Results 211 to 220 of about 1,467,829 (302)

An Atypical Root Canal Configuration of Maxillary Second Molar: A Case Report. [PDF]

J Dent (Shiraz)
Rezaei Nejad A, Ghahramani Y, Alimardani F, Hosseini H.   +3 more
europepmc   +1 more source

Root canal anatomy of third molars

Journal of dental research, 2008
Vodanović, Marin, Njemirovskij, Vera, Njemirovskij, Zdenko, Galić, Nada   +3 more
openaire   +1 more source

Evolutionary history and taxonomy of the genus Zea

American Journal of Botany, EarlyView.
Abstract Premise Taxonomic differentiation of teosinte species (Zea spp.), the closest relatives of maize (Z. mays) is crucial for understanding their distribution, ecology, and evolutionary history. Resolving the taxonomic uncertainties is of scientific interest and has practical implications for biodiversity management, preservation, and utilization.
José de Jesús Sánchez González, Lino De La Cruz Larios, José A. Ruiz‐Corral, Benjamín Hernández, Diana M. Rivera‐Rodríguez   +4 more
wiley   +1 more source

A Consensus-Based Glossary for Controversial Terminology in Root and Canal Anatomy. [PDF]

Int Endod J
Ahmed HMA, Nagendrababu V, Keleş A, Wolf TG, Duncan HF, Peters OA, Dummer PMH, Delphi Group for Terminology in Root Canal Anatomy.   +7 more
europepmc   +1 more source

Heterozygous Variants in LRP1 Cause a Neurodevelopmental Disorder With Congenital Heart Defects

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT LRP1 encodes the low‐density lipoprotein (LDL) receptor‐related protein 1 (LRP1), a transmembrane protein involved in endocytosis and activation of multiple signaling pathways. LRP1 variants have been implicated in the pathogenesis of congenital heart defects (CHD), Alzheimer's disease, and neurodevelopmental disorders (NDD).
Alyssa L. Rippert, Gudny Anna Arnadottir, Laura Bedinger, Nicola Brunetti‐Pierri, Jennifer Cech, Xin Chen, Yanmin Chen, Erika Chick, Sarah Dyack, Madeleine Franchi, Tanja Frey, David Genevieve, Ian Glass, Jorge Granadillo, Kelly A. Keener, Sara B. MacKay, Paige McDunnah, Vinod K. Misra, Kristin G. Monaghan, Sureni V. Mullegama, Cristina Peduto, Leia Peterman‐Prather, Anita Rauch, Cherith Somerville, Kari Stefansson, Katharina Steindl, Patrick Sulem, Telma Sulem, Pamela Trapane, Roberta Zeuli, Samuel Zinner, Kosuke Izumi   +31 more
wiley   +1 more source

A Rare Form of Microcephalic Primordial Dwarfism due to NSMCE2 Deficiency (Seckel Syndrome Type 10): A Report of Macular Involvement

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Biallelic variants in NSMCE2 (MMS21), which encodes the SUMO E3 ligase subunit of the SMC5/6 chromatin‐maintenance complex, have recently been implicated in microcephalic primordial dwarfism (MPD), corresponding to Seckel syndrome type 10 (OMIM #617246).
Cristina Peduto, Céline Huber, Clément Paya, Isabelle Audo, Nathalie Boddaert, Valérie Cormier‐Daire   +5 more
wiley   +1 more source

Unusual Root Canal Morphology in Mandibular Molars: A Case Series. [PDF]

Cureus
Mohan S, Chaudhury A, Thomas G, Jose S, Aboobacker S.   +4 more
europepmc   +1 more source

Expanding the Phenotypic Spectrum of TXNDC15‐Related Ciliopathies to Include Joubert Syndrome

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Biallelic loss‐of‐function variants in TXNDC15 are a known cause of the perinatally lethal ciliopathy Meckel syndrome (MKS). TXNDC15 encodes an endoplasmic reticulum (ER)‐resident thioredoxin‐domain protein required for ciliary transition zone integrity.
Zachary T. Sentell, Robert Geraghty, Juliana E. Arcila‐Galvis, Praveen Dhondurao‐Sudhindar, Sergio Foullerat Cañada, Fulvio D'Abrusco, Bosanka Jocic‐Jakubi, Miguel Barroso‐Gil, Valentina Serpieri, Thomas M. Kitzler, Kate E. Chandler, Eleanor G. Seaby, Gabrielle Wheway, Jennifer C. Dempsey, Dan Doherty, Enza M. Valente, John A. Sayer   +16 more
wiley   +1 more source

Endodontic Management of a Mandibular Central Incisor With Vertucci Type V Configuration: A Case Report From Nepal. [PDF]

Clin Case Rep
Phuyal B, Shrestha N.
europepmc   +1 more source