Results 161 to 170 of about 59,040 (314)

Development of a High‐Resolution MNP Marker System for Aquatic Biodiversity Monitoring: A Case Study With Schizothorax prenanti in the Yangtze River

Molecular Ecology Resources, Volume 26, Issue 1, January 2026.
ABSTRACT Effective monitoring of aquatic biodiversity is critical for conservation, yet current approaches such as mitochondrial COI barcoding and microsatellite markers exhibit limitations in resolution, sensitivity, and scalability, particularly for detecting low‐abundance or degraded DNA in mixed aquatic samples.
Baolong Zhang, Wei Jiang, Zhiwei Fang, Hao Chen, Nan Jiang, Junfei Zhou, Renjing Wan, Sha Li, Tiantian Li, Lu Cai, Huiyin Song, Lun Li, Lifen Gao, Lihong Chen, Hai Peng   +14 more
wiley   +1 more source

Used version of WhatsHap for "Haplotype Threading: Accurate Polyploid Phasing from Long Reads"

, 2020
Sven Schrinner, Rebecca Serra Mari, Jana Ebler, Tobias Marschall, Gunnar W. Klau   +4 more
openalex   +1 more source

Phylogenetic patterns and polyploid evolution within the Mediterranean genusCentaurium(Gentianaceae ‐ Chironieae) [PDF]

, 2005
Guilhem Mansion, Louis Zeltner, François Bretagnolle   +2 more
openalex   +1 more source

Mitochondrial DNA Variation in the Aging Human Cerebral Cortex and Cerebellum

Aging Cell, Volume 25, Issue 1, January 2026.
We used cerebellum and frontal cortex whole genome sequencing data from the North American Brain Expression Consortium to investigate mitochondrial DNA deletions, single nucleotide variants, and copy number. We found significant differences between brain regions and age effects for all these metrics, which illustrate mitochondrial changes in healthy ...
Audrey A. Omidsalar, David R. Tyrpak, J. Andrew MacKay, Kelvin Yen, Pinchas Cohen, Geidy Serrano, Thomas G. Beach, Michael A. Nalls, Dena G. Hernandez, Mark R. Cookson, Andrew B. Singleton, J. Raphael Gibbs, North American Brain Expression Consortium, Brooke E. Hjelm   +13 more
wiley   +1 more source

Trait Mapping Utilizing a Newly Constructed Genome for Allohexaploid Invasive Eurasian Watermilfoil (Myriophyllum spicatum) Reveals a Non‐Target Site QTL Associated With Fluridone Resistance

Evolutionary Applications, Volume 19, Issue 1, January 2026.
ABSTRACT Herbicides are a valuable tool in agricultural ecosystems to manage nuisance species. Due to the reliance on herbicides for weed control, herbicide resistance is a growing concern. Herbicides are also used extensively in aquatic and natural systems, but the genetics and evolutionary dynamics of resistance are not as frequently incorporated ...
Del Hannay, Gregory M. Chorak, Alex Harkess, Josh Clevenger, Josh T. Cuperus, Haley Hale, Laramie Aközbek, Zachary Meharg, Sarah B. Carey, Zachary Myers, Christine Queitsch, Arianna Stamatoyannopoulos, Ryan A. Thum   +12 more
wiley   +1 more source

Polyploidization delay in rat hepatocytes under liver growth inhibition by hypokinesia [PDF]

A study of young rats, weighing 55 to 59 g, after being for 10 days in conditions of limited mobility, shows a retardation of body growth as well as that of liver growth.
Brodskiy, V. Y., Faktor, V. M., Li, S. Y., Malyutin, V. F.   +3 more
core   +1 more source

Studia embriologiczne nad poliploidalnymi formami Trifolium repens L. [Embryological studies on polyploid forms of Trifolium repens]

, 2015
K. Bijok, M. Górol, S. Góral
openalex   +2 more sources

Development of iFOX‐hunting as a functional genomic tool and demonstration of its use to identify early senescence‐related genes in the polyploid Brassica napus [PDF]

, 2017
Juan Ling, Renjie Li, Chinedu Charles Nwafor, Junluo Cheng, Maoteng Li, Qing Xu, Jian Wu, Lu Gan, Qingyong Yang, Chao Liu, Ming Chen, Yongming Zhou, Edgar B. Cahoon, Chunyu Zhang   +13 more
openalex   +1 more source

Additional file 4 of PolyHaplotyper: haplotyping in polyploids based on bi-allelic marker dosage data

, 2022
Roeland E. Voorrips, Giorgio Tumino
openalex   +1 more source

ITGA2B/ITGB3‐Related Macrothrombocytopenia Associated With Gain‐of‐Function Mutations in ITGA2B or ITGB3 Genes

Journal of Cellular and Molecular Medicine, Volume 30, Issue 1, January 2026.
ABSTRACT Glanzmann thrombasthenia (GT) is an inherited hemorrhagic disorder characterised by impaired platelet functions, manifested clinically as spontaneous bleeding. It is usually inherited in an autosomal recessive manner. Platelet dysfunction in patients with GT is caused by quantitative and/or qualitative deficiencies in αIIbβ3, which result from
Jiao Wu, Han Yan, Zijian Li, Yilin Zhu, Ruonan Shao, Honglei Xin, Tongyu Jia, Mengyu Ge, Lu Zhang, Suyu Jiang, Jianhua Mao, Jiansong Huang, Chao Fang, Xiaodong Xi, Xiaofeng Shi   +14 more
wiley   +1 more source