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Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

The ethanol patch test reliably identifies ALDH phenotype.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

Certain HSD3B1 gene types are linked to worse prostate cancer outcomes and affect treatment response and other health conditions.

A man with X-ALD improved after treatment, highlighting the need to consider X-ALD in similar patients and test their relatives.

A49T gene variant linked to higher prostate cancer risk, lower hormone levels, and slightly reduced balding risk.

The enzyme Dgat1 is essential for healthy hair and skin by controlling retinoid levels.

The Rotterdam Study found risk factors for elderly diseases, links between lifestyle and genetics with health conditions, and aimed to explore new areas like DNA methylation and sensory input effects on brain function.

The research identified various cell types in mouse and human teeth, which could help in developing dental regenerative treatments.

Birds can lose neck feathers due to a genetic change that increases a gene's activity, helping them adapt to heat.

Maintaining the right amount of retinoic acid is crucial for healthy hair and skin.

Noncoding dsRNA boosts hair growth by activating TLR3 and increasing retinoic acid.

Blocking TGFβ-RI signaling enhances surface ectoderm differentiation from human stem cells.

Arctiin helps protect hair cells from damage and death caused by oxidative stress.

Eating vitamin A affects hair growth and health by changing cell signals in mice.

Troxerutin helps protect skin cells from oxidative stress and may be good for treating hair loss.

Key genes can rewire networks, changing skin appendage types.

Transplanting growing hair follicles into scars can help regenerate and improve scar tissue.

Activating TLR3 may help produce retinoic acid, important for tissue regeneration.

All-trans retinoic acid at high doses harms goat hair growth cells and could be bad for hair growth.

Genetic variations affect dutasteride treatment response for male pattern hair loss.

A short male anogenital distance may indicate incomplete masculinization due to disrupted androgen action.

The April 2014 issue of "Fertility and Sterility" discussed various reproductive health topics, including hormone therapy benefits, sperm and genetic factors in male infertility, and the link between PCOS and diabetes.

New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.

A genetic mutation in a specific gene causes a salt-wasting condition in a Pakistani girl and her family.

Certain genetic variants impair enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

Researchers found a new mutation causing total hair loss from birth.

ACOD1 deficiency worsens hair loss by causing cell aging and mitochondrial problems, but 4-OI may help.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

CLEC4D gene variants may increase the risk of alopecia areata in Jordanians.