Saved in:
| Main Authors: | Keith, Nathan, Glaholt, Stephen P, Jackson, Craig E, Young, Kim, De Schamphelaere, Karel, Colbourne, John K, Shaw, Joseph R |
|---|---|
| Format: | Artículo científico |
| Language: | en |
| Published: |
Molecular ecology
2026
|
| Subjects: | |
| Online Access: | https://pubmed.ncbi.nlm.nih.gov/42041136/ |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
A transient mutational burst occurs during yeast colony development.
by: Agier, Nicolas, et al.
Published: (2025)
by: Agier, Nicolas, et al.
Published: (2025)
Functional roles of mastigonemes in Ectocarpus gamete swimming revealed by CRISPR-Cas9 mutagenesis.
by: Harada, Minori, et al.
Published: (2026)
by: Harada, Minori, et al.
Published: (2026)
Mutational features of chromids and chromosomes in provide new insights into the evolution of secondary replicons.
by: Jiang, Wanyue, et al.
Published: (2025)
by: Jiang, Wanyue, et al.
Published: (2025)
The negligible mutagenic effects of norfloxacin on the genome of the fission yeast ATCC-16979.
by: Lin, Tongtong, et al.
Published: (2025)
by: Lin, Tongtong, et al.
Published: (2025)
Determination of leachate toxicity through acute toxicity using Daphnia pulex and anaerobic toxicity assays
by: Y. S. Carabalí-Rivera
Published: (2017)
by: Y. S. Carabalí-Rivera
Published: (2017)
Cadmium sub-lethal effects on Daphnia magna - A new take on an old subject.
by: Pinto, Albano, et al.
Published: (2025)
by: Pinto, Albano, et al.
Published: (2025)
Daphnia pulex through physical and chemical factors
by: Haghparast, S., et al.
Published: (2011)
by: Haghparast, S., et al.
Published: (2011)
Identification of a Germline XAF1 Mutation in Patients With Gastrointestinal Cancers
by: Guan-Xin Xu, et al.
Published: (2026)
by: Guan-Xin Xu, et al.
Published: (2026)
A Novel Germline MUTYH Mutation (p.W156∗) in High‐Grade Astrocytoma, IDH Mutant
by: Lulu Zhang, et al.
Published: (2025)
by: Lulu Zhang, et al.
Published: (2025)
CAVaLRi: An Algorithm for Rapid Identification of Diagnostic Germline Variation
by: Robert J. Schuetz, et al.
Published: (2024)
by: Robert J. Schuetz, et al.
Published: (2024)
Tissue specific per base pair resolution exome and genome mutation susceptibilities
by: Schmalohr, Corinna, et al.
Published: (2025)
by: Schmalohr, Corinna, et al.
Published: (2025)
Can bystander effects of metals in Daphnia magna be mediated by DNA methylation?
by: Jeremias, Guilherme, et al.
Published: (2025)
by: Jeremias, Guilherme, et al.
Published: (2025)
Mutation Spectrum of Hemoglobinopathies in Tunisia
by: Imen Moumni, et al.
Published: (2026)
by: Imen Moumni, et al.
Published: (2026)
DEGRADACIÓN HIDROLÍTICA DE CLORPIRIFOS Y EVALUACIÓN DE LA TOXICIDAD DEL EXTRACTO HIDROLIZADO CON Daphnia pulex
by: Jhon Fredy Narváez Valderrama
Published: (2014)
by: Jhon Fredy Narváez Valderrama
Published: (2014)
Discovering genotype-phenotype relationships with machine learning and the Visual Physiology Opsin Database (VPOD).
by: Frazer, Seth A, et al.
Published: (2024)
by: Frazer, Seth A, et al.
Published: (2024)
Genotype/Phenotype Relationship: Lessons From 137 Patients With PMM2‐CDG
by: Sander Pajusalu, et al.
Published: (2024)
by: Sander Pajusalu, et al.
Published: (2024)
Expanding the Genotypic Landscape of Congenital Stationary Night Blindness in an Ethnically Diverse Canadian Population
by: Jennifer Ling, et al.
Published: (2026)
by: Jennifer Ling, et al.
Published: (2026)
Factors influencing the start of development in Daphnia pulex winter eggs [Translation from: Biological Reviews Vol. 13, 24-26, 1951]
by: Ogi, K., et al.
Published: (1951)
by: Ogi, K., et al.
Published: (1951)
ALPL Mutations With Dominant‐Negative Effect in Infantile Hypophosphatasia Monozygotic Twins
by: Luna Hao, et al.
Published: (2026)
by: Luna Hao, et al.
Published: (2026)
Phenotypic Characterization of ALS‐Causing SOD1 Mutations Affecting Polypeptide Length
by: Mariusz Berdyński, et al.
Published: (2025)
by: Mariusz Berdyński, et al.
Published: (2025)
Polycystic Ovary Syndrome May Be Associated With a Novel Mitochondrial tRNAAsp Mutation
by: Yu Ding, et al.
Published: (2025)
by: Yu Ding, et al.
Published: (2025)
Clinically Translatable Mutation‐Based Biomarkers in Ascending Aortic Aneurysm: A Bibliometric Study
by: Fan Yang, et al.
Published: (2026)
by: Fan Yang, et al.
Published: (2026)
A Comprehensive Review of Gene Mutations in Inherited Blood Disorders Among the Saudi Population
by: Nancy S. Younis, et al.
