Results 61 to 70 of about 149 (122)

Reconstructing the Past and the Present: The Ethnographic Films Made by the Estonian National Museum (1961–1989)

Journal of Ethnology and Folkloristics, 2011
This article analyses the films made by the Estonian National Museum in the 1970s and the 1980s both from the point of view of the filming activity and of the content of these films.
Liivo Niglas, Eva Toulouze
doaj  

Advanced Molecular Analysis in Hemophilia A in a Single Step: Next Generation Sequencing (NGS) and Copy Number Variation (CNV) Analysis

International Journal of Laboratory Hematology, EarlyView.
ABSTRACT Background Hemophilia A, an X‐linked bleeding disorder caused by pathogenic variants in the F8 gene, requires precise genetic diagnosis for optimal management. Conventional stepwise sequence and copy number variation (CNV) analyses are time‐consuming and may leave some cases unresolved.
Enise Avci Durmusalioglu, Esra Isik, Basak Durmus Ozen, Mehmet Mert Topaloglu, Nihal Karadas, Kaan Kavakli, Melike Sezgin Evim, Tolga Aslan, Erşen Kavak, Adalet Meral Gunes, Funda Tayfun Kupesiz, Alphan Kupesiz, Fahri Sahin, Tahir Atik   +13 more
wiley   +1 more source

Competitive exclusion, not predation, likely drove the decline in native fish diversity following carnivorous fish introductions to Lake Titicaca in the mid‐20th century

Journal of Fish Biology, EarlyView.
Abstract Lake Titicaca is a continental centre for ichthyological biodiversity, with over 90% of native species being endemic. However, these species face significant threats from invasive species, particularly from invasive salmonids and invasive Argentine pejerrey.
Daniel A. Villar, Renzo Turpo Aroquipa, Cesar Gamarra Peralta, Edmundo Moreno Terrazas   +3 more
wiley   +1 more source

Ethno-linguistic situation in the forest zone of eastern europe in the first centuries ad and the data of jordanes’ getica

, 2020
© 2018, Ural University Press. All rights reserved. The comparative analysis of folk-names lists from the Jordanes’ Getica 116 (“Hermanaric’s arctoi gentes” in author’s reconstruction, information comes from the middle 4th century AD) and early Russian ...

core  

Digital twins and the virtual epileptic patient: Toward simulation‐based neurology

Epilepsia, EarlyView.
Antonella Riva, Francesca Spataro, Antonio Cerasa, Pasquale Striano, Egidio D'Angelo   +4 more
wiley   +1 more source

Evaluation of Mutation Risk Using Patient‐Derived Organoids in Patients With Lynch Syndrome

International Journal of Cancer, Volume 159, Issue 10, Page 2585-2594, 15 November 2026.
ABSTRACT Lynch syndrome (LS) is a hereditary cancer predisposition syndrome caused by germline mutation of DNA mismatch repair (MMR) genes, most notably associated with colorectal cancer. Although LS patients face high risk of CRC, risk can vary even among those with the same pathogenic MMR germline mutations. We suggest a functional assay platform for
Youmi Shin, Dong Keon Kim, Yoojeong Seo, Hyeon Hee Lee, Jihye Park, Soo Jung Park, Jae Jun Park, Jae Hee Cheon, Jongwon Oh, Sanghoo Lee, Tae Il Kim   +10 more
wiley   +1 more source

Cyrillic in the Geolinguistic Space. [PDF]

Her Russ Acad Sci, 2022
Aref'ev AL.
europepmc   +1 more source

Genome Sequencing Outperforms Exome Sequencing in Formalin‐Fixed Paraffin Embedded Tumors Leading to Improved Treatment Options

Cancer Medicine, Volume 15, Issue 11, November 2026.
ABSTRACT Precision oncology is based on comprehensive molecular characterization of a patient's tumor. This is mostly realized by next‐generation sequencing panels or exome sequencing. Data on the value of genome sequencing from formalin‐fixed paraffin embedded (FFPE) material in a clinical setting is still scarce.
Nadja Ballin, Alexander Ott, Michaela Pogoda, Florian Harmuth, Vijay Kumar Ulaganathan, Anton Karelin, Cristiana Roggia, Irina Bonzheim, Stephan Singer, Holly Sundberg‐Malek, Pavlos Missios, Stephan Ossowski, Tobias B. Haack, Olaf Riess, Michael Bitzer, Nisar Malek, Christopher Schroeder, Sorin Armeanu‐Ebinger   +17 more
wiley   +1 more source

Genetic Polymorphisms of Cytochromes P450 in Finno-Permic Populations of Russia. [PDF]

Genes (Basel), 2022
Dzhaubermezov M, Ekomasova N, Mustafin R, Gabidullina L, Galimova Y, Nurgalieva A, Valova Y, Prokofyeva D, Khusnutdinova E.   +8 more
europepmc   +1 more source

Clinical Functional Assignment of TPMT and NUDT15 Alleles by the Clinical Pharmacogenetics Implementation Consortium Pharmacogene Curation Expert Panel

Clinical Pharmacology &Therapeutics, Volume 120, Issue 5, Page 1427-1437, November 2026.
The Clinical Pharmacogenetics Implementation Consortium (CPIC) TPMT/NUDT15 Pharmacogene Curation Expert Panel (PCEP) conducted a comprehensive review of clinical, laboratory, and computational evidence to determine the clinical function assignments for TPMT and NUDT15 star alleles.
Bailey M. Tibben, Maud Maillard, Victoria M. Pratt, Ann M. Moyer, Debbie M. Figueroa, Michelle Whirl‐Carrillo, Andrea Gaedigk, Gabriele Stocco, Matthias Schwab, Kelly E. Caudle, Jun J. Yang   +10 more
wiley   +1 more source