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A genetic marker linked to a type of hair loss was found in most patients studied.

The mutated hairless gene causes hair loss by acting as a new type of corepressor affecting thyroid hormone receptors.

Certain gene variations might increase the risk of a hair loss condition in Koreans.

Introducing the OTC gene improved symptoms in mice with OTC deficiency.

Calcium blockers may help prevent hearing loss by protecting hair cells.

Specific gene variants affect wool traits in Chinese Tan sheep.

Different hair fiber development might explain why hair loss severity varies in patients with a specific genetic mutation, and treatments that thicken hair could help.

Keratin 17 is modified by RSK1 in response to growth and stress, affecting skin growth and stress response.

Hairless protein helps control hair growth by regulating vitamin D receptor activity.

Harlequin mutant mice have hair loss due to low AIF protein levels and retroviral element activity.

Genomic profiling for myeloid cancers can find important inherited mutations, but it's challenging when these mutations aren't related to the patient's symptoms.

Uncombable hair is inherited dominantly with complete penetrance.

PRSS35 enzyme may help start skin tumors and could be a target for cancer treatment.

MendelVar is a tool that helps identify important genes by combining GWAS data with Mendelian disease information.

Cats with abnormal hair had DSG4 gene changes causing hair problems.

Overexpressing NSD3 in mice causes breast cancer-like tumors and gland abnormalities.

Researchers found genes that may explain why some pigs grow winter hair, which could help breed cold-resistant pigs.

Trps1 is essential for proper hair follicle development.

Excessive putrescine causes hair loss in transgenic mice by disrupting hair follicle development.

Men with more CAG repeats in the androgen receptor gene and lower testosterone levels may experience more severe COVID-19.

A new mutation caused a rare hair disorder in a Polish girl, not inherited from her family.

The study identified key genes and pathways linked to hair disorders, aiding precision medicine.

Porokeratotic eccrine and hair follicle nevus is a very rare skin disorder possibly caused by a GJB2 gene mutation.

A 4kb fragment of the desmocollin 3 promoter targets gene expression to specific skin and hair follicle areas.

The new Hairless R/J mice model improves imaging for tumor monitoring and cancer therapy evaluation.

Researchers created a mouse model for Cushing's syndrome to study glucocorticoid excess and potential treatments.

Hirosaki hairless rats lack hair due to missing DNA with key keratin genes.

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

Colorectal cancer's ability to spread is due to changes in many genes, not just one.