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

Protein tyrosine kinases are key in male pattern baldness, affecting skin structure, hair growth, and immune responses.

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.

In situ DNA labeling in hair can help predict forensic DNA analysis success.

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

Small amounts of DNA can be found in the hair shaft, especially near the root, but it decreases with hair treatments and washing.

The document explains how to create detailed biological pathways using genomic data and tools, with examples of hair and breast development.

Hair follicle stem cells change states with age, affecting hair growth and aging.

Albumin and prednisone improved symptoms in a woman with Cronkhite-Canada syndrome, revealing potential genetic causes.

The study found that the hair loss condition in Cesky Fousek dogs is influenced by multiple genes affecting skin and muscle structure, fat metabolism, and immunity.

Personalized treatments for hair loss are becoming more effective by using genetic information.

The study concluded that the arachidonic acid pathway and the protein KRT79 play a role in determining the fineness of cashmere.

Certain gene variations are linked to the thickness of cashmere goat hair.

Certain genetic variants in ERN1, TACR3, and SPPL2C are linked to when Alzheimer's disease starts.

The scalp microbiome is more diverse and may be more important in hair loss than the gut microbiome.

Key genes crucial for sheep hair follicle development were identified, aiding fine wool breeding and human hair loss research.

Certain variations in the vitamin D receptor gene are linked to an increased risk of polycystic ovary syndrome.

The research found that the molecule lncRNA-H19 helps hair follicle cells grow by affecting certain cell pathways in cashmere goats.

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

Finasteride treatment in rats changed the expression of genes related to psychiatric and neurological functions, and these changes persisted after stopping the drug.

A mother's iron levels early in pregnancy can influence the DNA makeup of her child, potentially affecting the child's health.

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

New method finds genetic links between Type 2 Diabetes and Prostate Cancer not seen before.

Researchers found genes and microRNAs that control curly fleece in Chinese Tan sheep.

The study found key factors in the cause of hidradenitis suppurativa, its link to other diseases, and identified existing drugs that could potentially treat it.

Menopause causes significant changes in the vaginal introitus, but less so in the labia majora, which may lead to symptoms of vaginal atrophy.

Fasting in hens affects thyroid hormones, which regulate feather and hair growth.

mEphA1 receptor tyrosine kinase is important for skin and hair development and may play a role in certain diseases.

Genetic factors could lead to personalized treatments for hair loss.

Combining genetic and physical trait analysis improves diagnosis accuracy for monogenic diabetes.