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Different hair fiber development might explain why hair loss severity varies in patients with a specific genetic mutation, and treatments that thicken hair could help.

Hair microscopy is useful for diagnosing hair disorders, but clear definitions are needed for accurate genetic analysis.

Epigenetic factors play a crucial role in skin health and disease.

CRISPR/Cas9 has improved precision and control but still faces clinical challenges.

Drug repositioning offers hope for new, affordable treatments for a genetic skin disorder called ARCI.

Alopecia areata is an autoimmune condition causing hair loss, linked to genetic factors and immune system issues, with no cure yet.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

Hair loss in women often doesn't follow a pattern, isn't linked to age, may be genetic, and can be related to thyroid issues or other health factors.

Patients with myotonic dystrophy often have skin problems that suggest early aging and vitamin D issues, and the severity of these problems is linked to their genetic condition and vitamin D levels.

Dermatologists give better information on pathology forms, hypersensitivity vasculitis is a common skin issue, misdiagnoses can occur, and various skin conditions are linked to loss of elastin or genetic factors.

Ichthyoses are genetic skin disorders that affect the skin's barrier function.

The essay suggests hair loss might be caused by changes in skull bones.

The book is a valuable guide for hair restoration surgeons.

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

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

Genetic variations in hair keratin proteins exist but don't significantly affect hair structure.

Genetic defects in androgen production are linked to male developmental disorders and are improving treatment understanding.

Drug repositioning is becoming more targeted and efficient with new technologies, offering personalized treatment options and growing interest in the field.

Eruptive vellus hair cysts are a cosmetic skin condition, more common in young adults, with few effective treatments.

Abnormal scalp whorls can indicate brain development issues but may also be seen in neurologically normal people.

The document concludes that lifestyle changes and medical treatments can significantly reduce symptoms of Hidradenitis Suppurativa, a chronic skin condition.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

Frontal Fibrosing Alopecia is a poorly understood condition that is hard to treat and causes distressing hair loss.

Genetic research may lead to better ways to predict and treat male-pattern hair loss.

Certain genetic mutations can lower bad cholesterol and reduce heart disease risk, leading to effective cholesterol-lowering drugs.

The Rotterdam Study updated findings on elderly health, focusing on heart disease, genetics, lifestyle effects, and disease understanding.

Stem cell niches are crucial for regulating stem cell behavior and tissue health, and their decline can impact aging and cancer.

The Rotterdam Study updated its design and objectives in 2012, providing insights into various diseases in the elderly, including skin cancer, bone health, liver disease, neurological and psychiatric conditions, and respiratory issues.

Biomaterials with MSC-derived substances could improve tissue repair and have advantages over direct cell therapy.

Shorter CAG repeats may cause hair and skin issues, while longer ones may link to acne.