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A new mutation linked to partial Androgen Insensitivity Syndrome and prostate cancer was found in a patient unhappy with their female gender assignment.

SOX9 helps determine stem cell roles by interacting with DNA and proteins that control gene activity.

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

The research identified and described a gene important for hormone conversion in endangered catfish, which varies in activity during different reproductive stages and after hormone treatment.

XMU-MP-1 stops cell growth in a human mini-organ and reduces the effectiveness of the chemotherapy drug paclitaxel.

A deficiency in the TTC7A gene causes immune problems, gut issues, and hair loss.

BST2 is a key marker for hair loss disease alopecia areata.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

Certain genes and pathways are linked to the production of finer and denser wool in Hetian sheep.

The enzyme PST is found in developing human kidneys and helps with detoxification and development.

The CTLA-4 gene polymorphism does not affect polycystic ovarian syndrome.

TTD hair is brittle due to fewer sulfur amino acids and unstable disulfide bonds.

Serotonin helps wounds heal faster.

Early involution in Hirosaki hairless rats' mammary glands is linked to a unique modification of STAT5A.

Tiger tail banding and hair abnormalities are reliable indicators for diagnosing trichothiodystrophy.

CRAC channels are crucial for the development and function of specialized immune cells, preventing severe inflammation and autoimmune diseases.

MC-DNA vector-based gene therapy can temporarily treat CBS deficiency in mice.

The UHS promoter is specific to mouse hair follicles.

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

Smad4 is crucial for muscle repair, especially in aging, by promoting cell growth over differentiation.

Certain gene variations may increase the risk of PCOS in South Indian women.

The protein EZH2 blocks microRNA-22, increasing STK40 protein, which helps hair follicle stem cells change and grow hair.

p63 is essential for controlling epithelial stem cells and tissue health.

GLI1 might protect against the start of skin cancer and is not linked to cancer severity.

A mutation in the KRT74 gene causes woolly hair by affecting hair texture.

Researchers found a gene mutation responsible for a rare hair loss condition.

Polycomb Repressive Complex 1 is crucial for keeping stem cells stable and maintaining healthy adult tissues.

Loss of the p53 gene alone causes tumors, and losing both p53 and Rb genes speeds up aggressive skin cancer.

A mutation in the KRT74 gene causes woolly hair by affecting hair texture.