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A Korean boy's skin and digestive symptoms were caused by a rare genetic disorder that affects zinc absorption, and he got better with zinc supplements.

CD3+ T-cell presence is a reliable marker to tell apart alopecia areata from pattern hair loss.

Diphencyprone helped most patients with alopecia areata regrow some hair.

Oral contraceptive use may increase the risk of frontal fibrosing alopecia in women with a specific CYP1B1 gene variant.

Two patients with stubborn hair loss grew hair after PDRN injections.

Zinc supplements improved the girl's skin and hair condition.

The document confirms the structures of major metabolites of the CRTh2 antagonist Setipiprant and identifies minor metabolites.

Platycladus Orientalis leaf vesicles may help treat anxiety, depression, and insomnia.

A woman's rare scalp condition worsened after using a specific arthritis medication, suggesting such medications can sometimes trigger or aggravate psoriasis.

A 12-year-old girl's hair loss was linked to a rare genetic condition called ALX4-related frontonasal dysplasia.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

Trichohyalin is modified by enzymes to form strong structures in hair cells.

Cepharanthine effectively reduces Herpes Simplex Virus Type 1 by blocking certain cell pathways and promoting cell death.

HPE may help treat osteoarthritis by promoting cartilage regeneration.

Periplaneta americana extract helps hair regrowth in alopecia areata by reducing inflammation and balancing skin bacteria.

Certain genetic variants in keratins increase the risk of tooth decay.

A girl with Pitt-Hopkins syndrome developed curly hair as a rare side effect from the epilepsy drug perampanel.

Human and horse hair have similar end groups to wool and feathers.

Krt16-deficient mice help understand skin disorders like PC and FNEPPK.

Epiprofin suppresses parathyroid hormone gene activity, helping regulate calcium levels and could be a treatment target for hyperparathyroidism.

The 595-nm pulsed dye laser effectively reduces symptoms of EFFC with minimal side effects.

A mutation in the HOXC13 gene causes hair and nail problems in a Syrian family.

Untreated Congenital Adrenal Hyperplasia can cause severe hair loss due to high androgen levels.

Too much parathyroid hormone-related protein in skin disrupts hair growth in mice.

sPLA2-X is crucial for normal hair growth and follicle health.

DCPA is a chronic skin condition affecting the lower limbs, mainly in men, with unclear causes and treatments that often don't work well.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

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

TCDD speeds up skin barrier formation by increasing certain gene expressions.

Unified regulations and ethical guidelines are needed for fair use of forensic DNA phenotyping.