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A protein from fat-derived stem cells, DKK1, is linked to hair loss and blocking it may help treat alopecia areata.

Inherited color dilution in Rex rabbits is linked to DNA methylation changes in hair follicles.

DDR-II hair follicle cells don't respond to 1, 25-dihydroxyvitamin D3, aiding diagnosis.

A patient with a rare disease had a unique genetic mutation linked to their symptoms.

Daclizumab may cause psoriasis-like skin problems in multiple sclerosis patients.

Dermoscopy helped diagnose discoid lupus erythematosus in two patients without needing skin biopsies.

p63 controls Satb1 to help skin develop properly.

A person with a specific gene mutation had extra teeth, unique jaw and hair features not seen before in this condition.

Ectodysplasin-A1 is crucial for developing hair, teeth, and glands.

Overexpressing NSD3 in mice causes breast cancer-like tumors and gland abnormalities.

Tofacitinib effectively improved severe skin symptoms in a patient with Hypohidrotic Ectodermal Dysplasia.

Desmoglein 1 can partly make up for the loss of Desmoglein 3 in hair adhesion but not in mucous membranes.

SHISA6 helps maintain certain stem cells in mouse testes by blocking signals that would otherwise cause them to differentiate.

Hair microRNAs could be effective biomarkers for diagnosing scleroderma.

After skin is damaged, noncoding dsRNA helps prostaglandins and Wnts work together to repair tissue and promote hair growth.

Autoimmune Polyendocrine Syndromes involve specific combinations of autoimmune diseases.

Double stranded RNA helps skin wounds heal by coordinating specific proteins and signaling pathways.

Early diagnosis and treatment of discoid lupus erythematosus improve outcomes.

Mutations in the ABCB6 gene cause Dyschromatosis Universalis Hereditaria.

Interface dermatitis is the most common skin change in drug-induced hypersensitivity syndrome.

Early genetic testing and JAK inhibitors can help treat systemic inflammation in SAVI patients.

A peptide called DPS-1 helps human scalp cells grow and stimulates hair growth in mice.

Scalp hair follicle cells help protect and heal skin in certain skin conditions.

Dietary L-serine supplementation can reduce symptoms of HSAN1 by lowering harmful 1-deoxySL levels.

Aging changes female scalp cells, likely affecting hair health.

Longer TA repeats in the SRD5A2 gene may increase acne risk in Chinese people.

New mutations in the EBP gene cause CDPX2, affecting bones, skin, eyes, and hair, with females generally less affected than males.

A mutation in the Sgkl gene causes defective hair growth in mice.