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Six new risk spots for early hair loss were found, which also link to Parkinson's disease and lower fertility. Two genes, FOXA2 and HDAC4, could be new treatment targets. Hair loss might also be connected to heart disease, metabolic syndrome, and prostate cancer.

Mice without the p21 gene can fully regenerate injured ears due to reduced Sdf1 increase and leukocyte recruitment, suggesting new ways to induce tissue regeneration in mammals.

Male pattern baldness involves hormones and cell signals affecting hair growth.

The document concludes that there are no effective clinical treatments for hearing loss due to hair cell damage, but research is ongoing.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

Humans lost body hair relatively recently in evolution.

Genetics play a role in acne, but how exactly they contribute is not fully understood.

Genetic defects and UV radiation cause skin damage and aging.

Hormones and their receptors, especially androgens, play a key role in hair growth and disorders like baldness.

Mutations in the androgen receptor gene cause Androgen Insensitivity Syndrome, affecting sexual development.

Hair loss patterns differ between males and females due to 5 master regulators and JAK-STAT signaling affects hair growth.

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

Some domesticated animals have the same genetic skin diseases as humans, which can help doctors understand human genetic mutations.

Newborn screening and gene therapy are expected to improve outcomes for Omenn syndrome patients.

Low-coverage sequencing is a cost-effective way to identify genes related to wool traits in rabbits.

Finasteride blocks progesterone's effect on absence seizures in rats.

Melatonin improved mental health and metabolism in women with PCOS.

The study found that diseases can be grouped by symptoms and that the accuracy of predicting disease-related genes varies with the data source.

Progesterone and related compounds may help control seizures linked to the menstrual cycle but have limitations that need addressing.

Two rare genetic diseases cause severe rickets in children due to defects in vitamin D metabolism.

The study concluded that testing hormone levels after stimulation is not reliable for identifying carriers of 21-hydroxylase deficiency; genetic testing is necessary.

The baby’s hair loss was due to a rare genetic condition, not treatable by usual methods.

Genetic testing is crucial for diagnosing congenital atrichia, a rare condition causing irreversible hair loss.

The meeting highlighted the importance of genetic testing and multidisciplinary approaches in pediatric dermatology.

Men with genetic hair loss are more likely to have abnormal blood lipid levels, especially if the hair loss is severe.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

Feather patterns form through genetic and epigenetic controls, with cells self-organizing into periodic patterns.

Mutant mice help researchers understand hair growth and related genetic factors.

Hidradenitis suppurativa is caused by genetic factors, inflammation, bacteria, hormones, and lifestyle factors like obesity and smoking.