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Hairless protein is crucial for healthy skin and hair, and its malfunction can cause hair loss.

Gata6 is important for protecting hair growth cells from DNA damage and keeping normal hair growth.

Hair disorders are caused by a complex mix of biology, genetics, hormones, and environmental factors, affecting hair growth and leading to conditions like alopecia.

Hair loss involves immune responses, inflammation, and disrupted signaling pathways.

Cholesterol balance is important for hair health, and problems with it can lead to hair loss conditions.

The document concludes that accurate diagnosis of hair loss in children is crucial due to limited treatment options and the condition's psychological impact.

The review concludes that accurate diagnosis of different types of hair loss requires proper biopsy techniques and understanding the hair growth cycle and underlying causes.

Researchers identified specific genes that are important for mouse skin cell development and healing.

A boy had unusual synchronized hair growth with short active growth phases, not fitting known hair disorders.

Hair microscopy is useful for diagnosing certain hair loss conditions but has limitations and must be interpreted carefully.

Vitamin D receptor helps control hair growth genes in skin cells.

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

The study found genetic differences related to hair development that may explain hair loss in a patient with Trichorhinophalangeal syndrome type I.

PTHRP agonists can stimulate hair growth, especially in damaged follicles, while antagonists may initially increase growth but ultimately inhibit it.

Certain genes are more active in baby scalp cells and can help grow hair when added to adult mouse skin cells.

Early diagnosis and treatment, like topical minoxidil, can prevent hair loss in children.

A spermidine-based supplement may help hair grow longer by keeping it in the growth phase.

Key genes linked to hair growth and cancer were identified in hairless mice.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

The document concludes that periocular hair disorders have various causes and treatments, and proper evaluation by specialists is important for management and prognosis.

The Hairless gene is crucial for hair cell development, affecting whether skin cells become hair or skin and oil gland cells.

The commentary explains that a balance of HR protein and putrescine is important for normal hair growth.

The document concludes that early diagnosis and a comprehensive treatment plan are crucial for managing hair loss in children, with a focus on both medical and psychological support.

Certain genes controlled by OVOL1 are crucial for creating new hair follicles.

The unique coat of lykoi cats is likely caused by new variants in the Hairless gene.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

Photodynamic therapy may not work for erythroplasia of Queyrat and could lead to invasive squamous cell carcinoma.

Telogen Effluvium is a common hair loss condition, particularly in women, with no specific FDA-approved treatment, and recovery can take up to 18 months.

Telogen Effluvium is a common hair loss condition that can be short-term or long-lasting and is often caused by stress, illness, or nutritional issues.

Diagnosing alopecia areata is challenging and requires careful examination and various tests to distinguish it from other hair loss types.