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Physiology education needs to include more diversity and different perspectives to better represent all populations.

The convention discussed various skin conditions, treatments, and the importance of continuous learning in dermatology nursing.

Polycystic Ovary Syndrome (PCOS) affects 6%-15% of women of reproductive age, causing symptoms like acne and hair loss, and increasing the risk of type 2 diabetes and heart disease; it's managed through diet, exercise, and medications like Metformin and hormonal contraceptives.

Environmental factors like diet and vitamin levels, especially Vitamin D, can affect autoimmune diseases differently, with lifestyle changes potentially improving outcomes.

The research found that genetic factors for male pattern baldness in African men differ significantly from those in Europeans.

Certain genetic variations are linked to hair loss in Mexican men.

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

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

A genetic marker linked to a type of hair loss was found in most patients studied.

Crossbreeding improves goat fiber quality, and specific genes affect hair traits and color.

Researchers found a genetic region that influences the number of coat layers in dogs.

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

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

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.

Estrogen and androgenic hair increase melanoma risk, especially in European-ancestry individuals.

Certain genetic variants linked to immune response increase the risk of alopecia areata in Taiwanese people.

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

Wild African goats have genetic adaptations for surviving harsh desert conditions.

Non-classic congenital adrenal hyperplasia (NCCAH) can mimic PCOS and requires genetic testing for proper diagnosis and treatment.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

Fish teeth and taste bud densities are linked and can change between types due to shared genetic and molecular factors.

Future research on ectodysplasin should explore its role in diseases, stem cells, and evolution, and continue developing treatments for genetic disorders like hypohidrotic ectodermal dysplasia.

Genes related to pigmentation, body rhythms, and behavior change during hares' seasonal coat color transition, with a common genetic mechanism in two hare species.

Early diagnosis and individualized treatment improve outcomes for Congenital Adrenal Hyperplasia.

Keratins are important for skin cell health and their problems can cause diseases.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

Hairlessness in mammals is due to complex genetic changes in both genes and regulatory regions.

Modern lifestyles, including poor diet, stress, and long-term use of certain medications, hinder the body's ability to heal from inflammation, leading to chronic diseases.

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.