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The early genes of a specific virus can cause abnormal skin cell growth and hair follicle changes.

Certain gene variations in the Vitamin D Receptor are linked to higher risk of female hair loss.

Skin cells can naturally limit the growth of cancerous changes by balancing cell renewal and differentiation.

HPV 60 may cause cysts and warts on the face, not just hands and feet.

A 17-year-old in Saudi Arabia was diagnosed with a rare skin condition causing red-brown facial patches.

Some women with PCOS have CYP21 mutations and IRS1 variants, but these genetic factors are not major contributors to PCOS.

The gene NM_026333 slows down aging by affecting the NCX1 pathway and could be targeted for anti-aging treatments.

Hereditary hyperplastic gingivitis in silver foxes may be linked to errors in the MAPK signaling pathway, influenced by androgens.

A KRT32 gene variant causes loose anagen hair syndrome.

MCHR2 gene duplications may be linked to alopecia areata.

MEK and BRAF inhibitors increase sebum production and accumulation, which could cause acne-like side effects.

Genetic testing for cancer risk can lead to early and life-saving treatments in people without symptoms.

Graying hair is caused by changes in gene expression affecting cell functions.

Overexpression of E2F1 can lead to skin tumors and disrupt hair growth.

Mutant keratins cause inflammation in Epidermolysis Bullosa Simplex, suggesting targeting them could help treat the disorder.

A new type of pachyonychia congenita may exist, caused by a different keratin mutation.

The condition might be caused by genetic changes after birth.

A specific genetic marker is linked to male pattern baldness in Han Chinese men.

Frontal fibrosing alopecia has occurred in two related male families.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

Axitinib treatment turned a man's grey hair back to black.

Different hair fiber development might explain why hair loss severity varies in patients with a specific genetic mutation, and treatments that thicken hair could help.

A new goat gene affects cashmere fiber thickness; certain variations can make the fibers coarser.

BKN-1 antibody targets specific keratin in basal cell epithelioma and normal skin basal cells.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

A new change in the WNT10A gene caused a condition leading to short hair growth in a Chinese family.

Lipid-antigen stimulation may play a role in folliculotropic mycosis fungoides.