Search

everythinglearnresearchcommunity

for

Search:↓

Hair loss gene found on chromosome 3q26.

The document concludes that hair transplantation and gene therapy may be important for future hair loss treatment.

Scientists have created a new hair loss treatment using ultrasound to deliver gene-editing particles, which resulted in up to 90% hair regrowth in mice.

Mutations in the WNT10A gene can cause skin, hair, teeth, and other disorders, and may also affect other areas like kidney and cancer, with potential for targeted treatments.

A new gene mutation linked to a skin condition was found in a Spanish family.

Women with lichen planopilaris often have thyroid disease, depression, anxiety, and may respond to treatment with slowed disease progression.

Scalp involvement is common in pemphigus and can lead to hair loss, with the severity of scalp lesions linked to overall disease severity.

Fox Fordyce disease might be more common in prepubertal girls than thought and can be managed with treatment.

Fox Fordyce disease can occur in prepubertal girls and may be underdiagnosed.

Nanotechnology is improving drug delivery and targeting, with promising applications in cancer treatment, gene therapy, and cosmetics, but challenges remain in ensuring precise delivery and safety.

Certain gene variations increase the risk of alopecia areata in Koreans.

Frontal Fibrosing Alopecia might be an autoimmune disease.

Chicken feather gene mutation helps understand human hair disorders.

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

PCOS in lean women is a serious health condition with implications beyond fertility, affecting metabolism and increasing cardiovascular disease risk.

The study found that giant pandas have more melanin in black hair follicles than white, with gene expression differences that could affect hair color and skin health.

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.

The document concludes that understanding hair biology is key to treating hair disorders, with gene therapy showing potential as a future treatment.

A gene network led by RSL4 is crucial for early root hair growth in response to cold in Arabidopsis thaliana.

Hyperandrogenism increases heart disease risk in premenopausal women, but this risk is linked to obesity in postmenopausal women.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

A genetic change in the EDAR gene causes the unique hair traits found in East Asians.

A gene in Arabidopsis thaliana, AtPRPL1, affects root hair length but not cell wall composition.

The document describes a woman with familial Parkinson's disease due to a genetic mutation, showing severe symptoms and poor response to treatment, and suggests finasteride may help reduce symptoms in Tourette syndrome.

Early onset baldness in men may indicate a condition similar to PCOS, linked to heart disease, diabetes, and prostate issues.

Vitamin D and estrogen may help protect heart and kidney health, and maintaining sufficient vitamin D levels could be especially beneficial for African Americans, postmenopausal women, and people with chronic kidney disease.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

Skin doctors should know about skin and kidney disease links to prevent serious kidney problems.

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

Ingenol mebutate gel changes gene expression related to skin development and immune response in actinic keratosis.