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New compounds effective against SARS-CoV-2 variants were identified using a rapid testing method with human lung cells.

Oral contraceptive use may increase the risk of frontal fibrosing alopecia in women with a specific CYP1B1 gene variant.

Continued vaccine and drug development is crucial due to new virus variants and regional infection spikes.

Genetic factors, especially PADI3 gene variants, contribute to CCCA in women of African descent.

Long-COVID symptoms in children after MIS-C are similar across different COVID-19 variants, with older age being a key factor.

A young man with an unusual type of scarring hair loss suggests a possible new variant of a known scalp condition.

Myhre syndrome symptoms worsen over time, with specific genetic variants affecting severity.

The KRTAP19-5 gene affects wool curvature in Chinese Tan sheep, with Variant B reducing curvature.

Most people have similar hair protein patterns, but a rare variant was found in two women.

Most people with post-COVID syndrome experience symptoms like fatigue, but Omicron variants cause fewer persistent symptoms.

Lower adrenal hormone levels may cause hair loss in postmenopausal women, certain patterns help diagnose nail cancer, and a gene variant linked to higher skin cancer risk in kidney transplant patients suggests monitoring folate levels.

Changing the pin and cupola setup reduced hair loss in Orthodox Jews using skull-caps.

Silencing NtNCED3-2 gene in tobacco reduces drought tolerance and impairs growth.

Follicular mucinosis can be an early sign of aggressive mycosis fungoides.

Targeting ACE2 and TMPRSS2 may help prevent or treat COVID-19 in cancer patients.

The cyst had unusual keratin spherules and resembled bone marrow.

A mutation in the EDNRA gene causes Oro-Oto-Cardiac syndrome, affecting face and heart development.

A unique type of hair loss mimics another condition but has minimal inflammation and specific immune cells present.

Folliculotropic Mycosis Fungoides requires stage-based treatment, with early stages using skin therapies and advanced stages needing aggressive treatments.

People with keratosis pilaris might be more likely to get a rare type of tinea versicolor.

Folliculotropic mycosis fungoides has a worse prognosis than other types, with survival rates varying significantly based on subtype and organ involvement.

Gene and cell therapies are being developed to treat rare skin conditions like epidermolysis bullosa and ichthyosis.

The KAP 7 gene affects wool traits in Rambouillet sheep, with the BB genotype showing the best wool characteristics.

Keratin K80 is an ancient protein found in various tissues, important for cell structure and tissue differentiation.

Basal cell carcinoma with matrical differentiation is a rare type linked to hair follicles, with .-catenin important for its development.

Linear lichen planopilaris can affect the trunk, not just the face.

A 6-year-old boy's skin condition improved after stopping a specific treatment and starting new medications.

A stable, active version of a growth factor was made in bacteria, showing promise for medical use.

GLPLS is a rare skin condition with specific hair loss and skin symptoms.

Flexural follicular lichen planus is a rare skin condition affecting body folds.