Cargando…

Ultrasensitive analysis of genetic instability related to chemical exposure

Our concerns have been raised about whether prolonged exposure to ammunition-related chemicals could correlate with genomic instability predisposing to lung carcinogenesis. The group of professional soldiers engaged in routine ammunition analysis and its explosive properties testing. To assess the p...

Descripción completa

Detalles Bibliográficos
Autores principales:	Domoradzki, Tomasz, Grochowski, Piotr, Jaśkiewicz, Anna, Pająk, Beata
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Springer Berlin Heidelberg 2021
Materias:	Human Genetics • Original Paper
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8979864/ https://www.ncbi.nlm.nih.gov/pubmed/34967917 http://dx.doi.org/10.1007/s13353-021-00677-6

Ejemplares similares

Targeting the JAK2/STAT3 Pathway—Can We Compare It to the Two Faces of the God Janus?
por: Jaśkiewicz, Anna, et al.
Publicado: (2020)

WP1234—A Novel Anticancer Agent with Bifunctional Activity in a Glioblastoma Model
por: Pająk, Beata, et al.
Publicado: (2022)

Synergistic Anticancer Effect of Glycolysis and Histone Deacetylases Inhibitors in a Glioblastoma Model
por: Pająk, Beata, et al.
Publicado: (2021)

Genetics and epigenetics of autism spectrum disorder—current evidence in the field
por: Wiśniowiecka-Kowalnik, Barbara, et al.
Publicado: (2019)

Genomic instability in the PARK2 locus is associated with Parkinson’s disease
por: Ambroziak, Wojciech, et al.
Publicado: (2015)

Estimating genomic instability mediated by Alu retroelements in breast cancer
por: Fazza, Ana Cristina, et al.
Publicado: (2009)

Population-genetic study of Balkan endemic nephropathy in Serbia
por: Marinkovic, D., et al.
Publicado: (2007)

Nuclear genes involved in mitochondrial diseases caused by instability of mitochondrial DNA
por: Rusecka, Joanna, et al.
Publicado: (2018)

Differential expression of lung adenocarcinoma transcriptome with signature of tobacco exposure
por: Hammouz, Raneem Y., et al.
Publicado: (2020)

Genetic diversity in Kashubs: the regional increase in the frequency of several disease-causing variants
por: Jankowski, Maciej, et al.
Publicado: (2022)

Minimal prevalence of Huntington’s disease in the South of Brazil and instability of the expanded CAG tract during intergenerational transmissions
por: de Castilhos, Raphael Machado, et al.
Publicado: (2019)

Association study of folate-related enzymes (MTHFR, MTR, MTRR) genetic variants with non-obstructive male infertility in a Polish population
por: Kurzawski, Mateusz, et al.
Publicado: (2015)

Intracardiac tumor as a rare manifestation of genetic syndromes—presentation of a family with Gorlin syndrome and a literature review
por: Szczałuba, Krzysztof, et al.
Publicado: (2020)

Individual Differences in Relative Telomere Length in Mentally Healthy Subjects: The Effect of TERT Gene Polymorphism and Urban Residency
por: Kazantseva, A. V., et al.
Publicado: (2022)

Smoking and caffeine consumption: a genetic analysis of their association
por: Treur, Jorien L., et al.
Publicado: (2016)

The genetics of aniridia — simple things become complicated
por: Wawrocka, Anna, et al.
Publicado: (2018)

Mutational analysis in podocin-associated hereditary nephrotic syndrome in Polish patients: founder effect in the Kashubian population
por: Lipska, Beata S., et al.
Publicado: (2013)

Human population genetic structure detected by pain-related mu opioid receptor gene polymorphisms
por: López Soto, Eduardo Javier, et al.
Publicado: (2015)

Genetic frequencies related to severe or profound sensorineural hearing loss in Inner Mongolia Autonomous Region
por: Liu, Yongzhi, et al.
Publicado: (2016)

Spontaneous chromosomal instability in peripheral blood lymphocytes from two molecularly confirmed Italian patients with Hereditary Fibrosis Poikiloderma: insights into cancer predisposition
por: Roversi, Gaia, et al.
Publicado: (2021)

Current genetic methodologies in the identification of disaster victims and in forensic analysis
por: Ziętkiewicz, Ewa, et al.
Publicado: (2011)

Cancer-related worry and risk perception in Brazilian individuals seeking genetic counseling for hereditary breast cancer
por: Palmero, Edenir Inêz, et al.
Publicado: (2020)

Splicing mutations in human genetic disorders: examples, detection, and confirmation
por: Anna, Abramowicz, et al.
Publicado: (2018)

Analysis of 31 STR loci in the genetic isolate of Carloforte (Sardinia, Italy)
por: Robledo, Renato, et al.
Publicado: (2009)

RNA‐Seq Analysis of Genetic and Transcriptome Network Effects of Dual‐Trait Selection for Ethanol Preference and Withdrawal Using SOT and NOT Genetic Models
por: Kozell, Laura B., et al.
Publicado: (2020)

Common BMI and diabetes-related genetic variants: A pilot study among indigenous people in the Brazilian Amazon
por: Diniz, Isabela Guerreiro, et al.
Publicado: (2022)

Missense mutations and polymorphisms of the MC4R gene in Polish obese children and adolescents in relation to the relative body mass index
por: Nowacka-Woszuk, Joanna, et al.
Publicado: (2011)

The Many Faces of Rap1 GTPase
por: Jaśkiewicz, Anna, et al.
Publicado: (2018)

Split-hand/foot malformation - molecular cause and implications in genetic counseling
por: Sowińska-Seidler, Anna, et al.
Publicado: (2013)

AP4B1-associated hereditary spastic paraplegia: expansion of phenotypic spectrum related to homozygous p.Thr387fs variant
por: Szczałuba, Krzysztof, et al.
Publicado: (2020)

Population analysis of vitamin D receptor polymorphisms and the role of genetic ancestry in an admixed population
por: Lins, Tulio C., et al.
Publicado: (2011)

Genetic instability-related lncRNAs predict prognosis and influence the immune microenvironment in breast cancer
por: Lv, Zhenyi, et al.
Publicado: (2022)

Clinical interpretation of copy number variants in the human genome
por: Nowakowska, Beata
Publicado: (2017)

Analysis of apolipoprotein E genetic polymorphism in a large ethnic Hakka population in southern China
por: Zhong, Zhixiong, et al.
Publicado: (2018)

Privacy and confidentiality measures in genetic testing and counselling: arguing on genetic exceptionalism again?
por: Witt, Magdalena M., et al.
Publicado: (2016)

Occupational exposure of workers to pesticides: Toxicogenetics and susceptibility gene polymorphisms
por: Adad, Lúcia Maria de Miranda, et al.
Publicado: (2015)

No dynamic changes in the expression of genes related to the epigenetic mechanism during acute exercise
por: Światowy, Witold Józef, et al.
Publicado: (2022)

Single nucleotide polymorphism rs11614913 associated with CC genotype in miR-196a2 is overrepresented in laryngeal squamous cell carcinoma, but not salivary gland tumors in Polish population
por: Skalski, Marcin, et al.
Publicado: (2018)

Application of array comparative genomic hybridization in 256 patients with developmental delay or intellectual disability
por: Bartnik, Magdalena, et al.
Publicado: (2013)

Biochemical and genetic analysis of butyrylcholinesterase (BChE) in a family, due to prolonged neuromuscular blockade after the use of succinylcholine
por: Garcia, Daniel Fantozzi, et al.
Publicado: (2011)

Cannot write session to /tmp/vufind_sessions/sess_m26kij1svksjdmakg83tfnfnim