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Androgen-deprivation therapies increase the risk of certain heart conditions, but testosterone treatment may help.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

PCR genotyping in cre-loxP mice can be inaccurate due to unintended gene deletions in non-target tissues.

Genetic variation in the KRTAP15-1 gene affects wool yield in sheep.

TNFα, IFNγ, and Substance P significantly affect prolactin levels in human skin, suggesting new treatments for skin and hair conditions.

PMC shows promise as a treatment for hair loss.

A specific gene variation is linked to a higher risk of polycystic ovary syndrome in Caucasian women.

Certain gene combinations may affect prostate cancer risk, and GSTP1 methylation is linked to tumor aggressiveness.

Liver transplantation is a viable option for children with propionic acidemia, improving quality of life and diet, but does not remove all risks and long-term brain outcomes are uncertain.

Two new gene mutations cause a rare hair disorder.

Women with PCOS have higher levels of certain blood clotting factors, suggesting a greater risk of cardiovascular issues.

A new method allows for controlled, long-lasting delivery of retinoic acid through the skin with fewer side effects.

CT60 polymorphism might increase the risk of Alopecia Areata.

Budesonide and N-acetylcysteine reduced tumors and alopecia in mice, regardless of FHIT gene status.

People from iodine-deficient areas are more likely to develop hypothyroidism when treated for multi-drug resistant tuberculosis.

High TNF-α levels may increase hair loss risk after PRP therapy.

CTA is often mistaken for AA but doesn't respond to steroids and may require hair transplantation.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

STK11 gene polymorphism does not predict metformin response in PCOS.

A boy with Pachyonychia congenita has a confirmed gene mutation, highlighting the need for a local genetic database in India.

Truncated LTBP-1 disrupts TGF-beta signaling, affecting hair growth.

The new platinum complexes effectively increased survival in rats with tumors, despite some reversible side effects.

Retinoids or their analogs could treat skin pigmentation disorders like melasma and vitiligo.

Longer TA repeats in the SRD5A2 gene may increase acne risk in Chinese people.

A mutation in the MAP2 gene causes reduced hair follicle density, leading to hairlessness.

The patient's hair improved after treatment, but the genetic link is unclear.

Certain genes in Iranian sheep are linked to wool production and heat adaptation.

No link found between specific genes and female pattern hair loss.

Topical immunotherapy with DPCP is most effective for certain alopecia areata types, with success linked to age and disease duration, and influenced by a gene polymorphism.