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The nature of the side chain in RU 58841 derivatives greatly affects its AR affinity, with the N-(iodopropenyl) derivative 13 showing the highest AR binding affinity, suggesting its potential for developing high-affinity radioiodinated AR radioligands.

The HIF-2α/ARNT complex is important for hair follicle development by controlling cell growth.

FP-1 is a key protein in rat hair growth, active only during the growth phase.

Runx1 helps control the KAP5 gene in human hair follicles.

A new AIRE gene mutation causes rare autoimmune symptoms in a Lebanese boy.

BcFLA1 protein is crucial for root hair growth in response to low phosphate in Brassica carinata.

17β-estradiol boosts APE1/Ref-1 secretion in cells and mice via a calcium-dependent pathway.

Mutations in β1 integrins cause embryonic death but have milder effects on skin.

Human keratinocytes do not naturally respond to androgens.

Vitamin D receptor can control the hairless gene linked to hair loss even without vitamin D.

ROOT HAIR SPECIFIC 10 (RHS10) reduces the length of root hairs in Arabidopsis plants.

The L457(3.43)R mutation in the human lutropin receptor causes increased activity and hormone insensitivity, leading to precocious puberty.

PLA2R1 overexpression harms kidney cells by stopping their growth cycle.

APS-1 in Italy shows diverse AIRE mutations and various autoimmune issues.

The Agouti gene influences pigmentation and may have a developmental role in deer mice.

The research found how GPCR Class A Rhodopsin receptors are related and suggested possible substances they interact with.

TRPA1 is crucial for mechanical sensitivity in skin sensory neurons.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

A mutation in the iRhom2 gene causes hairless mice due to abnormal hair follicle development.

FER and TOR signaling help root hair growth in low temperature and low nitrate conditions.

Stress can cause a type of hair loss in mice lacking the CCHCR1 gene.

The LncRNA AC010789.1 slows down hair loss by promoting hair follicle growth and interacting with miR-21 and the Wnt/β-catenin pathway.

FERONIA is crucial for plant growth, pollen tube reception, and sugar signaling.

The mK6irs1/Krt2-6g gene likely causes wavy hair in mice.

Androgen receptor activity blocks Wnt/β-catenin signaling, affecting hair growth and skin cell balance.

Activated ras can protect kidney cells from a certain substance that causes cell death.

A specific mutation in PA-PLA1α causes abnormal hair growth.