Maternally transmitted extra ring (21) chromosome in a boy with Down's syndrome

Factors secreted from dental pulp stem cells show multifaceted benefits for treating experimental temporomandibular joint osteoarthritis.

Osteoarthritis and cartilage·2020

eNOS plays an important role in the regulation of colonic inflammation: a novel therapeutic target and a predictive marker for the prognosis of ulcerative colitis.

Free radical research·2014

KRAS mutations in primary tumours and post-FOLFOX metastatic lesions in cases of colorectal cancer.

British journal of cancer·2012

Effects of transglucosidase on diabetes, cardiovascular risk factors and hepatic biomarkers in patients with type 2 diabetes: a 12-week, randomized, double-blind, placebo-controlled trial.

Diabetes, obesity & metabolism·2011

KRAS mutations detected by the amplification refractory mutation system-Scorpion assays strongly correlate with therapeutic effect of cetuximab.

British journal of cancer·2011

The effectiveness of packed therapy with three drugs in Helicobacter pylori eradication in Japan.

Methods and findings in experimental and clinical pharmacology·2010

Clinical and zebrafish studies of truncating SF3B2-variants in craniofacial microsomia.

Human genetics·2026

CRISPR/Cas9-based repair of a heterozygous HNF1A mutation in patient-derived hiPSCs.

Human genetics·2026

TTC14 dysfunction contributing to microcephaly and lissencephaly spectrum features through protein mislocalization and impaired RNA processing.

Human genetics·2026

The Russian FSHD registry: a first look at the cohort.

Human genetics·2026

Genetic ancestry of the Mulam ethnic group: admixture from ancient Yellow River, southern native, and Austronesian populations.

Human genetics·2026

Identification of novel loci regulating circulating melatonin and its causal relationship with hypertension.

Human genetics·2026

Severe arterial hypertension, a silent complication of Williams-Beuren syndrome: A case report with literature review.

Radiology case reports·2026

Cell-of-origin Discovery in Infant Leukemia through Integration of 3D Models and Patient Transcriptomic Data.

Journal of visualized experiments : JoVE·2026

Safety and Efficacy of Amotosalen-Ultraviolet A Pathogen-Reduced Platelets Transfused to Neonates.

Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie·2026

An unanticipated case of congenital high airway obstruction syndrome with type C tracheoesophageal fistula and cerebral ventriculomegaly in a preterm infant - is a small stomach a remote clue?

Case reports in perinatal medicine·2026

Role of Color Doppler and Microvascular Flow Imaging in the Assessment of Mesenteric Lymph Nodes in Pediatric Patients.

Cureus·2026

Impact of the neonatal intensive critical ultrasound workflow for managing neonatal acute pulmonary hypertension.

Frontiers in pediatrics·2026

Related Experiment Videos

Maternally transmitted extra ring (21) chromosome in a boy with Down's syndrome

Related Concept Videos

Factors secreted from dental pulp stem cells show multifaceted benefits for treating experimental temporomandibular joint osteoarthritis.

eNOS plays an important role in the regulation of colonic inflammation: a novel therapeutic target and a predictive marker for the prognosis of ulcerative colitis.

KRAS mutations in primary tumours and post-FOLFOX metastatic lesions in cases of colorectal cancer.

Effects of transglucosidase on diabetes, cardiovascular risk factors and hepatic biomarkers in patients with type 2 diabetes: a 12-week, randomized, double-blind, placebo-controlled trial.

KRAS mutations detected by the amplification refractory mutation system-Scorpion assays strongly correlate with therapeutic effect of cetuximab.

The effectiveness of packed therapy with three drugs in Helicobacter pylori eradication in Japan.

Clinical and zebrafish studies of truncating SF3B2-variants in craniofacial microsomia.

CRISPR/Cas9-based repair of a heterozygous HNF1A mutation in patient-derived hiPSCs.

TTC14 dysfunction contributing to microcephaly and lissencephaly spectrum features through protein mislocalization and impaired RNA processing.

The Russian FSHD registry: a first look at the cohort.

Genetic ancestry of the Mulam ethnic group: admixture from ancient Yellow River, southern native, and Austronesian populations.

Identification of novel loci regulating circulating melatonin and its causal relationship with hypertension.

Severe arterial hypertension, a silent complication of Williams-Beuren syndrome: A case report with literature review.

Cell-of-origin Discovery in Infant Leukemia through Integration of 3D Models and Patient Transcriptomic Data.

Safety and Efficacy of Amotosalen-Ultraviolet A Pathogen-Reduced Platelets Transfused to Neonates.

An unanticipated case of congenital high airway obstruction syndrome with type C tracheoesophageal fistula and cerebral ventriculomegaly in a preterm infant - is a small stomach a remote clue?

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Related Experiment Videos

Maternally transmitted extra ring (21) chromosome in a boy with Down's syndrome

Related Concept Videos

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