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Mice lacking Insig proteins had hair growth problems due to cholesterol buildup, but this was fixed by the drug simvastatin.

Jagged-1 in skin Tregs is crucial for timely wound healing by recruiting specific immune cells.

People with Alopecia Areata often have thyroid problems like Hashimoto thyroiditis and hypothyroidism.

Baldness, especially at the front, may lower the risk of testicular cancer by 31%, but its link to prostate cancer is unclear.

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

Melatonin helps wheat plants resist drought by improving their root and root hair growth.

SOX9 helps determine stem cell roles by interacting with DNA and proteins that control gene activity.

Certain inhibitors slow down plant growth by causing early cell specialization without changing the cell development pattern.

Poor maternal nutrition can lead to fewer wool follicles in Chinese Merino sheep.

Certain genetic variations are linked to higher liver enzyme levels in patients treated for chronic hepatitis C with specific drugs.

Filaggrin mutations are linked to atopic dermatitis and help explain how genetics and environment affect the disease.

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

AR gene not major factor in female hair loss; different from male hair loss.

The KRTAP21-1 gene affects wool yield and can help improve wool production.

The androgen receptor gene doesn't affect women with recurrent spontaneous abortions, but having a mutant genotype might protect against it.

LIPH mutations in Japan cause varying degrees of hair loss and woolly hair.

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

No consistent link between genotype and phenotype in 5-α-Reductase type 2 deficiency.

Certain IL-18 gene variations may increase the risk of alopecia areata.

Case-only trees and random forests improve predictions of treatment effects in clinical trials.

A new EDA gene mutation was found in a Chinese family with a specific skin disorder.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

Women with nonclassic congenital adrenal hyperplasia experience more sexual dysfunction and distress.

The article concludes that global standardization in PCOS research is crucial for accurate diagnosis and understanding of the condition.

Androgenetic alopecia is linked to a higher risk of coronary heart disease due to certain genetic factors and high homocysteine levels.

Certain gene variations may increase the risk of hair loss in Egyptians.

Dutasteride and finasteride affect different cell types differently.

PCOS may have evolved as an advantage in past environments with food scarcity.