Infantile liver hemangiomatosis: evidence for molecular heterogeneity

Influence of intrinsic noise generated by a thermotesting device on thermal sensory detection and thermal pain detection thresholds.

Muscle & nerve·2009

Neonatal-onset multisystem inflammatory disease (NOMID) due to a novel S331R mutation of the CIAS1 gene and response to interleukin-1 receptor antagonist treatment.

American journal of medical genetics. Part A·2006

The homeobox transcription factor Prox1 is highly conserved in embryonic hepatoblasts and in adult and transformed hepatocytes, but is absent from bile duct epithelium.

Anatomy and embryology·2004

Microarray-analysis: a new approach to study the molecular mechanisms of thermo-chemotherapy.

Klinische Padiatrie·2003

Proteomics: techniques and applications in cancer research.

Klinische Padiatrie·2003

High-dose chemotherapy with autologous stem cell rescue in children with retinoblastoma.

Bone marrow transplantation·2003

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The Journal of pediatrics·2026

Associations Between Saliva-Based Biomarkers and Pediatric Concussion Subtypes.

The Journal of pediatrics·2026

Outpatient Respiratory Outcomes in Infants Who Survive Hospitalization for Extreme Prematurity.

The Journal of pediatrics·2026

Relationship Between Bronchopulmonary Dysplasia, Corpus Callosum Microstructure at Term-Equivalent Age, and Neurodevelopment at Age 2 Years in Infants Born Preterm.

The Journal of pediatrics·2026

Magnetic Resonance Imaging During Therapeutic Hypothermia Accurately Reflects the Degree of Brain Injury in Neonates with Hypoxic-Ischemic Encephalopathy.

The Journal of pediatrics·2026

Acute Emotional Symptoms Predict Emotional Functioning Up to 6 Months After Pediatric Concussion: An A-CAP Study.

The Journal of pediatrics·2026

Genetic variant profile in a cohort of inherited bone marrow failure patients from North india.

Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion·2026

Appreciating diversity: a review of the Iranian genomic landscape.

European journal of human genetics : EJHG·2026

The role of ferroptosis in juvenile idiopathic arthritis: Causal inference and mediation by immune phenotypes.

Medicine·2026

Generation and characterization of an isogenic gene-corrected iPSC line CARIMi009-A-1 from a Hutchinson-Gilford Progeria Syndrome (HGPS) patient with a heterozygous G608G mutation in the LMNA gene.

Stem cell research·2026

A Rare De Novo Missense Mutation in IFT122 Confers a Genetic Susceptibility Factor of Idiopathic Pediatric Uveitis Via Trio-based Whole-Exome Sequencing.

Advanced science (Weinheim, Baden-Wurttemberg, Germany)·2026

Integrated Genomic and Proteomic Analysis Reveals T-B Lymphocyte Signatures in the MYCN Driven "Immune Desert" of Specific Neuroblastoma Subtypes.

CNS neuroscience & therapeutics·2026

Related Experiment Videos

Infantile liver hemangiomatosis: evidence for molecular heterogeneity

Related Concept Videos

Influence of intrinsic noise generated by a thermotesting device on thermal sensory detection and thermal pain detection thresholds.

Neonatal-onset multisystem inflammatory disease (NOMID) due to a novel S331R mutation of the CIAS1 gene and response to interleukin-1 receptor antagonist treatment.

The homeobox transcription factor Prox1 is highly conserved in embryonic hepatoblasts and in adult and transformed hepatocytes, but is absent from bile duct epithelium.

Microarray-analysis: a new approach to study the molecular mechanisms of thermo-chemotherapy.

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School-Based Health and Healthcare Utilization Among Rural Youth: Evidence from a School-Based Health Center Opening.

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Genetic variant profile in a cohort of inherited bone marrow failure patients from North india.

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Generation and characterization of an isogenic gene-corrected iPSC line CARIMi009-A-1 from a Hutchinson-Gilford Progeria Syndrome (HGPS) patient with a heterozygous G608G mutation in the LMNA gene.

A Rare De Novo Missense Mutation in IFT122 Confers a Genetic Susceptibility Factor of Idiopathic Pediatric Uveitis Via Trio-based Whole-Exome Sequencing.

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Infantile liver hemangiomatosis: evidence for molecular heterogeneity

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