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The research found specific genes and proteins that affect how fast chickens' feathers grow, which is not solely determined by traditional inheritance patterns.

Certain gene variations are linked to a higher risk of severe acne, suggesting a genetic influence on the condition.

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

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

Blond hair in Solomon Islanders is due to a unique genetic variant, not European ancestry.

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

The article concludes that the wool follicle is a valuable model for studying tissue interactions and has potential for genetic improvements in wool production.

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

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

FFA's causes may include environmental triggers and genetic factors.

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

Some hair loss disorders are caused by genetic mutations affecting hair growth.

Genetic variations greatly affect individual metabolism and can impact health and disease risk.

Acne is significantly influenced by genetics, and understanding its genetic basis could lead to better, targeted treatments.

Genetic marker rs12558842 strongly linked to male hair loss.

Genetic variants linked to ten skin diseases were found, showing both immune and non-immune factors play a role.

Genetic research has advanced our understanding of skin diseases, but complex conditions require an integrative approach for deeper insight.

Genetic discoveries are leading to new treatments for alopecia areata.

Genetic discoveries are key for understanding, diagnosing, and treating inherited hair and nail disorders.

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

A rare genetic mutation found in an Indian family can be detected through prenatal screening.

A certain genetic variation in the IL1A gene may lower the risk of a hair loss condition in Chinese people.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

Two siblings with a genetic mutation had a form of rickets that doesn't respond to vitamin D.

A 12-year-old boy with a rare genetic condition has progressive hair loss with no effective treatment.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

Certain genes are linked to the quality of cashmere in goats.

FGF10 and non-coding RNAs are important for cashmere goat hair follicle development.

Certain miRNAs are linked to chicken feather development.