce and Farrell Philip. "Cystic Fibrosis." In Metabolic Diseases. IOS Press, 2017. https://doi.org/10.3233/978-1-61499-718-4-511.

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Cystic fibrosis (CF) is an inherited autosomal recessive disorder that is associated with chronic multi-organ disease. Recurrent sinopulmonary infections, nutritional abnormalities, and malabsorption serve as a hallmark of most of the morbidity and mortality. Major advances into the understanding of the pathophysiology has led directly to improvement in survival and quality of life. Today, CF is most commonly diagnosed through newborn screening. Newer therapies that serve as CF transmembrane conductance regulator (CFTR) modulators are able to target the basic defect of CF. CFTR mutations are c

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Burling, Robbins. "The Slow Growth of Language in Children." In The Transition to Language. Oxford University PressOxford, 2002. http://dx.doi.org/10.1093/oso/9780199250653.003.0014.

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Abstract A surprisingly broad consensus has grown among scholars who are interested in the origin of language that the ability to speak was a relatively recent and quite rapid development (e.g. Noble and Davidson 1996: 17). Hardly anyone would now go so far as to credit a single mutation for all syntax, as Bickerton once did (1990, 1998), and even Bickerton has moderated his earlier position (Bickerton 2000, Calvin and Bickerton 2000). Carstairs Mc Carthy has also proposed a scenario that allows for more than a single stage of syntax (1999, 2000). In spite of this, however, full syntax is stil

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Arbustini, Eloisa, Valentina Favalli, Alessandro Di Toro, Alessandra Serio, and Jagat Narula. "Classification of cardiomyopathies." In ESC CardioMed. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198784906.003.0348_update_001.

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For over 50 years, the definition and classification of cardiomyopathies have remained anchored in the concept of ventricular dysfunction and myocardial structural remodelling due to unknown cause. The concept of idiopathic was first challenged in 2006, when the American Heart Association classification subordinated the phenotype to the aetiology. Cardiomyopathies were classified as genetic, acquired, and mixed. In 2008, the European Society of Cardiology proposed a phenotype-driven classification that separated familial (genetic) from non-familial (non-genetic) forms of cardiomyopathy. Both c

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Hamblin, Jacob Darwin. "A Thousand Years into One." In The Wretched Atom. Oxford University Press, 2021. http://dx.doi.org/10.1093/oso/9780197526903.003.0003.

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Eisenhower’s “Atoms for Peace” speech is often seen as the founding story of atomic energy’s peaceful side. In fact, it was not such a dramatic break from the past. The Democrats had begun to use the atom in this way, first with radioisotopes and then with other intriguing ideas, such as irradiating seeds in the hope of generating wondrous mutations. The Democrats hatched the germ of the idea of “Atoms for Peace,” calling for a global atomic Marshall Plan, shortly after President Truman announced in 1949 his decision to pursue development of the hydrogen bomb. The idea of the peaceful atom was

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Basso, Cristina, Hugh Calkins, and Domenico Corrado. "Arrhythmogenic right ventricular cardiomyopathy." In The ESC Textbook of Heart Failure, edited by Petar M. Seferović, Andrew J. S. Coats, Gerasimos Filippatos, Stefan D. Anker, Johann Bauersachs, and Giuseppe Rosano. Oxford University PressOxford, 2023. http://dx.doi.org/10.1093/med/9780198891628.003.0010.

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Abstract Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a heredo-familial heart muscle disease characterized by progressive myocardial atrophy with fibrofatty replacement. It is a rare disease with an estimated prevalence of 1:2000 to 1:5000. Pathogenic mutations are identified in about 50% of probands, mostly in genes encoding desmosomal proteins. ARVC is a major cause of life-threatening ventricular arrhythmias at risk of sudden death in the young. A less common presentation is heart failure mimicking dilated cardiomyopathy. Risk stratification is a major clinical challenge, and s

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M. Harvey, Evan, Murad Almasri, and Hugo R. Martinez. "Genetics of Cardiomyopathy." In Cardiomyopathy - Disease of the Heart Muscle [Working Title]. IntechOpen, 2021. http://dx.doi.org/10.5772/intechopen.97010.

