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A new accurate and reliable method was developed to measure Spironolactone and Hydrochlorothiazide together in medicines.

Retinoic acid affects skin and hair health by working with specific receptors, and its absence can lead to hair loss and skin changes.

The trichohyalin gene is located at chromosomal region 1q21 with other skin-related protein genes.

SP1 promotes and KROX20 inhibits hair cell growth by affecting the CUX1 gene.

Mutations in the LIPH gene cause woolly hair in a child.

Eclipta alba IIHR Sel EA 43 is best for large-scale cultivation due to high growth, yield, and wedelolactone content.

The 308-nm excimer laser is a promising treatment for vitiligo with varying success and mild side effects.

Topical IKKα inhibitors may help prevent CCS tumours.

EDA2R is a key gene linked to ageing and diseases, and targeting it may help treat conditions like hair loss and chronic diseases.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

ROXY proteins help plants respond to nitrate shortage by affecting nutrient sensing and growth.

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The vitamin D receptor has many roles in the body beyond managing calcium, affecting the immune system, hair growth, muscles, fat, bone marrow, and cancer cells.

Two patients with Cronkhite-Canada syndrome achieved remission after treatment.

The mutant HR bmh protein mis-localizes in cells, affecting skin and hair development.

PRC1 is essential for proper skin development and stem cell formation by controlling gene activity.

Wrinkled skin in Xiang pigs is linked to gene changes related to oxidative stress and the extracellular matrix.

A common mutation in the hHb6 gene is linked to monilethrix, but other factors may also play a role.

A new protein, mK6irs, is found in specific hair layers and may help understand hair growth and diseases.

The mutated hairless gene causes hair loss by acting as a new type of corepressor affecting thyroid hormone receptors.

RNase L hinders hair follicle regeneration by altering immune signals.

Hoxc13 gene is essential for hair, nail, and papilla development.

The RORα gene is active in different parts of cashmere goat hair follicles and may be influenced by melatonin, especially in December when hair growth changes.

Lhx2 is essential for effective Sonic Hedgehog signaling in early retinal development.

Rothmund-Thomson syndrome type 2 can cause chronic, poorly healing wounds.

Targeting regulatory T cells may help treat age-related diseases.

A specific gene variation increases the risk of high uric acid and cholesterol in young Mexican males.

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