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A mutation in the vitamin D receptor causes severe resistance to vitamin D, affecting bone health but not hair growth.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

A specific gene change in APCDD1 increases the risk of hair loss.

Certain immune cells in atopic dermatitis skin could be targeted for treatment.

Higher activity in lichen planopilaris is linked to certain immune and tissue genes.

Certain gene variations increase male hair loss risk, influenced by hormone levels.

Lipid-antigen stimulation may play a role in folliculotropic mycosis fungoides.

Mutations in the hairless protein gene cause hair loss.

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.

Hair sensitivity to androgens is partly controlled by specific enzyme expressions in different hair areas.

PRDX5 enzyme may contribute to alopecia areata by affecting oxidative stress and autoimmunity.

Scientists found a new type of skin cell that could help with skin repair and these cells work better with a certain protein.

Certain genes influence immunoglobulin levels in Chinese Holstein cows, which can improve calf health.

CD1d expression in scalp skin and hair follicles changes with the hair cycle and may help protect against microbes.

Three characteristics of plasmacytoid dendritic cells help tell apart lupus-related hair loss from LPP.

Vitamin D receptor can control the hairless gene linked to hair loss even without vitamin D.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

A new IL6ST gene variant may cause a unique form of hyper-IgE syndrome with skin abscesses and high IgE levels.

Birt–Hogg–Dubé Syndrome requires genetic testing for accurate diagnosis due to its similarities with tuberous sclerosis.

Mutations in the AP1B1 gene cause a new syndrome with skin, hearing, and developmental issues.

Patients with Systemic Sclerosis have much higher levels of GDF-15, which could help predict organ involvement and guide treatment.

A 2-year-old girl with a rare vitamin D disorder had rickets and hair loss, but treatment was ineffective due to poor compliance.

A boy's growth and immune problems were caused by a new mutation in the STAT5B gene.

ILC1-like cells can cause alopecia areata by affecting hair follicles.

A specific genetic deletion in goats affects cashmere yield and thickness.

Certain gene variants can cause inherited hair diseases, which are important to diagnose and understand for patient care.

Nonimmunogenic forms of keratins K71 and K31 can delay and prevent alopecia areata.

LHX2 is essential for hair follicle development, controlled by NF-κB and TGFβ2 signaling.

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.