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

Human hair is unique and important for understanding human evolution and identity.

The conclusion is that grasping how cells determine their roles through evolution is key, with expected progress from new research models and genome editing.

Researchers found two genes that may explain why some Casertana pigs don't have hair.

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.

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.

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

Young women in West Bengal, India, with PCOS often have estrogen resistance, leptin receptor issues, folate deficiency, T2DM, and acanthosis, commonly linked to obesity.

The document concludes that the fast-growing direct-to-consumer genetic testing market lacks sufficient regulation, posing risks to consumers due to questionable test quality and accuracy.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

Keratin-associated proteins have ancient origins and were used for different purposes before being adapted for hair in mammals.

The article concludes that studying how skin forms is key to understanding skin diseases and improving regenerative medicine.

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

A specific protein in chicken embryos links early skin layers to feather development.

Monotreme hair structure and protein distribution are similar to other mammals, but their inner root sheath cornifies differently, suggesting a unique evolution from reptile skin.

New models predict male pattern baldness better than old ones but still need improvement.

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.

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

Hard skin features like scales, feathers, and hair evolved through specific protein changes in different animal groups.

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.

Testosterone is linked to cardiovascular risk factors and stroke, but its exact role is unclear.

Low androgen levels might delay prostate cancer but could lead to more aggressive, therapy-resistant cancers.

More research is needed to understand the genetic causes of Alopecia areata to develop better treatments.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

The research concluded that selection significantly shaped the genetic variation of the X chromosome, with certain regions affected by past selective events.