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Using a combination of specific cell cycle regulators is better for safely keeping hair root cells alive indefinitely compared to cancer-related methods.

A 15-year-old girl with no menstrual period was diagnosed with a genetic condition that makes her body unable to respond to male hormones, leading to female characteristics despite having male genetic makeup.

A complex X chromosome rearrangement can increase the risk of multiple autoimmune diseases.

Beta-sitosterol has potential health benefits but needs more research to fully understand its effects and improve its use in treatments.

Researchers found 63 genes linked to male-pattern baldness, which could help in understanding its biology and developing new treatments.

ESR2 gene variations may be linked to female pattern hair loss.

DNA methylation and long non-coding RNAs are key in controlling hair growth in Cashmere goats.

Found different proteins in balding and non-balding cells, giving insight into hair loss causes.

Gene differences may affect baldness treatment response in Korean men.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

Inherited color dilution in Rex rabbits is linked to DNA methylation changes in hair follicles.

Two specific hair keratin genes are active during hair growth and decline as hair transitions to rest.

Cashmere and milk goats have different hair growth cycles and gene expressions, which could help improve wool production.

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.

The document concludes that mouse models are crucial for studying hair biology and that all mutant mice may have hair growth abnormalities that require detailed analysis to identify.

New genetic locations explain much of hair color variation in Europeans.

Certain genes in Iranian sheep are linked to wool production and heat adaptation.

Inherited color dilution in rabbits is linked to DNA methylation changes.

Rare genetic variants in five specific genes are linked to male-pattern hair loss but only account for a small part of the risk.

New single-cell analysis techniques are improving our understanding of stem cells and could help in treating diseases.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

Key genes and pathways involved in thyroid eye disease were identified, aiding potential treatment and diagnosis.

Hair microscopy is useful for diagnosing hair disorders, but clear definitions are needed for accurate genetic analysis.

Sansevieria trifasciata Prain shows promise for treating hair loss by inhibiting androgen receptors.

IFN-γ and IL-2 are important for T cell activation in hair loss in mice.

Deleting the MAD2L1 gene in mice led to rapid tumor growth despite chromosomal instability.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

The 190-kbp domain contains all human type I hair keratin genes, showing their organization and evolution.

S100A3 protein is crucial for hair shaft formation in mice.