Results 331 to 340 of about 133,619 (388)

Prenatal ultrasound diagnosis of ectopic ureter and renal hypoplasia in two puppies: a case report. [PDF]

Vet Res Commun
Moserová H, Frgelecová L, Morávek R, Proks P.   +3 more
europepmc   +1 more source

Substance Use Right Before or During Work Among the Young US Workers: Evidence From the National Longitudinal Survey of Youth 1997 Cohort

American Journal of Industrial Medicine, EarlyView.
ABSTRACT Objective Substance use right before or during work (hereinafter, “substance use in the workplace”) poses significant health risks to users, colleagues, and the public in the workplace. However, less clear are figures on recent prevalence, characteristics of those engaging in such behaviors, and variations across occupations.
Sehun Oh, Daejun Park, Sarah Al‐Hashemi   +2 more
wiley   +1 more source

Comparison Between Two Methodologies of Sample Preservation for RNA Extraction in Naturally Delivered Ovine Placenta. [PDF]

Animals (Basel)
Aránguiz F, Bahamonde J, Sales F, Araya M, Ulloa-Leal C, Ratto M, Sandoval C.   +6 more
europepmc   +1 more source

Phenotypical Characterization of Gastroenterological and Metabolic Manifestations in Patients With Williams–Beuren Syndrome

American Journal of Medical Genetics Part A, Volume 197, Issue 6, June 2025.
ABSTRACT Gastrointestinal (GI) symptoms are common in patients with Williams–Beuren syndrome (WBS), but their prevalence and possible causes are not yet fully known. This study assessed GI symptoms' prevalence and their possible origin by performing a predefined set of tests in adult WBS patients.
Maria Francesca Bedeschi, Annarita Baldassarri, Roberta Villa, Federico Tanzi, Simona Salera, Vincenza Lombardo, Alessandro Draghi, Nicole Piazza O'Sed, Giovanni Casazza, Maurizio Vecchi, Mirella Fraquelli   +10 more
wiley   +1 more source

Small Ruminant Parturition Detection Based on Inertial Sensors-A Review. [PDF]

Animals (Basel)
Gonçalves P, Marques MR, Nyamuryekung'e S, Jorgensen GHM.   +3 more
europepmc   +1 more source

Functional Analyses of SATB2 Variants Reveal Pathogenicity Mechanisms Linked With SATB2‐Associated Syndrome

American Journal of Medical Genetics Part A, Volume 197, Issue 6, June 2025.
ABSTRACT SATB2‐associated syndrome (SAS) is characterized by intellectual disability, neurodevelopmental disorders, cleft palate, and dental abnormalities. SAS is caused by variants in the special AT‐rich sequence‐binding protein 2 (SATB2), which encodes a transcription factor containing two CUT domains and a homeobox (HOX) domain.
Nao Ukita, Takuya Ogawa, Mamiko Yamada, Chisen Takeuchi, Kenjiro Kosaki, Keiji Moriyama   +5 more
wiley   +1 more source

The Milk Compositions and Blood Parameters of Lactating Dezhou Donkeys Changes With Lactation Stages. [PDF]

Vet Med Sci
Zhou M, Ma Z, Du X, Wang C, Liu G.
europepmc   +1 more source

Phenotypic Expansion of Knobloch Syndrome Type 2 in an Individual With a De Novo PAK2 Variant

American Journal of Medical Genetics Part A, Volume 197, Issue 6, June 2025.
ABSTRACT P21‐activated kinase 2 (PAK2) is a serine/threonine kinase essential for a variety of cellular processes including signal transduction, cellular survival, proliferation, and migration. A recent report proposed monoallelic PAK2 variants cause Knobloch syndrome type 2 (KNO2)—a developmental disorder primarily characterized by ocular anomalies ...
Elizabeth A. Werren, Louisa Kalsner, Jessica M. Ewald, Michael Peracchio, Cameron King, Purva Vats, Peter A. Audano, Peter N. Robinson, Mark D. Adams, Melissa A. Kelly, Adam P. Matson   +10 more
wiley   +1 more source

Hair Allopregnanolone in Mares and Foals as a Retrospective Biomarker of Predicting Feto-Maternal Well-Being. [PDF]

Animals (Basel)
Ellero N, Lanci A, Mariella J, van den Boom R, Cotticelli A, Peric T, Prandi A, Freccero F, Castagnetti C.   +8 more
europepmc   +1 more source

Clinical Insights Into Nabais Sá‐De Vries Syndrome due to a Novel SPOP Mutation: Neuromotor, Cognitive, Adaptive, Behavioral, and Neurovisual Features

American Journal of Medical Genetics Part A, Volume 197, Issue 6, June 2025.
ABSTRACT Nabais Sá‐De Vries syndrome (NSDVS) is an extremely rare autosomal dominant disorder caused by SPOP mutations. To date, only 10 cases have been described presenting with intellectual disability, neurological signs and symptoms, and a variable association of dysmorphic features.
Jessica Galli, Erika Loi, Federica Zanardini, Giovanna Baldoni, Francesca Novara, Serena Panigada, Roberto Ciccone, Maria Rosa Cutrì, Alice Bertoletti, Lorenzo Pinelli, Elisa Fazzi   +10 more
wiley   +1 more source