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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.

The research suggests that immune cells and a specific type of cell death called ferroptosis are involved in Frontal fibrosis alopecia.

The BUZZ gene is important for root hair growth and overall root structure in the plant Brachypodium distachyon.

Nanomaterials like silver and gold can improve wound healing but need more research for safety.

Cultural awareness in healthcare improves patient care and relationships.

Patients with pernio have lower vitamin B12 and ferritin levels than healthy people.

UV radiation can help sterilize wounds and promote healing but requires careful use to avoid damaging cells.

Forensic DNA Phenotyping can help predict physical traits from crime scene DNA to identify suspects.

The document concludes that systemic autoimmune diseases are complex, incurable, and require ongoing treatment and research.

The document concludes that a new biosensor can efficiently detect prostate cancer cells and that standardized referrals help find significant cancers effectively.

CEC levels may be a useful marker for predicting prostate cancer progression.

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

Methylated gene parts may cause finasteride-resistance in some enlarged prostate patients.

Nellore cattle have genetic variations linked to their adaptation to tropical environments.

Explosions don't stop hair proteins from being used to identify people.

Natural gene therapy shows promise for treating skin disorders like epidermolysis bullosa.

The document concludes that the human keratin gene cluster is complex, with a need for updated naming to reflect over 50 functional genes important for hair and skin biology.

A certain gene variation is linked to a higher risk of polycystic ovarian syndrome in South Indian women.

Scientists turned mouse stem cells into skin cells that can grow into skin layers and structures.

Hair mineral analysis might help diagnose diseases early, but standard methods are needed.

FOXN1 gene variants cause low T cells and immune issues from birth.

Some people experience severe, long-lasting side effects from fluoroquinolone antibiotics, leading to the recommendation of limited use and increased awareness of these risks.

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

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

The conclusion suggests that PCOS may persist due to genetic traits that, while harmful for female fertility, could have provided survival and reproductive benefits to males.

A yeast-based test can detect the steroid methyltestosterone in urine longer than traditional methods.

Low-level laser therapy improves hair growth and dermal papilla cell function.

Progranulin overexpression leads to shorter, thinner hair and increased cell death in mouse hair follicles.

No significant link between CAG repeat numbers and female pattern hair loss in Han Chinese population.

MOF controls key genes for skin development by regulating mitochondrial and ciliary functions.