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The conference presented findings on how vitamin D levels, genetic factors, and lifestyle choices like smoking and yoga affect various health conditions and diseases.

The scraggly mutation causes hair loss and skin defects in mice.

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

Human hair follicle cells can be turned into stem cells that may help clone hair for treating hair loss or burns.

Edar signaling is crucial for controlling hair growth and regression.

Longer CAG and GGN repeats increase alopecia risk, but no significant link to post-finasteride syndrome found.

Certain genes are linked to the risk of developing Alopecia Areata.

Researchers found a safe and effective way to pick genetically modified skin cells with high growth potential using CD24.

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

Hair loss may indicate a higher risk of heart disease and other health issues related to metabolism.

New methods have greatly improved our understanding of stem cell behavior and roles in the body.

Men may have a condition similar to PCOS, possibly indicated by early hair loss.

Genetics, low estrogen, and low iron levels contribute to female hair loss, with specific scalp signs indicating severity.

The cause of Frontal Fibrosing Alopecia is unclear, diagnosis involves clinical evaluation and various treatments exist, but their effectiveness is uncertain.

Wnt proteins from certain skin cells are crucial for normal hair growth and renewal.

Plucked hairs can be used instead of skin biopsies to study hair traits because they contain specific cells related to hair.

Mutations in specific llama genes may affect fiber quality for textiles.

Human Schwann cells can be quickly made from hair follicle stem cells for nerve repair.

The research found genes that change during cashmere goat hair growth and could help determine the best time to harvest cashmere.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

Higher miR-34a levels and the A variant of the MIR-34A gene are linked to increased risk and severity of alopecia areata.

The document concludes that there have been significant improvements in diagnosing and treating skin diseases, including melanoma, with new techniques and therapies.

Different hair follicles in the skin are innervated by unique combinations of mechanosensory neurons, crucial for touch sensation.

The document concludes that hirsutism is the main sign for diagnosing hyperandrogenism, which requires a detailed patient history and physical exam.

EDA2R gene linked to hair loss.

Noggin overexpression delays eyelid opening by affecting cell death and skin cell development.

The document concludes that early and personalized treatment for PCOS in adolescents is crucial to manage symptoms and prevent long-term health issues.

The KRTAP21-2 gene affects wool length and quality in sheep.

The document concludes that various findings in rheumatology offer insights into disease severity, treatment responses, and potential risks in medication, with some limitations due to unspecified participant numbers.

The review shows that skin symptoms like chronic fungal infections, hair loss, and skin depigmentation are key for early detection and management of APECED.