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The study found genetic differences related to hair development that may explain hair loss in a patient with Trichorhinophalangeal syndrome type I.

Keratin 33A is a key protein in goat winter coats, especially in high-producing breeds.

A woman had a delayed allergic reaction to the blood thinner enoxaparin, treated with a steroid cream.

Tailored nonsurgical cosmetic procedures are crucial for safely treating diverse skin types, especially skin of color.

Finasteride's polymorphic form affects capsule quality and drug effect, requiring strict control.

Alcoholic solvent improves selectivity in key intermediate for finasteride and dutasteride synthesis.

Finasteride metabolites found in pigs match human studies, making pigs a valid model for human drug research.

Early diagnosis and treatment are crucial for preventing permanent hair loss in various scalp conditions, and while new treatments are promising, more research is needed to evaluate their effectiveness.

Some congenital hair disorders improve with age and can be managed with treatments like minoxidil, retinoids, supplements, and gentle hair care, but there's no cure.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

Type 2 diabetes slows down skin and hair renewal by blocking important stem cell activation in mice.

PAD3 plays a key role in hair and skin protein structure and may be linked to skin diseases.

Women with PCOS are more likely to have insulin resistance and obesity, especially those with the most severe type I PCOS.

Type I interferons play a key role in the development of various skin diseases.

A fragment of human type XVII collagen shows great potential for skin health and wound healing.

Chinese men have lower AGA rates than Caucasians, with type III vertex most common; family history is important.

PRP combined with minoxidil is the most effective and safe treatment for male pattern baldness.

AGA increased yearly, type I most common, and family history and seborrheic dermatitis often linked.

The study created a model to help design new inhibitors for steroidal 5α-reductase enzymes.

Type 1 diabetes often occurs with other autoimmune diseases, and personalized treatment based on genetics can improve outcomes.

Leptin-deficient mice, used as a model for Type 2 Diabetes, have delayed wound healing due to impaired contraction and other dysfunctional cellular responses.

Indian men have 62.1% hair loss, mostly grade II vertex, and less extensive than other populations.

Type 3 Innate Lymphoid Cells help maintain skin health and balance, and are involved in skin diseases and healing.

A type of collagen helps hair grow by boosting cell growth and activating a specific hair growth pathway.

Insulin resistance increases the risk of developing type 2 diabetes and other health issues.

Ishige sinicola, a type of seaweed, may help hair grow by blocking a hair loss-related enzyme and boosting important cell growth.

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

A rare genetic disease causes rickets and often hair loss in young children, which can improve with specific treatments.

Two siblings with a rare type of rickets and hair loss had low vitamin D levels, which is not typical for their condition.

Alopecia areata is a type of hair loss that can lead to complete baldness, often associated with other autoimmune conditions, and half of the cases may see hair return within a year.