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Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

Faulty LEF1 activation causes faster skin cell differentiation in premature aging syndrome.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

Rogaine can stop hair loss in women, and other treatments like certain pills, light therapy, and special shampoos may also work.

Alopecia areata is an autoimmune disease with genetic links, treatable with certain medications, and can affect mental health.

Over half of young people in Saudi Arabia experience early gray hair, linked to factors like smoking, stress, and family history.

Wearing a toupee makes men seem more attractive and slightly healthier, but doesn't change how confident they appear.

Three specific genetic variants cause severe skin issues in children with EBS, highlighting the need for early genetic screening.

Hair proteins in preschool children and their mothers could indicate developmental changes and health status.

Non-biologic immunosuppressive drugs are crucial for treating autoimmune and chronic inflammatory skin diseases.

Juglone from walnut extracts may help repair damaged hair.

Many pediatric epilepsy patients experience preventable severe adverse drug reactions, especially with certain medications and risk factors.

The document concludes that inflammation markers can be used in diabetes, vitamin D3 affects immune pathways, hyperthyroidism changes hormone levels, androgen levels help diagnose Adrenocortical Carcinoma, erectile dysfunction is linked to diabetes, hypogonadism is common in HIV-infected males, and hormones can be biomarkers for various conditions.

The document concludes that specific methods for making diazine-based drugs can lead to high yields and are important for creating effective treatments for various diseases.

Men with a family history of hair loss on their mother's side are more likely to have female pattern hair loss.

Certain gene variations are linked to the thickness of cashmere goat hair.

An 11-year-old girl with Trichotillomania developed a large hairball in her stomach, treated with medication, therapy, and family education.

An 11-year-old girl with a hair-pulling disorder had a hairball in her stomach and was treated with medication, therapy, and a team of doctors.

Energy healing treatment improved L-cysteine's stability, solubility, bioavailability, and shelf-life.

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

FGF signaling is crucial for starting feather development in chicken embryos.

Barn owls with smaller black spots have higher testosterone levels, which might be due to genetic effects on hormone regulation rather than hormone effects on coloration.

The study found unique microscopic features for hair or feather in five animal ingredients in Shenrongbian pill.

Light tickling can be unpleasant and may feel worse for individuals with autism.

As sheep age, their hair fibers and follicles grow larger and more organized, with no significant differences between males and females.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

Use shallow cuts, small tissue removal, careful suturing, and keep the area moist to reduce scarring in hair transplants.