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Deleting the p63 gene in certain cells causes problems in thymus development and severe hair loss in mice.

Researchers found genes and genetic variants linked to sheep wool and skin wrinkles.

The study found that giant pandas have more melanin in black hair follicles than white, with gene expression differences that could affect hair color and skin health.

DNA methylation changes are linked to hair growth cycles in goats.

Anti-acne medications may work by reducing the activity of a protein involved in acne development.

Blood vessels and specific genes help turn cartilage into bone when bones heal.

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

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

Targeting FGFR-1 with antisense oligonucleotides may help treat baldness by increasing hair follicle activity.

ECM1-modified stem cells can effectively treat liver cirrhosis.

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.

Chicken feather gene mutation helps understand human hair disorders.

Scientists found the best time to transplant human stem cells for hair growth is between days 16-18 when they have the right markers and growth potential.

The ZIP7 gene helps control zinc levels in cells by moving zinc from the Golgi apparatus to the cytoplasm.

The AUTS2 gene is linked to neurological disorders and may affect human brain development and cognition.

Bmpr2 and Acvr2a receptors are crucial for hair retention and color.

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

A specific RNA modification in cashmere goats helps activate hair growth-related stem cells.

The new anti-acne treatment HA-P5 effectively reduces acne by targeting two key receptors and avoids an enzyme that can hinder treatment.

Human skin can be reconnected to nerves using stem cells, which may help with skin health and healing.

Studying premature aging syndromes helps understand human aging and suggests potential treatments.

Riboflavin 5′-phosphate (FMN) shows potential for treating androgen-related conditions but may be limited in treating prostate cancer.

Bimatoprost is effective for growing longer, thicker, and darker eyelashes.

Congenital Adrenal Hyperplasia is a rare inherited disease causing hormone imbalances, affecting growth, fertility, and heart health, diagnosed through blood tests and treated with medication and lifestyle changes.

The VEGF +405G allele may increase the risk of PCOS in South Indian women.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

PNKP is essential for keeping adult mouse progenitor cells healthy and growing normally.

Certain mutations in the H6PD gene cause Cortisone Reductase Deficiency by affecting hormone production.

Women with nonclassical congenital adrenal hyperplasia may have a higher risk of fertility issues and miscarriages, and should get genetic counseling.

Activating TLR9 helps heal wounds and regrow hair by using specific immune cells.