Results 211 to 220 of about 611,533 (294)

A fixation-weighted null model for the proportion of sex chromosome-autosome fusions. [PDF]

MicroPubl Biol
Schmalz S, Blackmon H.
europepmc   +1 more source

Dynamics of Size and Shape Variation During Embryonic Development in the Balkan Crested Newt

Journal of Experimental Zoology Part B: Molecular and Developmental Evolution, EarlyView.
Morphological variance in Triturus ivanbureschi embryos fluctuates during the tailbud phase, coinciding with developmental arrest caused by the balanced lethal system. Prehatching embryos show uniform variance. Our study reveals dynamics of morphological variability during early development and provides a baseline for further studies.
Marko Bugarčić, Ana Ivanović, Milena Cvijanović, Maja Ajduković, Marija Drobnjaković, Ben Wielstra, Tijana Vučić   +6 more
wiley   +1 more source

Newly unveiled meiosis elucidates the unreduced gamete frequency and its impact on the evolution of the Lemna minor complex. [PDF]

J Exp Bot
Lee 이유리 Y, Schubert V, Stepanenko A, Kim G, Braglia L, Schubert I, Morello L.   +6 more
europepmc   +1 more source

The FOXQ1/SSBP2 Regulatory Axis Drives Malignant Progression of Melanoma

Molecular Carcinogenesis, EarlyView.
ABSTRACT Melanoma is a highly aggressive skin cancer with poor prognosis, often linked to excessive UV exposure. Despite advancements in immunotherapy and targeted treatments, melanoma's invasiveness and metastatic potential remain significant challenges.
Xiaoyu Zhang, Yu Hou, Jiahui Liu, Yuehua Han, Jiangang Feng   +4 more
wiley   +1 more source

Markerless gene deletion in <i>Porphyromonas gingivalis</i> using a <i>pheS*</i>-based counterselection system. [PDF]

Microbiol Spectr
Kim H-M, Davey ME, Yu M.
europepmc   +1 more source

Phenotypic Exploration in Patients with Heterozygous Variant in AFG3L2 Gene: A Case‐Series and Literature Review

Movement Disorders Clinical Practice, EarlyView.
Abstract Background Variants in AFG3‐Like Matrix AAA Peptidase, Subunit 2 (AFG3L2) gene are associated with diverse clinical phenotypes. Here, we describe phenotypic findings of two unrelated children with de novo heterozygous variant and one family with inherited heterozygous variant in AFG3L2 gene.
Sangeetha Yoganathan, Laura Tochen, Jacky Ganguly, Sayoni Roy Chowdhury, Haya S AlFaris, Vivek Pai, Andrea LeBlanc‐Millar, Sara Breitbart, Hrishikesh Kumar, Manohar Shroff, Arun Reginald, Grace Yoon, Alfonso Fasano, George M Ibrahim, Carolina Gorodetsky   +14 more
wiley   +1 more source

LINE-1 insertion intermediates recombine with one another or with DNA breaks to form genome rearrangements. [PDF]

Nat Commun
Mendez-Dorantes C, Kalinowski JC, Burn A, Schofield P, Law CT, Isik E, Burns KH.   +6 more
europepmc   +1 more source

Meiotic cohesin-based chromosome structure is essential for homologous chromosome pairing in Schizosaccharomyces pombe. [PDF]

Chromosoma, 2016
Ding DQ, Matsuda A, Okamasa K, Nagahama Y, Haraguchi T, Hiraoka Y.   +5 more
europepmc   +1 more source

Resolving Complex Structural Variants in Undiagnosed Rare Movement Disorders via Multimodal Genomics and Multi‐omics

Movement Disorders, EarlyView.
Abstract Background Long‐read sequencing and multi‐omic analytical frameworks are increasingly being adopted in rare disease diagnostics. However, clinical workflows comprehensively integrating these methodologies remain uncommon. Objective This study aimed to assess the potential and limitations of integrating long‐read genomic, transcriptomic, and ...
Ugo Sorrentino, Melanie Brugger, Alice Saparov, Ivana Dzinovic, Philip Harrer, Sandy Lösecke, Kevork Derderian, Martin Pavlov, Robert Kopajtich, Holger Prokisch, Arcangela Iuso, Maria Mazurkiewicz‐Bełdzińska, Deike Weiss, Christina Ludwig, Miriam Abele, Julia Mergner, Juliane Winkelmann, Theresa Brunet, Michał Schinwelski, Elisabeth Graf, Katja Kloth‐Stachnau, Theresia Herget, Magdalena Krygier, Michael Zech   +23 more
wiley   +1 more source

Polymorphism can extensively reshape the genome-wide crossover landscape in Arabidopsis thaliana. [PDF]

Nat Commun
Madec B, Sémery M, Lian Q, Yassine M, Léonard-Moniot L, Espagne É, Piquerez S, Girard C.   +7 more
europepmc   +1 more source