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Recent hair loss research shows some progress, especially in understanding male pattern baldness, but effective treatments for many types of hair loss are still lacking.

Most hair loss in children is caused by a few common conditions and is easy to diagnose, but rare types require careful evaluation.

The review shows how to properly diagnose and treat the loss of eyebrow and eyelash hair.

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

Maize hybrids show better early growth due to complex gene interactions from their parent strains.

The dog with an Alopecia Areata-like condition showed signs of an autoimmune disease and partially regrew hair without treatment, suggesting dogs could be models for human AA research.

The Wnt signaling pathway is not a major factor in the development of keratoacanthoma, a type of skin tumor.

Acne is a common skin condition linked to diet, hormones, and genetics, and early treatment can prevent scarring.

Molecular diagnostics help identify genetic defects causing endocrine diseases, improving diagnosis and treatment options.

Cats lose fur due to various reasons, including allergies, infections, genetics, hormones, diet, cancer, stress, and some conditions are treatable while others are not.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

The nucleus is key in controlling skin growth and repair by coordinating signals, gene regulators, and epigenetic changes.

Researchers discovered potential origins and new treatments for skin cancer, including biomarkers for melanoma and therapies that reduce tumor growth.

The document suggests a bacteria plays a significant role in acne rosacea and that white hair can regain color after transplant, meriting more research on reversing grey hair.

Understanding skin patterns can help us learn about skin diseases and their treatments.

Keratin proteins are crucial for hair structure and strength.

Hair ages due to genetics and environmental factors, leading to graying and thinning, with treatments available for some conditions.

Iron supplements may reverse premature graying in iron-deficient individuals; ingrown nails are common in diabetics with certain risk factors; topical finasteride may reduce scalp DHT as effectively as oral finasteride; monilethrix treatment is challenging but some medications can help.

Patients with ichthyosis often experience symptoms similar to psoriasis and atopic dermatitis, suggesting that targeted therapies could improve their condition.

Certain mouse strains develop a skin condition similar to a human hair loss disease due to genetic defects.

Understanding hair follicle biology and stem cell control could lead to new hair loss treatments.

Hair microscopy is useful for diagnosing certain hair loss conditions but has limitations and must be interpreted carefully.

The study created hair-bearing skin models that lack a key protein for skin layer attachment, limiting their use for certain skin disease research.

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

Fat-derived stem cells show promise for treating skin issues and improving wound healing, but more research is needed to confirm the best way to use them.

CCCA can affect both genders and all ages, and it has a genetic component.

Middle Eastern patients with epidermolysis bullosa show specific genetic mutations linked to different types of the disease.

Mutations in the Vitamin D receptor gene can cause hair loss similar to mutations in the Hairless gene.

TGM3 is important for skin and hair structure and may help diagnose cancer.

A patient with Birt-Hogg-Dubé Syndrome also had choroidal melanoma, suggesting the need for careful eyelid exams in such patients.