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Electron Beam Tomography (EBT) is a useful additional test to stress testing for detecting heart disease.

Increased TEMRA cells can predict treatment outcomes in rapidly progressive alopecia areata.

Some types of hair loss can continue for a long time after recovering from a severe drug reaction known as DRESS.

A new treatment using AGED to modulate PPAR-γ shows promise for treating scarring hair loss by protecting and repairing hair follicle cells.

EPDS and MS might share an immune-related cause.

Dkk4 protein helps control how hair grows and its arrangement.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

The study found that combining different databases gives a better estimate of drug side effects in hospitals.

Chromosomal microarray analysis is important for diagnosing rare genetic variations and guiding treatment.

Vitamin D receptor binds similarly to natural and synthetic ligands, affecting gene regulation.

TGF-β2 plays a key role in human hair growth and development.

Lack of Vitamin D receptor changes skin structure and increases certain immune cells in the skin.

Dutasteride helps reduce heavy drinking, especially for those who drink to cope.

Early diagnosis and genetic counseling are crucial for managing adrenoleukodystrophy.

The document sets criteria for diagnosing long-term sexual dysfunctions caused by certain medications.

rPanglaoDB helps study rare cell types by merging RNA data, showing fibrocytes aid in healing.

The research found specific genes that are more active in balding cells, which could be causing hair loss.

Platelet-rich plasma helps heal second-degree burns and reduces scarring.

Scientists identified a group of human skin cells with high growth and regeneration potential.

Pregnancies in a woman with the Donohue mutation were managed with genetic testing, resulting in three healthy infants.

Finasteride and dutasteride's effects are mainly due to target binding saturation and slow enzyme turnover.

A new genetic mutation was found causing hair and eye issues in a boy.

Low-dose dutasteride effectively and safely promotes hair growth in men.

PDCD4 is important for controlling skin cell growth and healing.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

A 2-year-old boy was diagnosed with a rare genetic condition causing fragile hair, intellectual issues, and short stature.

Two new gene mutations cause a rare hair disorder.

Many people had severe allergic reactions to a common hair dye ingredient, causing them to seek medical care and miss work.