Absent right superior caval vein associated with partial trisomy 18

Heterotopia in microcephaly induced by cytosine arabinoside: hippocampus in the neocortex.

Acta neuropathologica·2000

Participation of calpain I activation in the ATP release reaction of platelets stimulated with thrombin.

Biochimica et biophysica acta·1992

Plasma calcitonin gene-related peptide levels in patients with various hypertensive diseases.

Journal of hypertension·1992

Deletion of mitochondrial DNA in the endomyocardial biopsy sample from a patient with Kearns-Sayre syndrome.

European heart journal·1992

[Clinical study of total parathyroidectomy and autotransplantation for secondary hyperparathyroidism].

Nihon Hinyokika Gakkai zasshi. The japanese journal of urology·1992

[Electrophysiologic study of cibenzoline in patients with paroxysmal atrial fibrillation with special reference to atrial fibrillation threshold].

Kokyu to junkan. Respiration & circulation·1992

miR-335-3p acts as a tumor suppressor in esophageal squamous cell carcinoma and predicts favorable prognosis.

Hereditas·2026

SNP rs7430456 mediated LINC00578 drives triple negative breast cancer through regulating miR-143-5p expression.

Hereditas·2026

BFLF1 gene polymorphisms are associated with increased mortality in patients with EBV-associated diseases.

Hereditas·2026

miR-1-3p, as a novel diagnostic and prognostic biomarker, aggravates pancreatic acinar cell injury in acute pancreatitis by targeting GNPTAB.

Hereditas·2026

Identification of FOXK1 and SEMA7A as key genes associated with m6A-related programmed cell death in diabetic retinopathy.

Hereditas·2026

miR-146b-5p serves as a novel biomarker for acute myocardial infarction and is involved in regulating oxidized low-density lipoprotein-induced endothelial injury through targeting PRKAR2A.

Hereditas·2026

Adult-Diagnosed Alagille Syndrome Presenting as Isolated Liver Disease.

Journal of clinical and experimental hepatology·2026

The Novel Allele, HLA-DPA1*01:213, With a Non-Synonymous Mutation in Exon 3.

HLA·2026

Adult subarachnoid hemorrhage from vein of Galen aneurysmal malformation due to ruptured feeder aneurysm: A case report with long-term MRI review.

Radiology case reports·2026

Novel Heterozygous Variant in RP1L1 Gene With Retinitis Pigmentosa Phenotype: A Case Report.

Ophthalmic surgery, lasers & imaging retina·2025

Large Infected Abdominal Wall Abscess Following a Minor Mechanical Strain: A Case Report.

Cureus·2025

[Main Trunk Interposition for Adult Anomalous Origin of the Left Coronary Artery from the Pulmonary Artery Using a Great Saphenous Vein:Report of a Case].

Kyobu geka. The Japanese journal of thoracic surgery·2025

Related Experiment Videos

Absent right superior caval vein associated with partial trisomy 18

Related Concept Videos

Heterotopia in microcephaly induced by cytosine arabinoside: hippocampus in the neocortex.

Participation of calpain I activation in the ATP release reaction of platelets stimulated with thrombin.

Plasma calcitonin gene-related peptide levels in patients with various hypertensive diseases.

Deletion of mitochondrial DNA in the endomyocardial biopsy sample from a patient with Kearns-Sayre syndrome.

[Clinical study of total parathyroidectomy and autotransplantation for secondary hyperparathyroidism].

[Electrophysiologic study of cibenzoline in patients with paroxysmal atrial fibrillation with special reference to atrial fibrillation threshold].

miR-335-3p acts as a tumor suppressor in esophageal squamous cell carcinoma and predicts favorable prognosis.

SNP rs7430456 mediated LINC00578 drives triple negative breast cancer through regulating miR-143-5p expression.

BFLF1 gene polymorphisms are associated with increased mortality in patients with EBV-associated diseases.

miR-1-3p, as a novel diagnostic and prognostic biomarker, aggravates pancreatic acinar cell injury in acute pancreatitis by targeting GNPTAB.

Identification of FOXK1 and SEMA7A as key genes associated with m6A-related programmed cell death in diabetic retinopathy.

miR-146b-5p serves as a novel biomarker for acute myocardial infarction and is involved in regulating oxidized low-density lipoprotein-induced endothelial injury through targeting PRKAR2A.

Adult-Diagnosed Alagille Syndrome Presenting as Isolated Liver Disease.

The Novel Allele, HLA-DPA1*01:213, With a Non-Synonymous Mutation in Exon 3.

Adult subarachnoid hemorrhage from vein of Galen aneurysmal malformation due to ruptured feeder aneurysm: A case report with long-term MRI review.

Novel Heterozygous Variant in RP1L1 Gene With Retinitis Pigmentosa Phenotype: A Case Report.

Large Infected Abdominal Wall Abscess Following a Minor Mechanical Strain: A Case Report.

[Main Trunk Interposition for Adult Anomalous Origin of the Left Coronary Artery from the Pulmonary Artery Using a Great Saphenous Vein:Report of a Case].

Related Experiment Videos

Absent right superior caval vein associated with partial trisomy 18

Related Concept Videos

Related Articles