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Cardiomyopathies (CMs) encompass a heterogeneous group of structural and functional (systolic and diastolic) abnormalities of the myocardium and are either confined to the cardiovascular system or are part of a systemic disorder. CMs represent a leading cause of morbidity and mortality and account for a significant percentage of death and cardiac transplantation. The 2006 American Heart Association (AHA) classification grouped CMs into primary (genetic, mixed, or acquired) or secondary (i.e., infiltrative or autoimmune). In 2008, the European Society of Cardiology classification proposed subgr

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Actas de conferencias sobre el tema "Consensus mutation"

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Hamza, Noha M., Daryl L. Essam, and Ruhul A. Sarker. "Differential evolution with a constraint consensus mutation for solving optimization problems." In 2014 IEEE Congress on Evolutionary Computation (CEC). IEEE, 2014. http://dx.doi.org/10.1109/cec.2014.6900474.

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Da Silva, José Eduardo H., Francisco A. L. Manfrini, Heder S. Bernardino, and Helio J. C. Barbosa. "Biased Mutation and Tournament Selection Approaches for Designing Combinational Logic Circuits via Cartesian Genetic Programming." In XV Encontro Nacional de Inteligência Artificial e Computacional. Sociedade Brasileira de Computação - SBC, 2018. http://dx.doi.org/10.5753/eniac.2018.4471.

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Cartesian Genetic Programming (CGP) is often applied to design combinational logic circuits. However, there is no consensus in the literature regarding the more appropriate objective function when it is desired to minimize the number of logic gates of the circuit. Thus, we analyze here two strategies: the minimization of the number of logic gates and the maximization of the number of wire gates. Additionally, a biased mutation strategy for CGP, which were previously presented and tested only to find a feasible solution, are extended in this paper for the subsequent optimization step. Several c

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Assunção, Silvaleide Ataides, Vinicius Lemos Nascimento, Bruno Henrique de Aguiar Brito, et al. "NTRK MUTATION IN ADENOID CYSTIC CARCINOMA: A RARE TYPE OF TRIPLE NEGATIVE." In Abstracts from the Brazilian Breast Cancer Symposium - BBCS 2021. Mastology, 2021. http://dx.doi.org/10.29289/259453942021v31s2072.

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Introduction: Breast cancer is one of the neoplasms that most cause death in women. Among these, there are some subtypes of greater biological aggressiveness, such as triple negative and HER overexpressed, which are associated with greater recurrence and mortality. Adenoid cystic carcinoma (ACC), salivary gland type, represents less than 0.1% of primary breast carcinomas and has indolent biological behavior and favorable prognosis compared with nonspecial triplenegative types. Case Report: A 51-year-old woman diagnosed with locally advanced ACC in the right breast, with negative immunohistoche

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Zerwes, Felipe Pereira, Ruffo de Freitas Junior, Vilmar Marques de Oliveira, et al. "SYSTEMIC TREATMENT FOR EARLY-STAGE TRIPLE-NEGATIVE BREAST CANCER: A RECOMMENDATION FROM AN EXPERT PANEL OF THE BRAZILIAN SOCIETY OF MASTOLOGY." In Brazilian Breast Cancer Symposium 2022. Mastology, 2022. http://dx.doi.org/10.29289/259453942022v32s2060.

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Objective: The aim of this study was to assess the knowledge and attitudes of members of the Brazilian Society of Mastology (SBM) about the systemic treatment of triple-negative breast cancer (TNBC). Methods: All 1,400 SBM members were invited to answer a survey with 44 objective questions. An expert meeting was held in December 2021, with the participation of 27 experts and 3 ad hoc consultants. Panelists responded to the survey before and after the meeting (brainstorm). Responses that reached 70% agreement were considered consensual. Results: There was consensus regarding the indications of

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Soares, Leonardo Ribeiro, Vilmar Marques de Oliveira, Antonio Luiz Frasson, et al. "LOCOREGIONAL TREATMENT FOR EARLY-STAGE TRIPLE-NEGATIVE BREAST CANCER: A RECOMMENDATION FROM AN EXPERT PANEL OF THE BRAZILIAN SOCIETY OF MASTOLOGY." In Brazilian Breast Cancer Symposium 2022. Mastology, 2022. http://dx.doi.org/10.29289/259453942022v32s2065.

