Procainamide–SAHA Fused Inhibitors of hHDAC6 Tackle Multidrug-Resistant Malaria Parasites by Flore Nardella (4821411)

bta-miR-484 Inhibits Bovine Intramuscular Adipogenesis by Regulating Mitotic Clonal Expansion via the MAP3K9/JNK/CCND1 Axis by Xinhao Ma (11795429)

Additional examples—Boundary vector cells. by Lear Cohen (15353793)

bta-miR-484 Inhibits Bovine Intramuscular Adipogenesis by Regulating Mitotic Clonal Expansion via the MAP3K9/JNK/CCND1 Axis by Xinhao Ma (11795429)

bta-miR-484 Inhibits Bovine Intramuscular Adipogenesis by Regulating Mitotic Clonal Expansion via the MAP3K9/JNK/CCND1 Axis by Xinhao Ma (11795429)

bta-miR-484 Inhibits Bovine Intramuscular Adipogenesis by Regulating Mitotic Clonal Expansion via the MAP3K9/JNK/CCND1 Axis by Xinhao Ma (11795429)

Different models. by Ying Shi (115282)

miR-190 Enhances HIF-Dependent Responses to Hypoxia in <i>Drosophila</i> by Inhibiting the Prolyl-4-hydroxylase Fatiga by Ana Laura De Lella Ezcurra (2806105)

Comparing Tolerability and Efficacy of Generic versus Brand Alendronate: A Randomized Clinical Study in Postmenopausal Women with a Recent Fracture by Joop P. W. van den Bergh (474666)

“…However, for subscale abdominal pain, patients using generic had a significantly higher mean GSRS score at week 4 (estimated mean difference (B): 0.40; 95%CI: 0.05 to 0.74, p = 0.024). …”

Economic evaluation of brief cognitive behavioural therapy for social activation in recent-onset psychosis - Fig 2 by Ben F. M. Wijnen (4997315)

“…<p>a) Cost-effectiveness plane of QALY scores at 6 months’ follow-up (costs per QALY gained); Fig 2B) Cost-effectiveness plane of responder rate (≥5 decrease in PANSS score) at 6 months’ follow-up (costs per extra responder). …”

Neoadjuvant envafolimab in a patient with MSI-H/dMMR colon cancer: a case report and literature review by Ziwei Chen (626412)

“…A 36-year-old man suffered from repeated illness of right upper quadrant for over 1 year, and the illness were not recovered after 10 days of oral Changyanning tablet. …”

Interactions of organic acids with <i>Campylobacter coli</i> from swine by Ross C. Beier (441557)

“…<div><p><i>Campylobacter coli</i> is a bacterial species that is a major cause of diarrheal disease worldwide, and <i>Campylobacter</i> spp. are among the top 5 foodborne pathogens in the United States. …”

Datasheet1_A Canadian, retrospective, multicenter experience with selexipag for a heterogeneous group of pediatric pulmonary hypertension patients.pdf by David Youssef (14686570)

“…</p>Results<p>Twenty-four pediatric patients (fifteen female) with a mean age of 9.7 (range 2.0–15.5) years were included. …”

Angpt1 deficiency increased vascular rarefaction after UUO. by Krishnapriya Loganathan (4729575)

“…<p>(A) Vessel area in renal cortex was estimated from endomucin staining correlated to nuclei number at all time points after UUO. …”

Supplementary Material for: Off-label Use of Mycophenolate Mofetil in Immunoglobulin A Nephropathy: A Systematic Review and Meta-analysis by Feng L. (5056958)

3D-Printed Complex Microstructures with a Self-Sacrificial Structure Enabled by Grayscale Polymerization and Ultrasonic Treatment by Yibo Liao (6812618)

Comparative pharmacokinetics and pharmacodynamics of the advanced Retinol-Binding Protein 4 antagonist in dog and cynomolgus monkey by Boglarka Racz (1336803)

3D-Printed Complex Microstructures with a Self-Sacrificial Structure Enabled by Grayscale Polymerization and Ultrasonic Treatment by Yibo Liao (6812618)

Image_2_A Mutation in VWA1, Encoding von Willebrand Factor A Domain-Containing Protein 1, Is Associated With Hemifacial Microsomia.TIF by Yibei Wang (5321825)

“…Background<p>Hemifacial microsomia (HFM) is a type of rare congenital syndrome caused by developmental disorders of the first and second pharyngeal arches that occurs in one out of 5,600 live births. …”

Image_1_A Mutation in VWA1, Encoding von Willebrand Factor A Domain-Containing Protein 1, Is Associated With Hemifacial Microsomia.TIF by Yibei Wang (5321825)

“…Background<p>Hemifacial microsomia (HFM) is a type of rare congenital syndrome caused by developmental disorders of the first and second pharyngeal arches that occurs in one out of 5,600 live births. …”