Results 221 to 230 of about 156,625 (312)

QTL mapping of key phenological and morphological traits in grain amaranth (<i>Amaranthus hypochondriacus</i> L.). [PDF]

Breed Sci
Zaelani A, Isobe S, Shirasawa K, Yoshioka Y.   +3 more
europepmc   +1 more source

Integrative utilization of genomic resources for improved phylogenetic resolution in Sonerileae (Melastomataceae)

American Journal of Botany, EarlyView.
Abstract Premise Advances in new next‐generation sequencing (NGS) methods have revolutionized phylogenetics, yet challenges remain in effectively utilizing data from a wide range of sources. A well‐resolved and broadly sampled phylogeny for Sonerileae, the second‐largest tribe in Melastomataceae, is still lacking, hindering our understanding of its ...
Luo Chen, Marie Claire Veranso‐Libalah, J. Peter Quakenbush, Ying Liu, Fabián A. Michelangeli, Diego F. Morales‐Briones, Gudrun Kadereit   +6 more
wiley   +1 more source

Genetic Diversity and Marker-Trait Associations in Commercial Cultivars and Weedy <i>Perilla frutescens</i> from South Korea and Japan Based on Morphological Traits and SSR Markers. [PDF]

Plants (Basel)
Lee DH, Cho J, Park H, Heo TH, Lee JK.
europepmc   +1 more source

Pollination by long‐proboscid horseflies and its implications for reproductive isolation among coflowering Satyrium orchids in South Africa

American Journal of Botany, EarlyView.
Abstract Premise Floral adaptations to pollinators can drive lineage diversification and promote coexistence of species. We investigated the reproductive biology of Satyrium longicolle, a South African orchid that we hypothesized to belong to a long‐proboscid horsefly pollination guild and examined overlap of pollinators and floral traits among ...
Steven D. Johnson, Matthew Moir, Ethan Newman, Timotheüs Van der Niet   +3 more
wiley   +1 more source

Resistance mechanisms in collard green genotypes to Plutella xylostella: role of physical and morphological traits. [PDF]

Pest Manag Sci
Pinheiro AM, Baldin ELL, Canassa VF, da Silva Santana A, Dos Santos TLB, Lourenção AL, Raetano CG.   +6 more
europepmc   +1 more source

Genomic Contributors to Congenital Diaphragmatic Hernia: Results of Exome Sequencing in 560 Probands and Cross Reference of Findings in an Independent Cohort

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT There is a strong genetic contribution to the etiology of congenital diaphragmatic hernia (CDH). This study evaluated genetic testing results and diagnostic yield for fetuses and children with CDH. This was a retrospective cohort study of exome sequencing (ES) performed at GeneDx for fetuses and children ≤ 18 years of age with CDH compared ...
Justin Blair, Kevin Carratu, Natalie E. Rintoul, Holly L. Hedrick, William H. Peranteau, Catherine M. Avitabile, Kirsty McWalter, Paul Kruszka, Ian D. Krantz, K. Taylor Wild   +9 more
wiley   +1 more source

Integrated chemometric evaluation of morphological traits, chemical composition, and hepatotoxicity of <i>Polygonum multiflorum</i>. [PDF]

Front Pharmacol
Li Y, Wang Q, Yang Y, Huang X, Zhang Y.
europepmc   +1 more source

Electrocardiographic and Skin Manifestations of Turner Syndrome: Association With Cardiovascular Disease

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Congenital heart disease (CHD) and dermatologic conditions such as lymphedema and acquired melanocytic nevi (AMN) are common in Turner Syndrome (TS). We hypothesized that abnormalities of cranial neural crest cell derivatives drive the skin and heart manifestations of TS. We conducted joint cardiac and skin examinations of volunteers at a 2023
Sarah Elsaim, Brett Vernier, Van Thi Thanh Truong, Riya T. Patel, Matthew Brown, Martin Chacon Portillo, Megan Rogge, David Rodriguez‐Buritica, Siddharth K. Prakash   +8 more
wiley   +1 more source

Genetic variation of barley genotypes using morphological traits, amylose content, and molecular markers. [PDF]

Sci Rep
Aka SR, Sarker U, Talukder MZA, Azam MG, Ercisli S, Hossain N, Alharbi MS, Ullah R.   +7 more
europepmc   +1 more source

Distinct Neuropsychiatric Profiles Associated With 17p11.2 Deletions and RAI1 Variants in Smith–Magenis Syndrome

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Smith–Magenis syndrome (SMS) results from either a recurrent 17p11.2 deletion or pathogenic variants in the retinoic acid induced 1 gene (RAI1). While neurodevelopmental impairment and behavioral dysregulation are well recognized, systematic genotype‐stratified analyses across psychiatric domains remain limited.
Albin Blanc, Christophe Nemos, Céline Bonnet, Mathilde Renaud, Sandra Chapuis, Pauline Boiroux, Marie‐Noëlle Babinet, Caroline Demily   +7 more
wiley   +1 more source