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Researchers found new hair and nail genes, how hair reacts to UV, differences in white and pigmented hair growth, nerve changes in alopecia, treatments for baldness and alopecia, a toenail condition linked to a genetic disorder, and that nail fungus is more common in people with psoriasis.

A 3-month stay in space causes skin thinning, disrupts hair growth, and changes muscle-related genes in mice.

Two teenage brothers had a rare, treatment-resistant form of female-pattern hair loss with unusual scalp changes.

Lichen Planus is a less common condition affecting skin and mucous membranes, with various types and associated risk factors, challenging to diagnose, significantly impacts life quality, and may have a risk of cancerous changes in oral lesions.

The guide explains how to identify and treat children's hair loss, including fungal infections, autoimmune disorders, hairstyle changes, self-correcting conditions, and behavioral therapy for hair-pulling.

A 17-year-old developed woolly hair nevus in adolescence, which is unusual, and over time the hair darkened and straightened slightly, but microscopic changes persisted.

The nucleus is key in controlling skin growth and repair by coordinating signals, gene regulators, and epigenetic changes.

New mutations in hair keratin genes can change hair structure and cause monilethrix, with nail issues more common in certain gene mutations.

Hormonal changes and social stress may link lupus and eating disorders in teens.

Genetic changes in specific proteins contribute to hair loss in some women of African descent.

Skin changes are key for early diagnosis and treatment of rheumatic diseases.

Skin color may change how alopecia areata looks under a dermoscope.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

Microarray analysis helps find hidden chromosomal changes in patients with intellectual disabilities and birth defects.

CD44 variant changes start alopecia areata, but don't maintain it.

Certain genetic changes in the KRT82 gene may cause patchy skin in New Zealand rabbits.

Fibroblasts from healthy donors can prevent changes seen in recessive epidermolysis bullosa simplex.

Loose anagen hair syndrome is caused by structural abnormalities in the hair follicle's inner root sheath.

Public interest in skin issues changed during COVID-19, with more focus on dry skin, hair problems, and hand eczema.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Capsaicin cream quickly relieved itching in two patients with brachioradial pruritus.

Dermal adipose tissue in mice can change and revert to help with skin health.

Telocytes help organize male reproductive tissues and their changes can lead to diseases.

Skin and mucous membrane issues are common in kids after bone marrow transplants, so careful monitoring is crucial.

Hypothyroidism-related skin issues in dogs are most common in older male Labradors, causing hair loss, slow heart rate, and obesity.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

A woman's heart failure improved after she added vitamins and changed her diet from only cheese chips and cake.

Chemotherapy damages hair follicles, causing hair loss and other cellular changes.