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Increased HSD11B1 enzyme expression is linked to higher body fat and insulin resistance.

A woman's hair loss and other symptoms were due to a rare hormone deficiency treatable with steroids.

A 36-year-old person with a female appearance but male chromosomes was diagnosed with a rare enzyme deficiency affecting sexual development.

Different Hairless isoforms affect Vitamin D receptor activity in hair regulation, with one repressing and the other stimulating it.

Certain mutations in the hairless protein disrupt its ability to regulate the hair cycle.

Vitamin D receptor and hairless protein are essential for hair growth.

Intense pulsed light with radiofrequency showed mixed results in improving quality of life for hidradenitis suppurativa patients, with no clinical improvements.

Somatic BHD mutations are rare in Japanese renal tumors.

Using electronic health records can help identify drug side effects but has some limitations.

The mutant HR bmh protein affects hair follicle formation by failing to repress vitamin D receptor activity.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

The rs1128977 gene variant may affect cholesterol and body measurements.

The Hr protein binds to DNA, interacts with p53, and affects cell cycle genes.

Hirsute women have lower type 2 17β-HSD enzyme levels, which improve with treatment.

Vitamin D receptor can control the hairless gene linked to hair loss even without vitamin D.

New mutations in the VDR gene cause vitamin D-resistant rickets without hair loss.

SRD5A2 gene variations affect PTSD symptoms differently in males and females.

Manipulating 5α-reductase type 2 can affect liver fat production and glucocorticoid effects.

HPDAlR nanoparticles greatly improve skin wound healing without toxicity.

A rare genetic mutation causes resistance to vitamin D, leading to severe rickets and requiring high doses of calcium and vitamin D for treatment.

Most Hairless gene mutations reduce its ability to work with the Vitamin D Receptor, which might explain a certain type of hair loss.

The hr gene is linked to hair loss in Valle del Belice sheep.

A genetic mutation in the CDH3 gene causes hair loss and vision problems in a young Saudi girl.

"D-CHRAMPS syndrome" is a newly identified condition with multiple severe symptoms.

HS patients rarely see dermatologists, often get opiates, and need better care.

Hydroxypinacolone retinoate is a potent anti-aging ingredient for skin that is more effective and less irritating than other forms of retinoids.

A 72-year-old man was diagnosed with a rare skin form of Rosai-Dorfman disease after years of misdiagnosis.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

Pilonidal sinus disease is linked to more severe hidradenitis suppurativa.

Lack or blocking of SRD5a, a key component in hormone creation, can lead to conditions like pseudohermaphrodism and affect hair growth, bone mass, muscle strength, and reproductive health. More research is needed on its regulation from fertilization to adulthood.