Results 1 to 10 of about 84,871 (291)

Skeletal Anomalies in Senegalese Sole (Solea senegalensis, Kaup) Fed with Different Commercial Enriched Artemia: A Study in Postlarvae and Juveniles [PDF]

Animals, 2020
The high incidence of skeletal anomalies in Senegalese sole (Solea senegalensis) still constitutes a bottleneck constraining its production. There are diverse commercially available products for the enrichment of live preys, but few reports of their ...
Ana Manuela de Azevedo, Ana Paula Losada, Isabel Ferreiro, Ana Riaza, Vanesa Losada, Tommaso Russo, Clara Boglione, Sonia Vázquez, María Isabel Quiroga   +8 more
doaj   +2 more sources

Effects of the Interaction between Dietary Vitamin D₃ and Vitamin K₃ on Growth, Skeletal Anomalies, and Expression of Bone and Calcium Metabolism-Related Genes in Juvenile Gilthead Seabream (Sparus aurata) [PDF]

Animals
The interaction between vitamin D and vitamin K is crucial for regulating bone metabolism and maintaining calcium homeostasis across diverse animal species due to their complementary roles in calcium metabolism and bone health.
Ulaganathan Sivagurunathan, Marisol Izquierdo, Yiyen Tseng, Philip Antony Jesu Prabhu, María Jesús Zamorano, Lidia Robaina, David Domínguez   +6 more
doaj   +2 more sources

Early Nutrition Impacts on Growth, Skeletal Anomalies and Organ Ontogeny in Larval Atlantic Cod (Gadus morhua) [PDF]

Animals
Early life nutrition is a critical factor influencing subsequent performance and quality, including skeletal development, in farmed Atlantic cod (Gadus morhua). This study investigated the effects of a novel start-feed protocol utilizing barnacle nauplii
Joana Pedro, João Henriques, Maria Bergvik, Konstantinos Tzakris, Michael Viegas, Katerina Loufi, Jorge M. O. Fernandes, Benjamín Costas, Nils Tokle, Luís E. C. Conceição   +9 more
doaj   +2 more sources

Application of trio-based whole-exome sequencing in fetal ultrasound anomalies: a single-center retrospective study of 454 cases [PDF]

Frontiers in Genetics
This study assessed the diagnostic effectiveness of trio-WES compared to CMA in fetuses with ultrasound anomalies and explored optimal prenatal testing strategies. A retrospective review included 454 fetuses who underwent trio-WES and/or CMA between 2020
Dongyi Yu, Dongyi Yu, Dongyi Yu, Dairong Feng, Dairong Feng, Dairong Feng, Jiangbo Qu, Jiangbo Qu, Jiangbo Qu, Lei Nie, Qian Liu, Lu Gao, Lu Gao, Lu Gao, Wenzhen An, Na Liu, Na Liu, Na Liu, Yuying Fang, Yuying Fang, Yuying Fang   +20 more
doaj   +2 more sources

Skeletal anomaly monitoring in rainbow trout (Oncorhynchus mykiss, Walbaum 1792) reared under different conditions. [PDF]

PLoS ONE, 2014
The incidence of skeletal anomalies could be used as an indicator of the "quality" of rearing conditions as these anomalies are thought to result from the inability of homeostatic mechanisms to compensate for environmentally-induced stress and/or altered
Clara Boglione, Domitilla Pulcini, Michele Scardi, Elisa Palamara, Tommaso Russo, Stefano Cataudella   +5 more
doaj   +5 more sources

Frequency of skeletal anomalies in fetal and neonatal autopsies [PDF]

Medicinski Podmladak, 2021
Introduction: Skeletal anomalies are a heterogeneous group of disorders including changes in bone shape, size, and density that cause abnormalities of the extremities, trunk, and head.
Radojević Matija, Pjevčević Katarina, Putniković Dunja, Jevtić Jovan, Simić Ljubica   +4 more
doaj   +1 more source

Prevalence of Dental Anomalies in Skeletal Malocclusions with Different Growth Patterns in North Indian Population-A Cross-sectional Study [PDF]

Journal of Clinical and Diagnostic Research, 2021
Introduction: Anomalies of the developing dentition occur due to absence or interruption of normal tooth development along with genetic and/or environment influences.
FLORET JOSE, MANINDER S SIDHU, ASHISH DABAS, SEEMA GROVER, NAMRATA DOGRA   +4 more
doaj   +1 more source

Case report: Extending the spectrum of clinical and molecular findings in FOXC1 haploinsufficiency syndrome

Frontiers in Genetics, 2023
FOXC1 is a ubiquitously expressed forkhead transcription factor that plays a critical role during early development. Germline pathogenic variants in FOXC1 are associated with anterior segment dysgenesis and Axenfeld-Rieger syndrome (ARS, #602482), an ...
Alexandra Garza Flores, Alexandra Garza Flores, Ida Nordgren, Maria Pettersson, Maria Pettersson, Dora Dias-Santagata, Daniel Nilsson, Daniel Nilsson, Anna Hammarsjö, Anna Hammarsjö, Anna Lindstrand, Anna Lindstrand, Dominyka Batkovskyte, Janey Wiggs, David S. Walton, Paula Goldenberg, Jesper Eisfeldt, Jesper Eisfeldt, Angela E. Lin, Ralph S. Lachman, Ralph S. Lachman, Ralph S. Lachman, Gen Nishimura, Gen Nishimura, Giedre Grigelioniene, Giedre Grigelioniene, Giedre Grigelioniene   +26 more
doaj   +1 more source

Klippel-Feil syndrome with multiple skeletal anomalies, Dandy-Walker spectrum, and occipital cephalocele—a rare presentation

The Egyptian Journal of Radiology and Nuclear Medicine, 2021
Background Klippel-Feil syndrome (KFS) is a congenital malformation causing fusion of at least two cervical vertebrae and characterized clinically by presence of triad of short neck, limited neck movements, and low posterior hair line.
Mohammad Shoaib, M. Sarthak Swarup, Gaurav Pradhan   +2 more
doaj   +1 more source

Associations across 22 dental and craniovertebral anomalies or variations, sagittal skeletal relationships, and vertical growth patterns: a comprehensive epidemiological study of 43 dentoskeletal traits

BMC Oral Health, 2023
Introduction Despite researchers' recent interest in identifying links between some dental and craniovertebral abnormalities, there are many important, unassessed gaps in our knowledge of this matter. In addition, previous samples were small.
Farhad Sobouti, Sepideh Dadgar, Parsa Goleyjani, Vahid Rakhshan   +3 more
doaj   +1 more source