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TFC-loaded microneedles effectively promote hair regrowth in androgenetic alopecia.

The rs231775 genetic variant is linked to a higher risk and severity of Alopecia Areata in males.

An 11-year-old girl with Trichotillomania developed a large hairball in her stomach, treated with medication, therapy, and family education.

Trichodysplasia spinulosa is a rare skin condition caused by a virus, treatable with antiviral medication.

Patients with the same genetic mutation for vitamin D-resistant rickets showed different symptoms but all improved with treatment except for hair loss.

New mutations in KRT83 and KRT86 are linked to the hair disorder monilethrix.

A new CDH3 gene mutation was found in a Spanish patient with sparse hair and eye issues.

The gene Tfap2b is essential for creating a type of stem cell in zebrafish that can become different pigment cells.

The TG5 gene affects beef cattle weight, and the CC genotype leads to higher weights.

Two siblings have a rare hair condition caused by a new genetic variant.

A new therapy for a skin blistering condition has not been developed yet.

Targeting Vδ1+T-cells may help treat alopecia areata.

Adults with Beta Thalassemia Major are more likely to have skin, hair, and nail disorders.

Dacomitinib can cause nail and skin issues, but these can be managed without stopping the drug.

High glycine–tyrosine keratin-associated proteins help make hair strong and maintain its shape.

Trastuzumab may cause tufted hair folliculitis as a side effect.

FOXN1 mutations cause severe immunodeficiency, hair loss, nail issues, and thymus defects.

Some drugs for inflammation may cause psoriasis-like hair loss.

The role of γδT-cells in causing alopecia areata remains unclear.

A49T gene variant linked to higher prostate cancer risk, lower hormone levels, and slightly reduced balding risk.

Thioredoxin reductase 1 does not affect glucocorticoid receptor activity in hair follicle cells.

Long-standing benign tumors can become cancerous, especially in people with weakened immune systems.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

Plet-1 protein helps hair follicle cells move and stick to tissues.

The study concludes that a genetic mutation in TFM mice leads to reduced androgen receptor activity, affecting the body's response to male hormones.

TNF alpha in skin cells causes weight loss, hair and fat issues, and skin inflammation in mice.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.