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The gene LRRC15 is more active in balding areas of the scalp compared to non-balding areas.

Lysine carboxymethyl cysteinate (LCC) protects skin from UVB damage by activating autophagy.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

A genetic mutation in the hHa1 gene creates a smaller, but still functional, hair protein without causing hair problems.

Hairless protein reduces Msx2 gene activity, affecting hair follicle development.

A child has a rare hair and skin disorder due to specific gene variants, suggesting broader genetic testing is needed.

The research found that a specific gene mutation causes fewer hair follicles and disrupted hair growth cycles, leading to thin and short hair in people with Hypotrichosis with Juvenile Macular Dystrophy.

Two patients with the same genetic mutation had both blistering skin and easily pulled out hair.

A boy with long QT syndrome was treated successfully, highlighting the need for careful evaluation of chest pain in children for heart conditions like LQTS.

Lichen planus pigmentosus mainly affects middle-aged women with darker skin, is underreported, and is hard to treat.

A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.

Lactobacillus acidophilus substances can kill and stop the spread of cervical cancer cells.

Most low-level light therapy studies did not accurately report how light was measured, affecting treatment reliability.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

Hair differentiation starts earlier than thought, involving multiple type-II keratins.

Lymphatic vessels and hair follicles interact and may influence hair growth.

A mutation in the iRhom2 gene causes hairless mice due to abnormal hair follicle development.

New mutations in the VDR gene cause vitamin D-resistant rickets without hair loss.

Genetic testing confirmed a rare disorder causing hair loss and vision problems in a Saudi family, stressing its importance for diagnosis and counseling.

Low-dose oral minoxidil increases hair thickness and length in children with a hair disorder called Loose Anagen Hair Syndrome.

Surgery removed an ovarian tumor, improving her symptoms and normalizing testosterone levels.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

Taking riboflavin and eating less lysine can help some people with a specific genetic disorder avoid brain damage.

The study developed a reliable method to measure active ingredients in hair nourisher products using HPLC.

Combining low-level laser therapy and exosome therapy promotes hair growth.

Hairless protein helps control hair growth by regulating vitamin D receptor activity.

The new anti-aging ingredient improves skin hydration, elasticity, and reduces wrinkles.

Type I and Type II keratin chains can form heterodimers despite sequence differences.

The May issue discussed publishing agreements and four studies on cholesterol in hair, cancer cell changes, hormones in the uterus, and skin protein effects.