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Objective: The aim of this study was to evaluate the knowledge and attitudes of the members of the Brazilian Society of Mastology (SBM) about the locoregional treatment of triple-negative breast cancer (TNBC). Methods: All 1,400 SBM members were invited to answer a survey of 44 objective questions. An expert meeting was held in December 2021, with the participation of 27 experts and 3 ad hoc consultants. Panelists responded to the survey before and after the meeting (brainstorm). Responses that reached 70% agreement were considered consensual. Results: In a patient undergoing conservative surg

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Lafont, J., J. H. Catherine, M. Lejeune, U. Ordioni, R. Lan, and F. Campana. "Manifestations buccales de la sclérose tubéreuse de Bourneville." In 66ème Congrès de la SFCO. EDP Sciences, 2020. http://dx.doi.org/10.1051/sfco/20206603014.

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L’objectif de ce travail est de faire le point sur les manifestations buccales de la sclérose tubéreuse de Bourneville (STB) à travers le cas d’un jeune patient. Un jeune homme de 15 ans était adressée pour la mise en place de minivis orthodontique afin de fermer des espaces d’agénésies de 35 et 45. L’interrogatoire retrouvait une STB dont les manifestations épileptiques étaient traitées par de la lamotrigine 75mg/j et de la carbamazépine LP 200mg/j. L’examen clinique exo-buccal retrouvait des macules hypochromiques sur le membre inférieur droit, des angiofibromes faciaux et une malformation v

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Wang, Jiashi, Kevin Lai, Madelyn Light, et al. "Abstract 418: Highly efficient duplex DNA tagging strategy improves accuracy of detecting ultra-low-frequency mutations through consensus read reconstruction." In Proceedings: AACR Annual Meeting 2018; April 14-18, 2018; Chicago, IL. American Association for Cancer Research, 2018. http://dx.doi.org/10.1158/1538-7445.am2018-418.

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Bailey, Matthew H., Liang-Bo Wang, Wen-Wei Liang, et al. "Abstract 419: Reproducibility assessment of mutations calls in exome- and whole-genome sequencing using consensus calling from TCGA and ICGC." In Proceedings: AACR Annual Meeting 2018; April 14-18, 2018; Chicago, IL. American Association for Cancer Research, 2018. http://dx.doi.org/10.1158/1538-7445.am2018-419.

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Assis, Amilcar Alves, Mauro Passos, Rodrigo Kouzak, Karoline Evangelista, and Natasha Caldas. "BREAST CANCER IN YOUNG PATIENTS: PROGNOSTIC AND PROFILE EPIDEMIOLOGICAL ANALYSIS IN A TERTIARY HOSPITAL." In Abstracts from the Brazilian Breast Cancer Symposium - BBCS 2021. Mastology, 2021. http://dx.doi.org/10.29289/259453942021v31s2093.

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Breast cancer is the second most prevalent and first in mortality in Brazilian women. Its incidence has increased in recent years in all age groups. According to the Instituto Nacional do Câncer in 2019, 59,700 new cases of breast cancer are expected, with an estimated risk of 56.33 cases per 100 women. The diagnosis of breast cancer is more frequent in women after 50 years of age; it is estimated that only 25% of all cases occur in women below the age of 50 years; however, there was a literature consensus that tumors in this young age group have a worse prognosis, both because they are biolog

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Suchkov, Sergey. "Strategies for integrating Personalized and Precision Medicine (PPM) into Reproductive Healthcare Practice to Secure the Human Healthcare, Wellness and Biosafety: Forging the Grand Consensus." In World Conference on Gynecology, Obstetrics, and Pediatrics. Eurasia Conferences, 2025. https://doi.org/10.62422/978-81-981865-0-8-002.

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A new systems approach to diseased states and wellness result in a new branch in the healthcare services, namely, personalized and precision medicine (PPM). Meanwhile, the era of genomics-based medicine and thus genomics biomarkers promises to provide molecular tests that will permit PPM as applicable to personalized and precision oncology (PPO). Using the PCL-5 questionnaire and according to the DSM-5 criteria for PTSD, 20% were To achieve the implementation of PPM-guided oncology concept, it is necessary to create a funda-mentally new strategy based upon the subclinical recognition of biopre

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