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The osteopontin gene is active in a specific part of rat hair follicles during a certain hair growth phase and might affect hair cycle and diseases.

ERβ has potential in treating prostate cancer and neurodegenerative diseases, but human studies are needed before clinical use.

Finasteride affects SRD5A2 gene pattern, possibly causing lasting side effects.

Guasha changed rat skin appearance and blood vessels temporarily without affecting certain nerve proteins or fiber structure.

A new gene mutation causes insulin resistance in a girl and her mother.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

Fadrozole and finasteride change gene expression related to sex hormones and thyroid hormones in frog larvae development.

Erbium glass laser treatment may help with skin remodeling, reduce inflammation, and improve skin cell maturation.

Researchers found an RNA transcript that might help control a growth factor linked to tumor development.

Blood tests can help understand the genetic differences in people with alopecia areata, including how severe it is and if it's inherited.

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

Researchers found a gene in hamsters that responds to male hormones and may be indirectly controlled by them.

Ishige sinicola extract helps bone-building cells grow and mature, which could aid in treating osteoporosis.

Allopregnanolone increases growth and changes gene activity in human brain cancer cells.

Vitamin D boosts a specific gene activity in kidney cells that could improve heart and kidney function.

Thyroid hormones and androgens affect gene expression in frog reproductive organs differently between males and females.

A new mutation in the AGPAT2 gene causes severe fat tissue loss and related health issues by reducing the protein's levels.

Genetic screening can help diagnose and manage infertility in Slovenian couples.

Estrogen Receptor ß (ERß) is the main hormone controller in human skin and hair follicles, not Estrogen Receptor α (ERα) or the Androgen Receptor (AR).

Understanding gene expression in hair follicles can reveal insights into hair growth and disorders.

K_ATP channel gene mutations are linked to heart diseases, but more research is needed to understand the connection and treatment potential.

Mutations in the PTPRQ gene cause significant balance issues in mice due to hair bundle defects in the inner ear.

New therapies for Birt–Hogg–Dubé syndrome are being developed based on understanding the FLCN gene's role.

A gene in Arabidopsis thaliana, AtPRPL1, affects root hair length but not cell wall composition.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

Activating ER-β, not ER-α, improves skin cell growth and wound healing.

FoxN1 gene is essential for proper thymus structure and preventing hair loss.

WNT7A gene expression is higher in early stages of androgenetic alopecia, showing the role of WNT pathway, apoptosis, and inflammation in the disorder.

Male yak hair growth is influenced by DHT synthesis, which is promoted by 5α-red1 and AR during growth phases, while E2 may inhibit growth through ERα.

Keratin protein production in cells is controlled by a complex system that changes with cell type, health, and conditions like injury or cancer.