Categoría: Articulos
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Study finds hidden mutation rates may shape cancer risk
A new study by scientists at City of Hope and TGen, part of City of Hope, found surprisingly large differences in the number of mutations present in the organs of healthy individuals. Some study participants had mutation counts similar to those typical…
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The new article is now available. Intractable & Rare Diseases Research
[ Advance Publication ] [ Title ] Subclinical ascitic neutrophilia is associated with short-term mortality in cirrhosis [ Author ] Alp Serhat Kahveci,Melis Celdir,Tomohiro Tanaka [ Advance Pub. date ] 2026-10-02 [ DOI ] https://doi.org/10.5582/irdr.20…
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The new article is now available. Intractable & Rare Diseases Research
[ Advance Publication ] [ Title ] Subclinical ascitic neutrophilia is associated with short-term mortality in cirrhosis [ Author ] Alp Serhat Kahveci,Melis Celdir,Tomohiro Tanaka [ Advance Pub. date ] 2026-10-02 [ DOI ] https://doi.org/10.5582/irdr.20…
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How damaged mitochondria may contribute to liver disease
Mitochondria supply cells with energy, and they also play an important role in metabolism. The Institute of Biochemistry and Molecular Biology I at Heinrich Heine University Düsseldorf (HHU) and University Hospital Düsseldorf (UKD) are researching the …
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Children with a common genetic variant may have more inflammation in response to an asthma drug
Children with a variant in the SERPINE1 gene—which is found in 60% of the population—may be less responsive to mepolizumab, a drug used to treat asthma flares, according to a study published in the Journal of Allergy and Clinical Immunology.
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Children with a common genetic variant may have more inflammation in response to an asthma drug
Children with a variant in the SERPINE1 gene—which is found in 60% of the population—may be less responsive to mepolizumab, a drug used to treat asthma flares, according to a study published in the Journal of Allergy and Clinical Immunology.
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Insertion or deletion variants in <i>TAF15</i> exon 15 are genetic factors impacting the prognosis of amyotrophic lateral sclerosis in a Japanese cohort
European Journal of Human Genetics, Published online: 01 October 2026; doi:10.1038/s41431-026-02249-wInsertion or deletion variants in TAF15 exon 15 are genetic factors impacting the prognosis of amyotrophic lateral sclerosis in a Japa…
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Burden of pathogenic variants in genes associated with medically actionable disease in the Slovenian population
IntroductionThe prevalence of pathogenic variants in disease-related genes is population-specific and is of vital importance for the development of national health policies. It is especially important with medically actionable diseases, where early int…