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Proteins like aPKC and PDGF-AA, substances like adenosine and ATP, and adipose-derived stem cells all play important roles in hair growth and health, and could potentially be used to treat hair loss and skin conditions.

Found new possible treatments for hair loss.

New genetic locations explain much of hair color variation in Europeans.

Melanocytes are crucial for skin pigmentation and can affect conditions like melanoma, vitiligo, and albinism, as well as hair color and hearing.

Hidradenitis suppurativa is caused by genetic factors, inflammation, bacteria, hormones, and lifestyle factors like obesity and smoking.

Noggin gene inactivation causes skeletal defects in mice, varying by genetic background.

Accurate clinical, histological, and genetic methods are key for understanding and treating hair disorders.

Future research on ectodysplasin should explore its role in diseases, stem cells, and evolution, and continue developing treatments for genetic disorders like hypohidrotic ectodermal dysplasia.

Researchers created a mouse model of a type of rickets that does not cause hair loss.

The document concludes that ongoing research using animal models is crucial for better understanding and treating Alopecia Areata.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

No clear link between androgen receptor variation and hair loss, but more research needed.

Combining skin tissue pathology with genetics has greatly improved the diagnosis and understanding of certain skin diseases.

Foxn1 gene regulation is crucial for thymus development but not for hair growth.

The circadian clock in skin cells controls their growth and rest cycles.

Bald thigh syndrome in sighthounds is caused by structural defects in hair shafts due to downregulated genes and proteins.

Crossbreeding improves goat fiber quality, and specific genes affect hair traits and color.

Mechanical forces are crucial for shaping cells and forming tissues during development.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

The research found a way to identify and study skin cells with stem cell traits, revealing they behave differently in culture and questioning current stemness assessment methods.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

The conclusion suggests that prostate cancer should be classified by castration status and that new therapies targeting androgen receptor signaling show promise.

Understanding how epigenetic regulation affects stem cells is key to cancer insights and new treatments.

UVA1-light therapy successfully treated a child's skin condition, mycosis fungoides.

New technologies help us better understand how skin microbes affect skin diseases.

Hidradenitis Suppurativa is a chronic skin condition best treated early with surgery for better outcomes and less recurrence.

Terbinafine is the most effective treatment for tinea capitis, a scalp infection often confused with other conditions.

Scientists made a mouse that shows how a specific protein in the skin changes and affects hair growth and shape.

Two main types of fibroblasts with unique functions and additional subtypes were identified in human skin.

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