Genetic analysis of 21-hydroxylase deficiency--possible role of gene conversion in monogenic disease

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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

Effects of HLA-DPB1 genotypes on chronic hepatitis B infection in Japanese individuals.

Tissue antigens·2015

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

Journal of dental research·2014

Associations of HLA class I alleles in Japanese patients with Crohn's disease.

Genes and immunity·2014

An update to HLA nomenclature, 2010.

Bone marrow transplantation·2010

Pocket Monster incident and low luminance visual stimuli: special reference to deep red flicker stimulation.

Acta paediatrica Japonica : Overseas edition·1999

Photosensitive fits elicited by TV animation: an electroencephalographic study.

Acta paediatrica Japonica : Overseas edition·1999

Subclinical Sjögren's syndrome: a significant 67gallium accumulation in the orbits and parotid glands.

Acta paediatrica Japonica : Overseas edition·1999

Trisomy 6 in a childhood acute mixed lineage leukemia.

Acta paediatrica Japonica : Overseas edition·1999

Hereditary pancreatitis: report of a family from Turkey.

Acta paediatrica Japonica : Overseas edition·1999

An infant with Costello syndrome complicated with fatal hypertrophic obstructive cardiomyopathy.

Acta paediatrica Japonica : Overseas edition·1999

Temporal and bidirectional associations of sleep-wake behavior in adolescentes.

Chronobiology international·2026

DGAT1, but Not DGAT2, Is Required for Ovarian Lipid Storage and Egg Hatchability in Rhodnius prolixus.

Insect biochemistry and molecular biology·2026

The limits of genetic screening: trisomy 21 after euploid preimplantation genetic testing for aneuploidy and negative noninvasive prenatal testing.

F&S reports·2026

Correlation of whole-body fat content and its distribution with lumbar fat content under different age, gender and BMI conditions: quantitative analysis of MRI based on deep learning.

BMC musculoskeletal disorders·2026

Early lineage divergence segregates sensory and motor-associative identities in the thalamus.

Nature neuroscience·2026

Familial 46,XX Ovotesticular Differences in Sex Development Associated With an NR5A1 p.Arg92Trp Variant.

Hormone research in paediatrics·2026

Related Experiment Videos

Genetic analysis of 21-hydroxylase deficiency--possible role of gene conversion in monogenic disease

Related Concept Videos

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

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

Effects of HLA-DPB1 genotypes on chronic hepatitis B infection in Japanese individuals.

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

Associations of HLA class I alleles in Japanese patients with Crohn's disease.

An update to HLA nomenclature, 2010.

Pocket Monster incident and low luminance visual stimuli: special reference to deep red flicker stimulation.

Photosensitive fits elicited by TV animation: an electroencephalographic study.

Subclinical Sjögren's syndrome: a significant 67gallium accumulation in the orbits and parotid glands.

Trisomy 6 in a childhood acute mixed lineage leukemia.

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An infant with Costello syndrome complicated with fatal hypertrophic obstructive cardiomyopathy.

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DGAT1, but Not DGAT2, Is Required for Ovarian Lipid Storage and Egg Hatchability in Rhodnius prolixus.

The limits of genetic screening: trisomy 21 after euploid preimplantation genetic testing for aneuploidy and negative noninvasive prenatal testing.

Correlation of whole-body fat content and its distribution with lumbar fat content under different age, gender and BMI conditions: quantitative analysis of MRI based on deep learning.

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Genetic analysis of 21-hydroxylase deficiency--possible role of gene conversion in monogenic disease

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