Results 281 to 290 of about 135,794 (322)

Acrylamide Impacts on Black Soldier Fly Larvae: Growth, Toxicity, Microbes, and Bioaccumulation Risks for Food/Feed Safety. [PDF]

Insects
Hao J, Yang J, Zhang Y, Zhao S, Liu S, Hu W.   +5 more
europepmc   +1 more source

AP2M1 Is a Candidate Gene for Microcephaly and Intellectual Disability in 3q27.1 Deletions

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Deletions of the 3q26.33q27.2 region appear to correlate with a distinct phenotype, although there are few reported cases. Here, we present seven previously unreported individuals carrying de novo 3q27 deletions (under 5 Mb), which include the AP2M1 (adaptor‐related protein complex 2, mu‐1 subunit) gene and summarize data from 12 previously ...
Russell Gear, Paul Kalitsis, Melissa Glass, Bertrand Isidor, Catherine Vincent‐Delorme, Florence Petit, Judith M. A. Verhagen, Alexander Jorge, Ana Cristina Victorino Krepischi, Ikeoluwa Osei‐Owusu, Eva Martinez, Anne O'Donnell‐Luria, Nicole de Leeuw, Sarah Ruggiero, Ingo Helbig, Francis David I, Natasha J. Brown   +16 more
wiley   +1 more source

Neuroaxonal Dystrophy With Osteopetrosis Associated With a Novel Biallelic Nonsense Homozygous Variant in BORCS5

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Neuroaxonal dystrophy (NAD) with osteopetrosis syndrome (OMIM # 600329) was first reported in a consanguineous Moroccan Jewish family. However, to date, no genetic variant has been linked to this disease. We report on sibs, born to consanguineous Pakistani parents identified prenatally with cerebral ventriculomegaly and agenesis of the corpus ...
Yael Fisher, Orli Greenberg, Patrick Shannon, Andrea Staines, Bobbi McGivern, Melanie Patricia Napier, David Chitayat   +6 more
wiley   +1 more source

WormRACER: Robust Analysis by Computer-Enhanced Recording. [PDF]

Geroscience
Van Camp BT, Zapata QN, Curran SP.
europepmc   +1 more source

Artificial Intelligence Software Changes Rare Disease Testing Strategy in Real Time: An International Case Series Using Face2Gene

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Genetic disorders commonly share features such as developmental delays, cognitive impairment, and behavioral challenges, yet many conditions also present unique dysmorphic features that distinguish them. Performing a thorough medical and family history and a detailed physical exam with attention to dysmorphic features is often the first step ...
Natasha L. Rudy, Adriana Gomes, Tinatin Tkemaladze, Omar Abdul‐Rahman, Drew Cratsenberg, Giulia Pascolini, Giovanni Di Zenzo, Daniele Castiglia, Emily Black, Camerun Washington, Lauren Chad, Cynthia Curry, Miguel Del Campo, Nicole Fleischer, Lynne M. Bird, Anna C. E. Hurst   +15 more
wiley   +1 more source

Maggots crawling on the eyeball; a case of external ocular myiasis. [PDF]

Am J Ophthalmol Case Rep
Jalink MB, Stijnis K.
europepmc   +1 more source

Soft and flexible robot skin actuator using multilayer 3D pneumatic network. [PDF]

Nat Commun
Shin HG, Chung WK, Kim K.
europepmc   +1 more source

Exploring Developmental Connections: Sleep Patterns, Self-Locomotion, and Vocabulary Growth in Early Childhood. [PDF]

Infancy
Belia M, Vihman M, Keren-Portnoy T.
europepmc   +1 more source

Sensing-actuating integrated asymmetric multilayer hydrogel muscle for soft robotics. [PDF]

Microsyst Nanoeng
Zhou Y, Zhao Y, Zhao D, Guan X, Zhang K, Pi Y, Zhong J.   +6 more
europepmc   +1 more source

Role of dopamine in responsiveness to acute ethanol exposure in <i>Caenorhabditis elegans</i>. [PDF]

MicroPubl Biol
Gayadin D, Prunty M, Fretham SJ.
europepmc   +1 more source