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DORN1 receptor affects eATP-induced stomatal changes but not eADP in Arabidopsis thaliana.

AKR1D1 controls glucocorticoid levels and receptor activity in liver cells.

AH-001 could be a safer and more effective treatment for hair loss.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

CSLD1 suppresses rice root hair growth with NH4+ and regulates AMT1;2 expression.

Scientists found a gene in mice that causes early hearing loss.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

Early diagnosis and genetic counseling are crucial for managing adrenoleukodystrophy.

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.

A specific gene change in APCDD1 increases the risk of hair loss.

A mutation in the Soat1 gene causes hair structure defects and other health issues in AKR/J mice.

A genetic mutation in a specific gene causes a salt-wasting condition in a Pakistani girl and her family.

Certain genetic variants impair enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

Allopregnanolone is needed for certain brain processing issues caused by D1 dopamine receptor activation.

The condition is linked to chromosome 12, but no mutations were found in the known genes.

Certain gene variations may increase the risk and severity of alopecia areata.

Mutations in the ABCB6 gene cause Dyschromatosis Universalis Hereditaria.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

The Arabidopsis rhd2 mutant is more sensitive to drought because of changes in cell membrane proteins and cell structure.

A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.

Researchers found a new mutation causing total hair loss from birth.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

A certain gene variation can affect protein production and is linked to male pattern baldness.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

The structure of SRD5A reveals how it reduces steroids, aiding drug design for related health conditions.