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A hair-growth formula with cystine and thiamin helps protect skin cells against UV damage and improves their growth.

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

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

ZDHHC13 is important for normal liver function and metabolism, affecting mitochondrial activity.

CCC1 is essential for ion balance and proper plant cell function.

A specific gene mutation causes sparse, brittle hair in a family.

Mettl3 is essential for normal tissue development and self-renewal by regulating gene expression.

A specific gene mutation causes a severe skin disorder in a family.

The study found no common cause for a girl's crystalline cataract and uncombable hair, suggesting their co-occurrence might be coincidental.

CNGA3, GLUD1, and SIRT1 are promising targets for treating aging and glioblastoma.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

ATR12-351 ointment safely delivers LEKTI protein to the skin, reducing enzyme activity in Netherton syndrome.

CD98hc's role in skin health decreases with age.

ABCD1 gene mutations cause adrenomyeloneuropathy, leading to symptoms like limb weakness and spasticity, with management focusing on rehabilitation and spasticity treatment.

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

Lymphoid-specific helicase (Lsh) is crucial for skin growth, change, and healing after injury.

PAD3 plays a key role in hair and skin protein structure and may be linked to skin diseases.

Lysosomal proteases and cytoplasmic enzymes help hair follicle cells develop and differentiate.

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

Perming and bleaching damage hair differently, with bleached hair having more cysteic acid in the cuticle.

MG53 helps reduce skin damage caused by nitrogen mustard.

L-Cystine and L-Cystine with Kera-Diet® safely improved hair and nail quality in healthy women.

PROTACs offer a new, precise way to treat cancer by breaking down harmful proteins.

A bull with a gene mutation was asymptomatic, synthetic retinoids cause hair loss, and new therapeutic targets were identified for skin diseases.

Slug is crucial for skin health, hair growth, and healing.

Changes in genes FGA, VWF, and ACTG1 may contribute to pemphigus vulgaris.

CTHRC1 is essential for healing and preventing heart rupture after a heart attack.

A boy's growth and immune problems were caused by a new mutation in the STAT5B gene.

Genetic testing is crucial for diagnosing and managing non-Herlitz junctional epidermolysis bullosa.

The new method is 1000 times more sensitive for measuring hair growth.