Pleiotropic functions of the tumor- and metastasis-suppressing matrix metalloproteinase-8 in mammary cancer in MMTV-PyMT transgenic mice by Julie Decock (44558)

“…We have intercrossed Mmp8-null mice with the Polyoma virus middle T oncogene-driven (MMTV-PyMT) mouse model of mammary cancer to explore the effects of loss of MMP-8 on the incidence and progression of mammary carcinomas. …”

Resveratrol-Elicited PKC Inhibition Counteracts NOX-Mediated Endothelial to Mesenchymal Transition in Human Retinal Endothelial Cells Exposed to High Glucose by Roberta Giordo (299595)

“…Treatment of HRECs with HG increased intracellular ROS levels and promoted phenotype shifting towards EndMT, evidenced by decreased expression of endothelial markers concomitant with increased expression of mesenchymal ones. …”

ACTB Loss-of-Function Mutations Result in a Pleiotropic Developmental Disorder by Sara Cuvertino (18892069)

Simultaneous Bilateral Neck of Femur Fracture in a Young Adult with Underlying Metabolic Disturbances by Eslam Alkaramani (14570439)

“…Simultaneous bilateral fractures of the femoral neck are considered very rare injuries. Few cases were reported in the literature. …”

Automated detection of posterior urethral valves in voiding cystourethrography images: A novel AI-Based pipeline for enhanced diagnosis and classification by Saidul Kabir (15302407)

“…<h3>Introduction </h3><p dir="ltr">Posterior Urethral Valves (PUV) are rare congenital anomalies of the male urinary tract that can lead to urethral obstruction and increased risk of kidney disease. …”

A dramatized method for teaching undergraduate students responsible research conduct by Kuei-Chiu Chen (14108854)

“…Unfortunately, these experiences rarely include training in science or research ethics. …”

Acute spasticity in malignant MCA stroke: a case report and review of literature by Muhammad Faizan (12710607)

“…However, an acute onset of spasticity at presentation is extremely rare. We report a case of a 40-year-old male patient who presented with spasticity accompanied by aphasia and decreased consciousness. …”

A Severe Case of Overlap of Morphea and Eosinophilic Fasciitis after Burn Injuries by Hania Sami (21436013)

“…<h3>Background</h3><p dir="ltr">Generalized morphea is a rare fibrosing skin illness that progresses from erythematous, violet‐colored skin patches to sclerotic plaques. …”

Light chain amyloidosis presenting with autoimmune hepatitis-primary sclerosing cholangitis overlap syndrome by Hammad Shabir Chaudhry (20376378)

“…Her liver enzymes (Alkaline phosphatase, Alanine aminotransferase, Aspartate aminotransferase had decreased significantly.</p><h3>Conclusions</h3><p dir="ltr">AL amyloidosis can very rarely present as AIH-PSC overlap syndrome, manifesting with raised liver enzymes, biliary strictures, pruritis and positive liver antibodies. …”

Successful minimally invasive management of nonvascular grade IV blunt renal trauma with complete transection in a 7-year-old girl by Zlatan Zvizdic (9212371)

“…Although such injuries have a decreased likelihood of spontaneous resolution, not all require open operative repair. …”

Understanding the Molecular Mechanisms of Dysglycemia in Patients with Fanconi-Bickel Syndrome by Sanaa Ali Sharari (19953093)

“…<p dir="ltr">Fanconi–Bickel Syndrome (FBS) is a rare disorder of carbohydrate metabolism that is characterized mainly by the accumulation of glycogen in the kidney and liver. …”

Fanconi–Bickel Syndrome: A Review of the Mechanisms That Lead to Dysglycaemia by Sanaa Sharari (12561952)

“…Dysfunctional mutations and decreased GLUT2 expression leads to dysglycaemia (fasting hypoglycemia, postprandial hyperglycemia, glucose intolerance, and rarely diabetes mellitus), hepatomegaly, galactose intolerance, rickets, and poor growth. …”

Clinical and Biochemical Analysis of Glutamate-Cysteine Ligase Deficiency Presented with Late-Onset Spinocerebellar Ataxia and Hemolytic Anemia by Mohammed Al-Hatou (22225603)

“…Its deficiency is reported to cause hemolysis of variable severity and is a rare cause of neurological abnormalities such as spinocerebellar ataxia. …”

Mirizzi Syndrome: Mastering the Challenge, Characterization and Management Outcomes in a Retrospective Study of 60 Cases by Yousef Yahia (19756989)

“…<h3>Background</h3><p dir="ltr">Mirizzi Syndrome (MS) is a rare complication of gallstone disease that poses diagnostic and management challenges.…”

PGAP3 Associated with Hyperphosphatasia with Mental Retardation Plays a Novel Role in Brain Morphogenesis and Neuronal Wiring at Early Development by Sahar I. Da’as (9631717)

“…<p dir="ltr">Recessive mutations in Post-GPI attachment to proteins 3 (PGAP3) cause the rare neurological disorder hyperphosphatasia with mental retardation syndrome 4 type (HPMRS4). …”

Evidence-based safety education and training for traffic injury prevention by Abbas Motevalian (338825)

“…Review of the systematic reviews show that education only interventions are rarely effective on prevention of road traffic crashes. …”

Deep Learning for Dynamic Wildlife Monitoring: A Real-Time Approach by Abdul Basit Mughal (22929001)

“…<p dir="ltr">With the rapid amount of deforestation around the world, wild animals lose their habitat and move closer to human settlements, leading to increased human-wildlife conflict and the loss of important human lives, livestock, and rare wild animal species. Wildlife monitoring is an essential task in computer vision for maintaining biodiversity, ecosystem balance and stability. …”

Chiropractic manipulations gone wrong by Nature Research (16552612)

“…Simultaneous dissection of several neck arteries however — as was the case with the patient in Qatar — is rare. Barbers and massage parlours in the Middle East often offer neck manipulation to relieve neck pain. …”

Fetoplacental transmission and placental response to SARS-CoV-2: Evidence from the literature by Henry C. Ezechukwu (13253406)

“…Out of 45 eligible studies identified, 24 (53.34%) showed no evidence of vertical transmission, 15 (33.33%) supported the hypothesis of very rare, low possibility of vertical transmission and 6 (13.33%) were indecisive and had no comment on vertical transmission. …”

Genome-wide association study and meta-analysis of phytosterols identifies a novel locus for serum levels of campesterol by Jamil Mahmoud Alenbawi (21546995)

“…<p dir="ltr">Sitosterolemia is a rare inherited disorder caused by mutations in the <i>ABCG</i>_<em>5</em>/<i>ABCG8</i> genes. …”