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Mutations in the NR3C1 gene cause a rare condition that affects hormone signaling and can lead to various symptoms, with dexamethasone as a treatment option.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

Increasing EGR1 levels makes hair root cells grow faster.

Removing the VDR gene in skin cells reduces their growth and affects hair-related genes.

Vitamin D receptor is crucial for skin wound healing.

Different people show different symptoms for genetic diseases because of how sensitive their bodies are to small changes in important factors.

The research found that male pattern hair loss is mostly genetic and involves hair thinning due to hormonal effects and changes in gene expression.

PPAR agonists show promise for skin conditions but need more research before being a main treatment.

Vitamin D receptor can control the hairless gene linked to hair loss even without vitamin D.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

Lymphatic vessels are essential for health and can be targeted to treat various diseases.

Mutations in the glucocorticoid receptor gene cause reduced sensitivity to glucocorticoids and may lead to poor response to treatment.

Protein microarrays are highly sensitive tools useful for disease diagnosis and studying proteins.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Skin cell types develop when specific genes are turned on by removing certain chemical tags from DNA.

Some viruses can cause cancer by changing cell processes and avoiding the immune system; vaccines and targeted treatments help reduce these cancers.

The E2 protein affects gene activity in hair follicles of mice.

AP-2α and AP-2β proteins are essential for healthy adult skin and hair.

TGF-β is crucial for tissue repair and can cause diseases if not properly regulated.

Hormones and metabolism play a complex role in prostate enlargement, and more research is needed to improve diagnosis and treatment.

A rare genetic mutation found in an Indian family can be detected through prenatal screening.

Histone modification is key in treating chronic inflammatory skin diseases.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

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

Certain interactions help prepare the androgen receptor for pairing and activation, which is important for its role in development and disease.

Scientists successfully created and analyzed the structure of a part of the human androgen receptor with specific modulators and a peptide to understand how it binds differently in various tissues.

Pantothenic acid helps mink hair follicles grow by affecting certain cell signals.

The enzymes Tet2 and Tet3 are important for skin cell development and hair growth.

Four-amino acid part makes enzyme sensitive to finasteride.

Epigenetic mechanisms control skin development by regulating gene expression.