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

SRD5A2 gene variations affect PTSD symptoms differently in males and females.

Low-dose glucocorticoid treatment improves pregnancy and birth rates in women with nonclassical 21-hydroxylase deficiency.

New mutations in the EBP gene cause CDPX2, affecting bones, skin, eyes, and hair, with females generally less affected than males.

Mutations in the KRT85 gene cause hair and nail problems.

Gene variations may increase oxidative stress in male pattern baldness.

A new gene, JMJD1C, may affect testosterone levels in men.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

A new goat gene affects cashmere fiber thickness; certain variations can make the fibers coarser.

GABRA2 gene variations impact alcohol response, and hair loss medication finasteride reduces some effects.

Some prostate cancers have gene changes that may affect treatment with certain drugs.

A specific gene mutation causes different hair defects in Indian monilethrix families.

SARS-CoV-2 may worsen IPF due to shared genes and pathways, suggesting potential drug targets.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

New SRD5A2 variants may disrupt protein function, aiding diagnosis and treatment of related disorders.

Metformin increases FSH levels in PCOS, and KISS1 gene variations may influence PCOS development.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

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

The HSD3B1 variant increases hair loss risk in overweight women with PCOS.

STK11 gene polymorphism does not predict metformin response in PCOS.

MCHR2 gene duplications may be linked to alopecia areata.

Certain genetic variants linked to immune response increase the risk of alopecia areata in Taiwanese people.

New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

The testes significantly contribute to vitamin D metabolism and may affect male reproductive health and conditions like hair loss.

Certain SPINK5 gene mutations are common in Israeli families with Comèl-Netherton syndrome.

Tunisian children with hereditary vitamin D-resistant rickets showed improvement with calcium treatment, and new genetic mutations were identified.

Different types of PPARγ are found in varying amounts in human skin and its parts, which could affect how skin treatments work.