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

Blocking Prostaglandin D₂ (PGD₂) could help treat hair loss.

CLE40 and CRN/CLV2 pathways have opposite effects on root growth in Arabidopsis.

A specific gene mutation causes a severe skin disorder in a family.

Researchers fixed gene mutations causing a skin disease in stem cells, which then improved skin grafts in mice.

Skin cells can naturally limit the growth of cancerous changes by balancing cell renewal and differentiation.

The balance between cell renewal and differentiation controls the growth of cancerous cells in mouse skin.

PRP can improve hair growth in people with hair loss, but more research is needed.

Over-expression of Sp2 can lead to cancer by preventing proper stem cell differentiation.

G allele of AR Stul polymorphism linked to higher hair loss risk, especially in white people.

Scientists made a sensor that can detect a specific type of RNA related to androgen receptors quickly and accurately.

ARHGEF3 is essential for proper hair follicle development in mice.

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

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

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

GLI2 increases follistatin production in human skin cells.

CCDC22 and CCDC93 are essential for root and root hair growth in Arabidopsis.

Different Hairless isoforms affect Vitamin D receptor activity in hair regulation, with one repressing and the other stimulating it.

Mrp3 helps in wound healing and hair growth.

cgVEGF164 boosts hair follicle growth in mice.

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

Certain gene variations in the Vitamin D Receptor are linked to higher risk of female hair loss.

Certain genetic markers may increase or decrease prostate cancer risk.

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

RNase L hinders hair follicle regeneration by altering immune signals.

Certain genes are linked to wool follicle structure and function, but not hair cycle regulation.

PDRN from trout sperm helps skin and hair regeneration but is costly and complex to produce.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

The KRTAP36-2 gene in sheep affects wool yield.

JW0061 may be a new treatment for hair loss by promoting hair growth through WNT signaling.