Search

everythinglearnresearchcommunity

for

Search:↓

Gene therapy, especially using atoh1, shows promise for creating functional sensory hair cells in the inner ear, but dosing and side effects need to be managed for clinical application.

61 functional keratin genes were identified in dogs and horses, leading to updated gene annotations.

Activin A increases inner ear hair cell development, while follistatin decreases it.

The AR gene is linked to male-pattern baldness, TNFSF4 to heart disease, SLC19A3 to BBGD, MCT8 to a syndrome, and segmental duplications to genetic variation.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

Androgen receptors in the brain affect metabolism and reproduction differently in males and females, and may help manage PCOS symptoms in females.

Injecting specific oligonucleotides can change hair growth and structure by altering a gene.

μ-opiate receptors in skin cells may affect skin health and healing.

Keratin gene regulation was emerging, with a key transcription factor found to influence hair growth and gene expression.

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

Ornithine decarboxylase is crucial for hair growth regulation in mice.

The androgen receptor gene doesn't help identify women likely to have female pattern hair loss.

Scientists found new and known long non-coding RNAs in mouse hair follicle stem cells that may be important for stem cell function and could be targets for cancer treatment.

Key genes and RNA networks regulate hair growth and follicle density in Rex rabbits.

Shorter GGN repeats in the androgen receptor gene are linked to androgenetic alopecia.

C57BL/6 mice and SD rats have different sweat gland and hair follicle patterns, useful for skin research.

CD8A and FOXD2-AS1 may be key for diagnosing and treating alopecia areata.

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

The study concludes that a genetic mutation in TFM mice leads to reduced androgen receptor activity, affecting the body's response to male hormones.

A specific DNA region is crucial for Foxn1 gene expression in thymus cells but not in hair follicles.

LHX2 and SOX9 identify unique hair follicle cell groups, crucial for hair maintenance.

Meis2 is essential for touch sensation and proper nerve connection to touch receptors in certain skin areas of mice.

GFRα2 is essential for controlling neuron size but not for target innervation in certain sensory neurons.

Disrupting the Hars2 gene in mice causes hearing loss due to mitochondrial problems and hair cell damage.

The gene LRRC15 is more active in balding areas of the scalp compared to non-balding areas.

FGFR2 signaling controls Merkel cell formation in different skin regions.

The osteopontin gene is active in a specific part of rat hair follicles during a certain hair growth phase and might affect hair cycle and diseases.

MOF controls key genes for skin development by regulating mitochondrial and ciliary functions.