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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.

Patients with Systemic Sclerosis have much higher levels of GDF-15, which could help predict organ involvement and guide treatment.

The CORT, FGF5, and CD36 genes are crucial for the cold weather adaptation of Yanbian cattle.

Researchers found two new genetic variants linked to Alzheimer's disease.

JAGGED1 could help regenerate tissues for bone loss and heart damage if delivered correctly.

ZDHHC13 is important for normal liver function and metabolism, affecting mitochondrial activity.

Blocking the androgen receptor in skin cells reduces their growth response to male hormones, suggesting a possible treatment for skin conditions linked to androgens.

Immune cells affect hair growth and could lead to new hair loss treatments.

Injecting CHIR-99021 into goose embryos improves feather growth by changing gene activity and energy processes.

Hairless mammals have genetic changes in both their protein-coding and regulatory sequences related to hair.

FLCN helps control iron levels in cells.

A specific genetic deletion in goats affects cashmere yield and thickness.

Testosterone and dihydrotestosterone treatments can help with penile growth in males with 5α-reductase type 2 deficiency, with dihydrotestosterone being more effective in infancy.

A boy and his father with hereditary hypotrichosis simplex were treated for hair loss, but the treatment result is unknown.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

HNG may help prevent the negative effects of chemotherapy on sperm production and white blood cell counts.

The document suggests a bacteria plays a significant role in acne rosacea and that white hair can regain color after transplant, meriting more research on reversing grey hair.

Lower adrenal hormone levels may cause hair loss in postmenopausal women, certain patterns help diagnose nail cancer, and a gene variant linked to higher skin cancer risk in kidney transplant patients suggests monitoring folate levels.

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

Cells lacking the Bax protein can outcompete others, leading to better tissue repair and hair growth.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

Certain skin proteins can form anchoring structures without the protein AMACO.

The TRPV3 gene variant may cause the long-haired suri alpaca coat.

Hair color is determined by melanin produced and transferred in hair follicles.

Low selenium levels can extend lifespan but worsen health issues.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

The UD-PrOZA program successfully diagnosed 18% of adult patients with rare diseases, often using genetic testing.

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

Different genes are active in dogs' hair growth and skin, similar to humans, which helps understand dog skin and hair diseases and can relate to human conditions.

Foxn1 gene regulation is crucial for thymus development but not for hair growth.