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Researchers found a way to grow cashmere goat hair cells in a lab and discovered that certain conditions improve these cells' growth and characteristics.

Mutations in the RBPJ gene cause Adams-Oliver Syndrome.

KAP genes show significant genetic variability, but its impact on hair traits is unclear.

The genes KRT25 and SP6 affect curly hair in horses, with KRT25 also causing hair loss. If both genes are mutated, the horse gets curly hair and hair loss. KRT25 can hide the effect of SP6.

CRABP2 helps increase the growth of cells important for hair growth by activating a specific growth pathway.

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

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.

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

Four patients with a type of rickets and hair loss had different mutations in their vitamin D receptor gene, causing it to not work properly.

PAD3 plays a key role in hair and skin protein structure and may be linked to skin diseases.

Researchers identified genes linked to coat color, body size, cashmere production, and high altitude adaptation in goats.

The study found that immune responses disrupt hair growth cycles, causing hair loss in alopecia areata.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

Hair problems can be caused by genetics or the environment, and treatment should focus on the cause and reducing hair damage.

An 11-year-old Greek girl was diagnosed with a rare genetic disorder, highlighting the importance of genetic testing and family history.

The LRRK2-G2019S mutation in Parkinson's disease has a lifetime penetrance of 25-35%, and finasteride may help reduce symptoms in adult male Tourette syndrome patients.

Finasteride reduces Tourette syndrome symptoms, but results may be limited due to potential biases.

Finasteride may help reduce symptoms in male Tourette syndrome patients.

The document describes a woman with familial Parkinson's disease due to a genetic mutation, showing severe symptoms and poor response to treatment, and suggests finasteride may help reduce symptoms in Tourette syndrome.

Finasteride significantly reduced tics and obsessive-compulsive symptoms in patients with Tourette syndrome.

Different combinations of human hair keratins affect how hair fibers form.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

Finasteride negatively affects fish reproduction and gonadal development.

Finasteride significantly reduced tics and obsessive-compulsive symptoms in Tourette syndrome patients.

Finasteride may help reduce tic severity in male Tourette syndrome patients.

A woman's unique dementia was misdiagnosed, a genetic mutation increases Parkinson's risk with age, and finasteride may help with Tourette syndrome.

TRPV3 could be a target for treating pain, skin disorders, and hair problems, but more research is needed to create effective drugs.

Human hair loss may have evolved to help increase brain size.

Self-assembling RADA16-I hydrogels with bioactive peptides significantly improve wound healing.

Some hair protein genes evolved early and were adapted for use in hair follicles.