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The nude gene causes skin cell overgrowth and improper development, leading to hair and urinary issues.

PEGylated liposomal doxorubicin improves cancer treatment effectiveness and reduces side effects like heart damage and hair loss.

Common hair loss disorders may not need stem cell therapy, but could benefit from other treatments like hair cycle control and immune restoration therapy.

Eating glucoraphanin can help prevent psychosis in offspring whose mothers had immune system activation.

Hair loss in women is genetic, diagnosed by examination and biopsy, and treated with minoxidil, finasteride, or transplantation.

The meeting covered advances in understanding hair growth, causes of hair loss, and potential treatments.

HSD11b1 affects skin nerves and increases non-histaminergic itch.

A woman with Kallman's syndrome also developed alopecia universalis, a condition not previously linked to Kallman's.

The vitamin D receptor can act without its usual activating molecule, affecting hair growth and skin cancer, but its full range of actions is not well understood.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

High androgen levels can cause excessive hair growth and may indicate serious health issues, including heart disease and fertility problems.

The document reviews various hair and nail disorders, their causes, and treatments, emphasizing the need for proper diagnosis and the link between nail changes and systemic diseases.

Long-haul COVID can cause lasting symptoms affecting many body systems and may be linked to ongoing inflammation and immune system issues.

Excessive hair growth in women often has no known cause and is not linked to race or other hormonal symptoms.

Vitamin D Receptor is crucial for hair follicle shrinkage and cell death, affecting hair growth.

Vitamin D and its receptor regulate skin functions like cell growth, immunity, hair cycle, and tumor prevention.

Hair thinning and loss in a girl with a rare metabolic disorder was linked to her condition.

Defects in certain proteins cause major heart abnormalities during early development.

Mice lacking Insig proteins had hair growth problems due to cholesterol buildup, but this was fixed by the drug simvastatin.

Laminin 332 is essential for normal skin cell behavior and structure.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

Thymoma in cats can cause hair loss without inflammation.

Adult mice with CBS deficiency show minimal health issues and normal lifespan despite high homocysteine levels.

PPAR-γ is important for healthy hair and its problems, and more research on PPAR-γ treatments is needed.

Melanocyte stem cells are crucial for skin pigmentation and have potential in disease modeling and regenerative medicine.

Ayurvedic treatment, exercise, and a healthy diet can effectively manage PCOD symptoms.

Different types of cell death affect skin health and inflammation, and understanding them could improve treatments for skin diseases.

Different sPLA2 enzymes affect immunity, skin and hair health, reproduction, and may be potential targets for therapy.

Hair loss can be linked to hormonal changes, and physical conditions like heart defects can cause depression.