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Recent findings suggest that genetic factors, immune system issues, and skin cell defects might contribute to the development of hidradenitis suppurativa.

The research linked PLCD1 gene variants to the development of trichilemmal cysts.

Genetic mutations that disrupt homocysteine breakdown lead to increased damage in mouse hair keratin.

Trichoscopy is a useful tool for diagnosing hair and scalp diseases without needing skin biopsies.

Doctors need to understand statistics to properly evaluate clinical trials for patient care.

The review highlights the importance of stem cells in hair health and suggests new treatment strategies for hair loss conditions.

Prunus mira Koehne is valuable for hair growth and has potential for sustainable use, but needs more research and conservation.

Scalp basal cell carcinoma may be more aggressive and harder to treat than other types, requiring special attention and further research.

Wire brush snares are best for collecting Eurasian Lynx hair for DNA analysis.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

Improving knowledge and practices in animal fibre production is crucial to meet market demands and potentially revive natural fibres.

Oxidative stress may contribute to hair loss in alopecia areata and antioxidants could potentially help as a treatment.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

Genetic testing is crucial before giving azathioprine to avoid severe side effects.

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.

Animal models, especially mice, are essential for advancing hair loss research and treatment.

A man with testotoxicosis was fertile despite low FSH levels, suggesting high testosterone may allow sperm production without FSH.

Early diagnosis and treatment of Hidradenitis Suppurativa are important to prevent serious physical and mental effects.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

Some women with PCOS have rare genetic variants linked to the condition.

Epidermal stem cells show promise for future dermatology treatments due to ongoing advancements.

Hair quality is genetically determined and linked to its composition and strength.

Mutation in hairless gene may increase hair loss risk.

Genetic screening for NUDT15 polymorphisms is crucial for patients taking azathioprine, especially in Asians.

Male and female hair loss have different genetic causes.

Heredity and hormones cause common hair loss, and topical minoxidil is the first recommended treatment.

Hidradenitis suppurativa is a chronic skin condition more common in women, linked to genetics and lifestyle factors, and associated with various other health issues.

Most drugs fail to reach the market, but understanding their properties and using strategies like early toxicity tests and drug repurposing can help advance their development.

UV photography can help identify people at higher risk for skin cancer, and male pattern baldness at age 45 is linked to a higher risk of certain skin cancers.

Advancements in hair follicle culture have led to better understanding and potential treatments for hair loss.