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The SYP123-VAMP727 complex is important for transporting materials that harden the root hair shank in Arabidopsis.

RXR and RAR proteins in skin may help with cell growth, hair growth, and gland function.

The ACE1 gene variant doesn't affect long-COVID symptoms.

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

MPA increases cancer spread by boosting Eph A2 activity.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

Hair sensitivity to androgens is partly controlled by specific enzyme expressions in different hair areas.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

20(S)-Protopanaxadiol-aglycone may help prevent and treat prostate cancer by reducing androgen receptor activity.

Delta-opioid receptors affect skin cell circadian rhythms, possibly impacting wound healing and cancer.

ETC-159 was safe up to 30 mg, but no tumor shrinkage was seen.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

Certain gene mutations in Japanese people are linked to different types of hair loss, with some causing mild hair thinning and others leading to complete baldness.

Defects in certain proteins cause major heart abnormalities during early development.

Genetic variants at 20p11 increase baldness risk in Chinese Han people.

Not having the gene PLAAT3 leads to fat loss, high insulin resistance, and abnormal fat levels in the blood due to a disruption in fat cell development and function.

A new genetic variant causes BRESHECK syndrome by disrupting cell growth and stress response.

Silencing NtNCED3-2 gene in tobacco reduces drought tolerance and impairs growth.

Introducing the rat OTC gene partially corrected OTC deficiency in mice.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

Type II keratins are uniquely phosphorylated during stress and mitosis, affecting their structure and function.

The study found that variations in hair protein genes are likely due to evolutionary deletions or duplications.

Different versions of the KRTAP6-2 gene in goats can lead to thinner cashmere fibers.

A genetic variant in the KRT25 gene causes tightly curled hair.

Different keratins have unique expression patterns in mouse skin cells.

Rac1 is essential for proper hair structure and color.

IGFBP-rP1 could be a new treatment for a common type of hair loss.

PF-998425 is a new, effective, and non-phototoxic treatment for skin conditions related to androgens.

Enzymes that change arginine to citrulline are important for skin barrier and hair formation, and their malfunction can lead to skin conditions and hair disorders.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.