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New gene mutations linked to skin conditions were found, bacteria and chemicals may worsen acne, a dog mutation could exist in humans, virus-like elements might be involved in psoriasis, and a vitamin D3 treatment doesn't prevent chemotherapy-related hair loss.

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.

Lactic acid cream can help improve skin bumps known as eruptive vellus hair cysts.

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

Hair, teeth, and mammary glands develop similarly at first but use different genes later.

Permanent hair removal with lasers may cure itchy black hair bristles on the back.

Clouston syndrome is inherited in an autosomal dominant pattern and caused by a specific gene mutation, with no current treatment available.

Human hair keratins K85 and K35 create unique filament patterns important for early hair formation.

Different genes are linked to various types of hair loss.

Monilethrix causes different levels of hair loss in family members.

Early recognition and treatment of VATS in transplant patients improve outcomes.

Ectodysplasin signaling is crucial for skin appendage development, requiring specific doses and durations.

A genetic change in the EDAR gene causes the unique hair traits found in East Asians.

White piedra, a rare fungal infection, was diagnosed in two women in a northern climate.

Cats with abnormal hair had DSG4 gene changes causing hair problems.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

ERG increases SOX9, promoting prostate cancer growth and invasion.

Baricitinib reduces inflammation and improves cell health in premature aging cells.

The symposium highlighted the importance of understanding disease mechanisms for targeted dermatology treatments.

Sox9 is present in most canine skin tumors and may help understand stem cells' role in these cancers.

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

Reflectance confocal microscopy is useful for diagnosing and monitoring skin diseases, but it has limitations and requires expertise for correct use.

Vitamin A helps rabbit skin cells grow and survive heat stress.

Too much β-catenin activity can mess up the development of mammary glands and make them more like hair follicles.

A 2-year-old boy had no hair and unusual organ placement, and it's unclear if it's genetic or coincidental.

MicroRNA-214 is important for skin and hair growth because it affects the Wnt pathway.

The index to ring finger ratio may indicate disease severity in female ankylosing spondylitis patients, but not in males.

Embryonic and adult stem cells are valuable for improving skin grafts and cell therapy.

Noggin overexpression delays eyelid opening by affecting cell death and skin cell development.