Genetic analysis of Kawasaki syndrome

Novel Method to Target Apical Periodontitis Worsened by Inflammatory Bowel Disease.

Journal of dental research·2026

Securing the surgical field for mobilization of right-sided colon cancer using the duodenum-first multidirectional approach in laparoscopic surgery.

Techniques in coloproctology·2021

DNA hypermethylation of extracellular matrix-related genes in human periodontal fibroblasts induced by stimulation for a prolonged period with lipopolysaccharide derived from Porphyromonas gingivalis.

Journal of periodontal research·2015

Excess NF-κB induces ectopic odontogenesis in embryonic incisor epithelium.

Journal of dental research·2014

SLA-DRB1 and -DQB1 genotyping by the PCR-SSOP-Luminex method.

Tissue antigens·2011

Intra-bone marrow cotransplantation of donor mesenchymal stem cells in pig-to-NOD/SCID mouse bone marrow transplantation facilitates short-term xenogeneic hematopoietic engraftment.

Transplantation proceedings·2008

Exome analysis of 22,319 individuals links extremely rare copy-number variants and 22q11.21 dosage to Alzheimer risk.

American journal of human genetics·2026

Long-read transcriptome analysis using IsoRanker for identifying pathogenic variants in Mendelian conditions.

American journal of human genetics·2026

RNA splicing evidence enables robust classification of BRCA1 exon 18 variants: Results from the ENIGMA consortium.

American journal of human genetics·2026

Distinct mutational landscapes for germline and somatic cancer variants in forty tumor suppressor genes.

American journal of human genetics·2026

Shared genetic basis and structure of syndromic and normal facial variation.

American journal of human genetics·2026

The Gabriella Miller Kids First Data Resource for genomic research in pediatric cancer and congenital anomalies.

American journal of human genetics·2026

Genetic Testing for Neuromuscular Diseases.

Practical neurology (Fort Washington, Pa.)·2026

Expanding the Genotypic and Phenotypic Spectrum of Vissers-Bodmer Syndrome.

American journal of medical genetics. Part A·2026

Sequestration of CAPNS1 into Polyglycine Aggregates in a Cellular Model of NOTCH2NLC Repeat Expansion.

Biological & pharmaceutical bulletin·2026

Nephrogenic Syndrome of Inappropriate Antidiuresis: Case Report and Genetic Perspectives.

Nephrology (Carlton, Vic.)·2026

Unusual Variants in NDUFAF6-Associated Mitochondrial Disease.

Rare (Amsterdam, Netherlands)·2026

GRIN-related epilepsy in Chinese pediatric patients: a retrospective study of clinical, genetic, and mutant protein structural features in a tertiary center cohort.

World journal of pediatrics : WJP·2026

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Genetic analysis of Kawasaki syndrome

Related Concept Videos

Novel Method to Target Apical Periodontitis Worsened by Inflammatory Bowel Disease.

Securing the surgical field for mobilization of right-sided colon cancer using the duodenum-first multidirectional approach in laparoscopic surgery.

DNA hypermethylation of extracellular matrix-related genes in human periodontal fibroblasts induced by stimulation for a prolonged period with lipopolysaccharide derived from Porphyromonas gingivalis.

Excess NF-κB induces ectopic odontogenesis in embryonic incisor epithelium.

SLA-DRB1 and -DQB1 genotyping by the PCR-SSOP-Luminex method.

Intra-bone marrow cotransplantation of donor mesenchymal stem cells in pig-to-NOD/SCID mouse bone marrow transplantation facilitates short-term xenogeneic hematopoietic engraftment.

Exome analysis of 22,319 individuals links extremely rare copy-number variants and 22q11.21 dosage to Alzheimer risk.

Long-read transcriptome analysis using IsoRanker for identifying pathogenic variants in Mendelian conditions.

RNA splicing evidence enables robust classification of BRCA1 exon 18 variants: Results from the ENIGMA consortium.

Distinct mutational landscapes for germline and somatic cancer variants in forty tumor suppressor genes.

Shared genetic basis and structure of syndromic and normal facial variation.

The Gabriella Miller Kids First Data Resource for genomic research in pediatric cancer and congenital anomalies.

Genetic Testing for Neuromuscular Diseases.

Expanding the Genotypic and Phenotypic Spectrum of Vissers-Bodmer Syndrome.

Sequestration of CAPNS1 into Polyglycine Aggregates in a Cellular Model of NOTCH2NLC Repeat Expansion.

Nephrogenic Syndrome of Inappropriate Antidiuresis: Case Report and Genetic Perspectives.

Unusual Variants in NDUFAF6-Associated Mitochondrial Disease.

GRIN-related epilepsy in Chinese pediatric patients: a retrospective study of clinical, genetic, and mutant protein structural features in a tertiary center cohort.

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Genetic analysis of Kawasaki syndrome

Related Concept Videos

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