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Adding the topical gel improved hair growth more than using minoxidil or finasteride alone.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

Hair follicle development is controlled by interactions between skin tissues and specific molecular signals.

A20 protein is crucial for normal skin and hair development.

NF-κB is crucial for different stages and types of hair growth in mice.

Keloid skin disorder involves abnormal fibroblast activation and immune response, linked to a group of genes including FGF11.

Nonclassic congenital adrenal hyperplasia is a genetic disorder causing hormone imbalances, affecting fertility and requiring personalized treatment.

Women with nonclassic 21-hydroxylase deficiency can have successful pregnancies through IVF, with certain factors affecting their chances.

Mimicking growth factors in a topical solution can prolong hair growth phase and reduce hair loss without side effects.

Minoxidil helps stabilize hair loss, increase density, and reduce shedding after hair transplant surgery.

New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

The symposium highlighted the importance of understanding disease mechanisms for targeted dermatology treatments.

Doctors should consider Netherton syndrome in patients with chronic skin and hair issues to avoid misdiagnosis.

The 2003 consensus updated PCOS diagnosis criteria and highlighted increased risks of diabetes and heart disease for those affected.

Transplant success has improved with better immunosuppressive drugs and donor matching.

Foxi3 expression in developing teeth and hair is controlled by the ectodysplasin pathway.

Short telomeres contribute to aging and cancer, and while telomerase can delay aging, it may also promote cancer.

A man's rare tumor caused unusual nerve-related symptoms that improved after surgery.

Healthcare providers should start with simple fertility tests and treatments before referring patients to specialists.

Late diagnosis of congenital adrenal hyperplasia can greatly affect physical development, gender identity, and sexual health.

Addressing underrepresentation in Parkinson's research is crucial for better treatments and understanding.

A 23-year-old woman's missed periods were caused by a rare genetic disorder treated with hormone patches.

The 18-year-old girl likely has a condition called müllerian agenesis, which caused her to not have a uterus and experience no menstrual periods.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

Knocking out certain genes in mice helps understand skin and hair growth problems.

TGFα gene mutation in mice causes abnormal skin, wavy hair, curly whiskers, and sometimes eye inflammation.

The JAK/STAT pathway is important in cell processes and disease, and JAK inhibitors are promising for treating related conditions.

Cornification is how skin cells die to form the protective outer layer of skin, hair, and nails.