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The study aims to understand the skin and hair characteristics of mothers and their babies, and how these may affect newborns' skin health and mothers' postpartum hair loss.

Mutations in the vitamin D receptor cause hereditary vitamin D-resistant rickets, leading to poor bone health and requiring high calcium doses for treatment.

Damaging mutations in NFKB2 cause a severe and distinct form of primary immunodeficiency with early-onset and often ACTH-deficiency.

Heavily hunted wolves have higher stress and reproductive hormone levels.

The review suggests that other immune cells besides CD8+ T cells may contribute to alopecia areata and that targeting regulatory cell defects could improve treatment.

Teriflunomide effectively reduces relapse rates and disease progression in multiple sclerosis but is not safe for use during pregnancy.

BMP signaling is essential for the development of touch domes.

Thallium, mercury, selenium, and colchicine strongly cause hair loss.

Zebrafish need MYC and FGF to regenerate inner ear hair cells.

Isotretinoin can cause serious birth defects and needs careful use, especially in pregnant women.

Many women with hair loss also have thyroid issues, high blood pressure, and low Vitamin D.

Child abuse is linked to higher BMI, but not because of hair cortisol or cortisone levels.

Mouse tail skin has different keratinization near hair follicles and scales.

Adding a second method to PROTACs could improve cancer treatment.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

Skin cells show flexibility in healing wounds and forming tumors, with potential for treating hair disorders and chronic ulcers.

Inherited color dilution in rabbits is linked to DNA methylation changes.

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

Organic and biogenic nanocarriers can improve drug delivery but face challenges like consistency and safety.

Androgenetic alopecia in teens is linked to obesity and other metabolic risks, needing early diagnosis and management.

Girls had higher stress hormone levels during school due to social and emotional issues, while boys had higher overall hormone levels with slight changes when school started.

An 11-year-old boy in Saudi Arabia has a rare case of hypoparathyroidism with severe brain calcifications but normal development and no known cause.

Bioinspired polymers are promising for advanced medical treatments and tissue repair.

Some hair protein genes evolved early and were adapted for use in hair follicles.

Some women with PCOS have rare genetic variants linked to the condition.

Early recognition and treatment of tinea capitis are crucial to prevent severe scalp issues and prolonged therapy.

Scabies is the most common skin condition among children in Pakistan, with poor hygiene and contact with animals being major risk factors.

A heterozygous mutation in HTRA1 can cause severe CARASIL symptoms.

A new goat gene affects cashmere fiber thickness; certain variations can make the fibers coarser.

Certain immune-related proteins are higher in people with alopecia and their healthy relatives, hinting at a genetic link.