Search

everythinglearnresearchcommunity

for

Search:↓

Type 3 5α-reductase is more common and finasteride and dutasteride strongly inhibit it.

Two enzymes regulate androgen receptor activity, affecting treatments for androgen insufficiency and benign prostatic hyperplasia.

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

New genes and pathways are important for testosterone production and male sexual development.

KRTAP genes evolved early in mammals, leading to diverse hair traits.

ICP5249 helps hair grow by activating a specific cell pathway.

The study found that women with hyperandrogenic PCOS have higher levels of AKT1 and AKT2 proteins in their cells, which may lead to cell dysfunction.

MAP-2 is crucial for the structure of hair follicles and nails.

Increasing TSPO in the brain reduces anxiety and depression.

Human liver cells stick to hair protein materials mainly through the liver's asialoglycoprotein receptor.

TAp63 and NRF2 work together to manage oxidative stress, preventing premature aging and aiding skin functions.

PRDX5 enzyme may contribute to alopecia areata by affecting oxidative stress and autoimmunity.

The hairless gene is crucial for hair health, and its mutations cause hair loss.

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

Ruxolitinib may effectively treat APS-1 by reducing harmful immune responses.

ODC1 gene mutations cause a neurodevelopmental disorder with large head size, hair loss, and facial abnormalities.

RPGRIP1L helps skin cells stick together by blocking PKCβII, which can prevent skin blistering like in pemphigus.

Profilin1 speeds up wound healing.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

Mitochondrial problems in tooth cells lead to bad enamel and dentin development in mice.

MitoQ helps protect hair cells from damage in hair loss by boosting a protective enzyme.

Genetic variation in the KRTAP15-1 gene affects wool yield in sheep.

The new model helps understand and develop treatments for genetic skin disorders like AEC.

Removing the ATR gene in adult mice causes rapid aging and stem cell loss.

Scientists found a new type of skin cell that could help with skin repair and these cells work better with a certain protein.

PRSS35 enzyme may help start skin tumors and could be a target for cancer treatment.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.

ALDOA levels drop in hair cells during hair loss.