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Skin cells from people with Epidermolysis Bullosa Simplex have abnormally placed and less active mitochondria.

Research on Hutchinson-Gilford progeria syndrome could help understand normal aging and heart disease.

Side effects of drugs can lead to the discovery of new treatments.

Dihydrotestosterone has a reduced effect on muscle-building in people with testicular feminization syndrome, especially after their gonads are removed.

Monilethrix is a genetic disorder causing brittle hair, diagnosed using tricoscopy.

Histone demethylases play a key role in the development of many diseases and may be targets for treatment.

Twist2 is essential for scarless skin healing and hair growth in mouse fetuses.

Twist2 is essential for proper skin healing and hair growth in developing mice.

Early diagnosis of GLPLS is crucial to prevent complications, but scarring alopecia is irreversible.

A protein called GIS3 is important for the growth of root hairs in Arabidopsis by controlling two genes with the help of certain growth signals.

Low-intensity ultrasound may protect hair follicles from damage caused by a common chemotherapy drug.

An infant with complete hair loss was diagnosed with a genetic disorder affecting hair growth.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

Two siblings with a rare type of rickets and hair loss had low vitamin D levels, which is not typical for their condition.

A 23-year-old woman's missed periods were caused by a rare genetic disorder treated with hormone patches.

Neutrophil extracellular traps slow down hair follicle healing after injury.

Loose anagen syndrome causes easy hair shedding in children, often resolving on its own.

Androgens increase norepinephrine release, promoting smooth muscle growth in male sex organs, which may contribute to benign prostatic hypertrophy.

The study found that tight junctions reach the top layer of the skin's stratum granulosum, not just the second top layer as previously thought.

Ovol2 is important for proper skin healing and hair growth.

Bovines can have rare inherited skin diseases with specific symptoms like hair loss, fragile skin, and abnormal porphyrin buildup.

Classifying alopecia helps diagnose and treat different types of hair loss accurately.

Certain gene mutations can weaken the skin barrier and, when combined with environmental factors, lead to eczema and severe itching.

Vitamin D3 and its receptor are important for hair growth, and understanding receptors could help treat hair graying and skin cancer.

The UK Intellectual Property Office allows granting of supplementary protection certificates with negative terms.

Mutations in the glucocorticoid receptor gene cause reduced sensitivity to glucocorticoids and may lead to poor response to treatment.

Hair graying is caused by the loss of pigment cells due to poor maintenance of stem cells in the hair follicle.

Copper treatments increase copper in all tissues, but brindled female mice accumulate much more copper in their kidneys without clinical effects, unlike brindled male mice where brain copper deficiency is clinically significant.

Artemis dysfunction might cause hair loss through telomere shortening.

Cepharanthine, a Japanese hair loss drug, shows promise as a COVID-19 treatment but needs more testing.