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Mutations in the LSS gene cause a rare type of hereditary hair loss.

The length of the CAG repeat in the androgen receptor gene affects the risk and progression of prostate cancer, BPH, infertility, and undermasculinized genitalia.

CGRP may help protect hair follicles from immune system attacks, potentially slowing hair loss.

Androgen receptor activity blocks Wnt/β-catenin signaling, affecting hair growth and skin cell balance.

Mutations in the PTPRQ gene cause significant balance issues in mice due to hair bundle defects in the inner ear.

New therapies for Birt–Hogg–Dubé syndrome are being developed based on understanding the FLCN gene's role.

A gene in Arabidopsis thaliana, AtPRPL1, affects root hair length but not cell wall composition.

A specific protein complex increases the activity of a plant enzyme, but this action is not required for plant root hair growth.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

Mice without the Sp6 gene have problems developing several body parts, including hair, teeth, limbs, and lungs.

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

Human keratinocytes do not naturally respond to androgens.

Testing for CAG repeat polymorphism in the androgen receptor gene is not currently recommended for managing hypogonadism.

Proper control of β-catenin activity is crucial for development and preventing diseases like cancer.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

Mutations in the androgen receptor gene cause Androgen Insensitivity Syndrome, affecting sexual development.

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

FoxN1 gene is essential for proper thymus structure and preventing hair loss.

The study concludes that mutations in the AEBP1 gene can cause a form of Ehlers-Danlos syndrome and should be considered in diagnosis.

The gene Msx2 is crucial for hair follicle regeneration during wound healing.

A gene called Gk5 controls lipid production in the skin and affects hair growth.

A boy's growth and immune problems were caused by a new mutation in the STAT5B gene.

A new mutation in the HR gene causes hair loss in a specific family.

High mTORC1 activity slows hair growth and causes it to lose color.

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

The gene NM_026333 slows down aging by affecting the NCX1 pathway and could be targeted for anti-aging treatments.

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

The compounds tested could potentially treat hair loss and alopecia.

DHT inhibition may increase spinal bone growth in ankylosing spondylitis.

WNT7A gene expression is higher in early stages of androgenetic alopecia, showing the role of WNT pathway, apoptosis, and inflammation in the disorder.