Published: (2026)
by: Nancy S. Younis, et al.
Published: (2026)
Dilated Cardiomyopathy May Be Associated With a Novel Mitochondrial tRNASer(AGY) Mutation
by: Yu Ding, et al.
Published: (2025)
by: Yu Ding, et al.
Published: (2025)
Deciphering the Mutational Background in Citrin Deficiency Through a Nationwide Study in Japan and Literature Review
by: Jun Kido, et al.
Published: (2025)
by: Jun Kido, et al.
Published: (2025)
Cellular Functional Analyses of ARX Variants Reveal New Insights Into Genotype–Phenotype Correlations in Neurodevelopmental Disorders Among Male and Female Patients
by: Rasha Faraj, et al.
Published: (2026)
by: Rasha Faraj, et al.
Published: (2026)
Distinct Pathogenic Mechanisms of Two Novel NHS Mutations Identified in Chinese Han Families With Nance–Horan Syndrome
by: Li Li, et al.
Published: (2026)
by: Li Li, et al.
Published: (2026)
Biallelic Recessive Mutations in TLE6 and NLRP5 Cause Female Infertility Characterized by Human Early Embryonic Arrest
by: Ruiqi Li, et al.
Published: (2024)
by: Ruiqi Li, et al.
Published: (2024)
In silico Analysis of CHD4 Mutations Reveals Domain‐Specific Impacts on Cardiovascular Disorders Among Patients With Rare Diseases
by: Apolonia Novillo, et al.
Published: (2026)
by: Apolonia Novillo, et al.
Published: (2026)
Simultaneous Genotyping of Three Nonsynonymous SNVs, rs1042602, rs1426654, and rs16891982 Involved in Skin Pigmentation by Fluorescent Probe‐Based Melting Curve Analysis
by: Mikiko Soejima, et al.
Published: (2025)
by: Mikiko Soejima, et al.
Published: (2025)
Reclassification of VUS Using ACMG/AMP Criteria Adapted for Sarcomeric Genes Related to Hypertrophic Cardiomyopathy: Resolution Rate and Considerations
by: Silvia Caroselli, et al.
Published: (2025)
by: Silvia Caroselli, et al.
Published: (2025)
A Tertiary Lymphoid Structure–Derived Prognostic Signature Integrates Immune Microenvironment and Mutational Landscapes in Clear Cell Renal Cell Carcinoma
by: Xuanyu Zhou, et al.
Published: (2026)
by: Xuanyu Zhou, et al.
Published: (2026)
Clinical and Genetic Characteristics of Two Cases With Developmental and Epileptic Encephalopathy 93 Caused by Novel ATP6V1A Mutations and Literature Review
by: Jian Ma, et al.
Published: (2024)
by: Jian Ma, et al.
Published: (2024)
Clinic Examination and Gene Diagnosis for a Birt–Hogg–Dubé Syndrome Family With a Novel flcn Frameshift Mutation Causing Nonsense‐Mediated mRNA Degradation
by: Yang Xu, et al.
Published: (2025)
by: Yang Xu, et al.
Published: (2025)
A De Novo Mutation (c.2423A>G) in SAMD9 Causing MIRAGE Syndrome With Intrauterine Growth Retardation and Renal Hypoplasia in a Chinese Family
by: Yuxin Huang, et al.
Published: (2026)
by: Yuxin Huang, et al.
Published: (2026)
Unveiling enantioselective mechanisms of toxicity of butylone in Daphnia magna.
by: Vidal, Renata, et al.
Published: (2025)
by: Vidal, Renata, et al.
Published: (2025)
Genome‐Wide Cross‐Trait Analysis Dissects the Shared Genetic Architecture Between Type 2 Diabetes Mellitus and Metabolic Dysfunction–Associated Steatotic Liver Disease
by: Zijun Zhu, et al.
Published: (2026)
by: Zijun Zhu, et al.
Published: (2026)
Novel Variants in the SLC16A2 Gene Associated With Allan–Herndon–Dudley Syndrome in China
by: Wei Li, et al.
Published: (2026)
by: Wei Li, et al.
Published: (2026)
Novel ABCG5 and ABCG8 Variants in Sitosterolemia: Insights Into Haemolysis, Calcium Dysregulation and Therapeutic Challenges
by: Prashant Warang, et al.
Published: (2026)
by: Prashant Warang, et al.
Published: (2026)
Epithelial Cell–Specific Prognostic Signature (FTH1, RIT1, WASL, NDRG2, KIFC3) Stratifies Cervical Cancer Patients and Correlates With Immune Infiltration
by: Xuegu Wang, et al.
Published: (2026)
by: Xuegu Wang, et al.
Published: (2026)
Similar Items
-
A transient mutational burst occurs during yeast colony development.
by: Agier, Nicolas, et al.
Published: (2025) -
Functional roles of mastigonemes in Ectocarpus gamete swimming revealed by CRISPR-Cas9 mutagenesis.
by: Harada, Minori, et al.
Published: (2026) -
Mutational features of chromids and chromosomes in provide new insights into the evolution of secondary replicons.
by: Jiang, Wanyue, et al.
Published: (2025) -
The negligible mutagenic effects of norfloxacin on the genome of the fission yeast ATCC-16979.
by: Lin, Tongtong, et al.
Published: (2025) -
Determination of leachate toxicity through acute toxicity using Daphnia pulex and anaerobic toxicity assays
by: Y. S. Carabalí-Rivera
Published: (2017)