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Some hair proteins are specific to hair, while others are also found in skin cells.

A new method allows for controlled, long-lasting delivery of retinoic acid through the skin with fewer side effects.

A patient's grey hair regained color during treatment with adalimumab.

The issue covers reproductive health topics like cancer markers, incontinence treatments, and the impact of pre-term birth.

PRP may improve fertility treatment success but needs more research for safe use.

CD4 T cells need IFN-γ to cause hair loss in alopecia areata.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Certain gene variations are linked to higher male hormone levels in Chinese women with PCOS and insulin resistance.

A new EDA gene variant causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family.

The enzyme 5α-reductase is important for proper blood vessel development during the fertility-related transformation of the uterus lining.

An 87-year-old woman was diagnosed with type 3 autoimmune polyendocrine syndrome and had multiple autoimmune issues.

Bacteroides fragilis and Microbacterium sp. T32 may be linked to autoimmune activity in Hashimoto's thyroiditis and alopecia areata.

Topical corticosteroids are the best initial treatment for children with Alopecia Areata.

Mouse hair follicle stem cells can help prevent Type 1 Diabetes.

Allopregnanolone increases KCC2 expression in baby male rats' brains, while finasteride doesn't affect it.

Lower adiponectin levels are linked to higher insulin resistance in women with PCOS.

Changes in genes FGA, VWF, and ACTG1 may contribute to pemphigus vulgaris.

Pemphigus vulgaris involves specific immune cells and B cells that produce antibodies causing skin blisters.

The new antibody, TYHF-1, specifically targets certain hair-related structures.

TCF7L2 gene polymorphism is linked to alopecia areata, but it doesn't affect the success of PRP or conventional treatments.

Androgens may influence T cells, contributing to higher autoimmune liver disease risk in women.

A woman developed vitiligo from repeated eyebrow microblading.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

Mutations in mitochondrial DNA might significantly contribute to the development of Polycystic Ovarian Syndrome.

The enzyme 5α-reductase type 1 is important for blood vessel development and fertility in the uterus.

Shock can be an early sign of Autoimmune Polyendocrine Syndrome Type II.

Normal-range ALT levels can indicate metabolic and hormonal imbalances in young women.

The mTurq2-Col4a1 mouse model shows how the basement membrane develops in live mammals.

People with polycystic ovary syndrome have a higher chance of having chronic thyroiditis.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.