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A girl with skin rashes and low zinc levels improved with zinc supplements and had new gene mutations linked to her condition.

MFN2 mutations cause mitochondrial problems, unusual fat distribution, and low leptin despite high body fat.

Gene mutations can cause problems in male genital development.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

A device was made in 2008 to measure hair loss severity. Other findings include: frizzy mutation in mice isn't related to Fgfr2, C/EBPx marks preadipocytes, Cyclosporin A speeds up hair growth in mice, blocking plasmin and metalloproteinases hinders healing, hyperbaric oxygen helps ischemic wound healing, amniotic membranes heal wounds better than polyurethane foam, rhVEGF165 from a fibrin matrix improves tissue flap viability and induces VEGF-R2 expression, and bFGF enhances wound healing and reduces scarring in rabbits.

New genetic locations explain much of hair color variation in Europeans.

The Foxn1 gene mutation causes hairlessness and immune system issues, and understanding it could lead to hair growth disorder treatments.

FGF5 gene mutations cause long hair in domestic cats.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

A mouse gene mutation increases the risk of skin cancer.

Researchers found genes and microRNAs that control curly fleece in Chinese Tan sheep.

The study found key factors in the cause of hidradenitis suppurativa, its link to other diseases, and identified existing drugs that could potentially treat it.

A vitamin D receptor mutation causes rickets and affects immune responses.

Melatonin affects gene expression in goat hair follicles, potentially increasing cashmere production.

Androgen deprivation therapy doesn't lower the risk of death from COVID-19 in prostate cancer patients.

Chicken feather gene mutation helps understand human hair disorders.

Obese mice with a leptin gene mutation have a longer resting phase in their hair cycle, which may help understand certain hair loss conditions.

Cutaneous Lymphadenoma is a unique skin tumor with specific protein markers and common gene mutations that may cause continuous cell growth.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

Scientists found new genetic areas that affect how rice root hairs grow and develop.

The research found key RNA networks that may control hair growth in cashmere goats.

Fasting in hens affects thyroid hormones, which regulate feather and hair growth.

A heterozygous mutation in HTRA1 can cause severe CARASIL symptoms.

Curcumin supplements increase adiponectin and decrease leptin in adults.

The research found a way to grow plant tissue and analyze compounds in Bituminaria bituminosa, which is promising for hair restoration treatments.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

Researchers fixed gene mutations causing a skin disease in stem cells, which then improved skin grafts in mice.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

Melanoma risk tools need improvement, a gene mutation causes a hair disorder that might be treated by managing cell stress, a potential therapy for a skin-ear disorder involves blocking cell channels, skin wrinkling may indicate lung aging regardless of smoking, and oxidative stress might contribute to common baldness.

Melanoma risk tools need improvement, certain gene mutations cause skin diseases and could be treated by targeting those mutations, skin wrinkling may relate to lung aging due to genetic factors, and oxidative stress affects hair loss but can be reduced in low oxygen.