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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.

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.

Four patients with a type of rickets and hair loss had different mutations in their vitamin D receptor gene, causing it to not work properly.

A specific type of skin cell creates an opening for hair to grow out, and problems with this process can lead to skin conditions.

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.

New method finds genetic links between Type 2 Diabetes and Prostate Cancer not seen before.

Researchers created a mouse model of a type of rickets that does not cause hair loss.

Modified laparoscopic sleeve gastrectomy effectively controls diabetes and treats obesity with minimal complications.

A 15-year-old girl has a skin condition causing blisters on her feet, likely inherited from her family.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

miR-22, a type of microRNA, controls hair growth and its overproduction can cause hair loss, while its absence can speed up hair growth.

Hair and wool strength is affected by the number and type of bonds in their protein structures, with hair having more protein aggregates than wool.

The 675 nm laser effectively improved facial acne scars in dark skin with minimal side effects.