Search

everythinglearnresearchcommunity

for

Search:↓

The human scalp hair bulb contains different types of melanocytes with varying abilities to produce melanin.

Hair microscopy is a simple and cost-effective method to help diagnose systemic diseases in children.

Boreal caribou in northeastern British Columbia have significant health issues, including infections, tick infestations, and mineral deficiencies.

More research is needed to understand how testosterone is maintained in adult males.

Understanding fetal skin development helps diagnose congenital skin diseases.

Over half of the dog skin disorders discussed have known gene variants, enabling genetic testing for diagnosis and responsible breeding.

New genetic mutations linked to rare skin disorders were found in three newborns.

A child with skin and heart issues had rare genetic mutations affecting skin and heart cell cohesion.

Skin symptoms are important for diagnosing infections in children.

Three related Persian cats have a rare, likely hereditary skin condition causing hair loss and poor coat quality, with limited treatment options.

Cholesterol balance is important for hair health, and problems with it can lead to hair loss conditions.

A specific gene mutation causes Olmsted syndrome.

Crossbreeding certain European cattle breeds may cause hair and physical issues in cattle.

Skin grafting is a key procedure for repairing skin defects, with the success depending on the right graft choice, donor site management, and aftercare.

Some babies are born with alopecia areata, and a treatment with clobetasol propionate can regrow hair in half of the cases.

Immune cells are essential for early hair and skin development and healing.

Using skin grafts from behind the ear for oral surgery in two patients with jaw injuries led to successful healing and good results.

Skin grafts are effective for chronic leg ulcers, especially autologous split-thickness grafts for venous ulcers, but more data is needed for diabetic ulcers.

Sebaceous glands play a key role in skin health, immunity, and various skin diseases.

Low-potency steroids can cause serious side effects in people with skin conditions like Netherton syndrome.

Inherited ichthyoses cause widespread skin scaling and thickening due to gene mutations.

Researchers identified specific genes that are important for mouse skin cell development and healing.

The cornified envelope is crucial for skin's barrier function and involves key proteins and genetic factors.

The modified skin board with channels improves skin graft knife performance.

Acne is the most common skin problem in Brazil, with a need for improved dermatological care and health education, especially for the public sector and black-skinned individuals.

Acne was the most common skin problem in kids, with other conditions like warts and eczema also frequent, varying by age and gender.

Using tissue expanders for scalp reconstruction in patients with extensive Aplasia Cutis Congenita is effective and has minimal complications.

The traditional method of estimating skin graft success by looking is generally reliable but less so for inexperienced observers and in certain wound conditions.

Zebrafish are useful for studying and developing treatments for human skin diseases.

A girl with Becker's nevus syndrome showed good improvement in breast development using spironolactone.