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Vitamin D receptor is crucial for starting hair growth after birth.

Nonclassic adrenal hyperplasia is a genetic condition that can cause early puberty and fertility problems, treated with specific steroids.

Prolactin slows down hair growth in mice.

K16 can partially replace K14 but causes hair loss and skin issues.

HIV can cause unusual and severe skin problems that are hard to treat.

New treatments for Hepatitis C show promise but need more research to confirm their safety and effectiveness for clinical use.

Parathyroid hormone-related protein helps control hair growth phases in mice.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

A gene called HDAC9 might be a new factor in male-pattern baldness.

The gene for slick hair in Senepol cattle is located on chromosome 20 and may involve the SRD5A2 gene.

Mice with human skin protein K8 had more skin problems and cancer.

A 3-month stay in space causes skin thinning, disrupts hair growth, and changes muscle-related genes in mice.

DNA variants can predict male pattern baldness, with higher risk scores increasing baldness likelihood.

The document concludes that future heart disease research should account for sex-specific differences to improve diagnosis, treatment, and outcomes.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

Certain skin conditions may indicate or increase the risk of Parkinson's disease.

The research suggests that the global distribution of PCOS is likely due to historical human migration and that genes affecting PCOS may have different impacts on males and females.

Genes play a significant role in male-pattern baldness, and understanding them could lead to new treatments and insights into related health issues.

Some natural compounds may help overcome drug resistance in certain cancers, but more research is needed.

A gene variation is linked to hair thickness in Asians.

α3β1-integrin is crucial for maintaining normal hair follicle shape and function but not needed for the development of the surrounding skin.

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

CYLD mutations cause a variety of skin tumors with symptoms starting around age 16, and treatments are currently limited.

Genetic variations affecting skin structure play a key role in severe acne.

Hoxc genes control hair growth through Wnt signaling.

CLE40 and CRN/CLV2 pathways have opposite effects on root growth in Arabidopsis.

The gene KAP22-1 affects wool yield and fiber shape in sheep.

RACB in barley is crucial for cell polarity and nucleus positioning, aiding fungal infection.

G allele of AR Stul polymorphism linked to higher hair loss risk, especially in white people.

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.