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Mast cells play a significant role in hair loss conditions like male pattern hair loss and alopecia areata.

The workshop highlighted the genetic links and psychological impacts of hair loss and skin disorders.

Female relatives of PCOS patients have a higher chance of showing PCOS symptoms.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

FGF13 gene changes cause excessive hair growth in a rare condition.

Alternating treatment with two drugs could help cells in a rapid aging disease.

AE can have varied symptoms and genetic causes, but zinc therapy helps.

Keratin protein production in cells is controlled by a complex system that changes with cell type, health, and conditions like injury or cancer.

High DHEA and short cervical length in women with PCOS and recurrent miscarriages may harm pregnancy outcomes.

mEphA1 receptor tyrosine kinase is important for skin and hair development and may play a role in certain diseases.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

Activating TERT in mice skin boosts hair growth by waking up hair follicle stem cells.

PCOS is a complex condition in women that can lead to health issues, and lifestyle changes are the best management approach.

Colorectal cancer development involves both genetic changes and epigenetic alterations like DNA methylation and microRNA changes.

Human skin cells have a high-affinity system for biotin transport, crucial for skin health.

Non-coding RNAs could help detect and treat radiation damage.

Mice without certain skin enzymes have faster hair growth and bigger eye glands.

A man with myotonic dystrophy type 1 had 28 skin cancers, suggesting a link between the disease and skin cancer, emphasizing the need for sun protection and regular skin checks.

An 11-year-old boy in Saudi Arabia has a rare case of hypoparathyroidism with severe brain calcifications but normal development and no known cause.

The 2024 guideline updates recommendations for genetic testing, imaging, and sperm retrieval in male infertility.

A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.

A girl with a rare genetic disorder had a unique bone condition, highlighting the need for careful diagnosis and suggesting the disorder might be more common than thought.

The JAK/STAT pathway is important in cell processes and disease, and JAK inhibitors are promising for treating related conditions.

Phosphorylation controls TFEB's location in the cell, affecting cell metabolism and stress response.

Alopecia areata is an autoimmune disease where T cells attack hair follicles.

More precise, personalized therapies are needed for autoimmune diseases.

FGF5 gene mutations cause unusually long eyelashes by affecting hair growth regulation.

Actinic keratosis can lead to skin cancer, is more common in fair-skinned people, and can be reduced with sunscreen and treated effectively.

Retinoic acid-binding proteins in skin are regulated by β-catenin and Notch signalling.

Progeroid mouse models show signs of early aging similar to humans, helping us understand aging better.