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A specific protein complex increases the activity of a plant enzyme, but this action is not required for plant root hair growth.

AR polyglycine repeat doesn't cause baldness.

Mutant CDP/Cux protein causes hair defects and reduced male fertility in mice.

Specific RNA patterns are linked to alopecia areata.

Rapamycin treatment helps with mitochondrial disease by reducing PKC levels.

Deleting the MAD2L1 gene in mice led to rapid tumor growth despite chromosomal instability.

Certain variations of the HDAC9 gene can increase or decrease stroke risk in the Chinese population.

Esrp1 is important for skin health by helping form and maintain the skin barrier.

Certain gene variations are found in people with polycystic ovary syndrome.

Researchers found that certain RNA molecules might play a role in the growth of Cashmere goat hair.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

Ptprq has multiple forms that change during inner ear development.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

A boy with a new NR5A1 gene mutation has a sex development disorder without affecting his adrenal glands.

Long noncoding RNAs help regulate hair follicle density in rabbits.

Four circRNAs were found to be significantly different in cashmere goat skin, affecting cashmere fineness.

The hairless gene in Kunming mice is important for hair and skin, and shows genetic variations.

The genes KRT25 and SP6 affect curly hair in horses, with KRT25 also causing hair loss. If both genes are mutated, the horse gets curly hair and hair loss. KRT25 can hide the effect of SP6.

New treatments for hair growth and psoriasis may be possible, and gene differences could affect baldness and the severity of skin conditions.

The study concluded that specific proteins are necessary to maintain the structure that holds epithelial cells tightly together.

Long noncoding RNAs may help understand rabbit hair follicle density.

Alopecia areata is likely an autoimmune disease with unclear triggers, involving various immune cells and molecules, and currently has no cure.

EDA2R gene linked to hair loss.

People with X-linked hypohidrotic ectodermal dysplasia have no sweat ducts and less, thinner hair.

Keratin 33A is a key protein in goat winter coats, especially in high-producing breeds.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

Genetic variations affect dutasteride treatment response for male pattern hair loss.

The Asiatic lion has very low genetic diversity and unique genetic traits, highlighting the need for its conservation.

The KRTAP7-1 gene is very similar across different cattle and yak breeds and likely plays a role in hair strength and shape.

C4BPA protein may link acne severity and insulin resistance.