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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.

Mutations in the DSG4 gene cause fragile, sparse hair in humans, mice, and rats.

Genetic variants in PDE6H and LPAR6 cause vision impairment and hair loss in two Pakistani brothers.

Eating a high-fat fish oil diet caused mice to lose hair due to a specific immune cell activity in the skin linked to a protein called E-FABP.

Two mutations in KRT74 and EDAR genes cause sheep to have finer wool.

Keeping β-catenin levels high in mammary cells disrupts their development and branching.

Softer hydrogels help wounds heal better with less scarring.

Hairlessness in mammals is caused by combined changes in genes and regulatory regions.

Hairless mammals evolved quickly in both gene and non-gene areas related to skin and hair.

A new mutation in the Connexin 26 gene was found in a patient with KID syndrome, expanding the known disorders linked to this gene.

Mutations in three genes cause Uncombable Hair Syndrome, leading to frizzy hair that can't be combed flat.

Frizzled receptors are essential for various body development processes and maintaining certain body functions.

Large-scale fibronectin nanofibers help heal wounds and repair tissue in a skin model of a mouse.

Disabling the FGF5 gene in sheep leads to longer wool.

A specific enzyme is crucial for the bean plant's relationship with certain beneficial soil bacteria and fungi.

A protein called IL-36γ causes skin side effects from certain cancer treatments when combined with a common skin bacteria.

Chinese domestic goats have unique genetic traits due to domestication and geographic isolation.

The supplement helps improve hair growth and reduce hair shedding.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

A specific gene mutation causes congenital hair loss.

Immune cells in Hidradenitis suppurativa become more inflammatory and may be important for treatment targets.

Ichthyosis with confetti is a genetic skin disorder with consistent ectodermal malformations and various KRT10 gene mutations.

PPARγ is essential for maintaining healthy skin, controlling inflammation, and ensuring proper skin barrier function.

A specific gene mutation causes long hair in Angora rabbits.

Low-coverage sequencing is a cost-effective way to find genetic factors affecting rabbit wool traits.

A new therapy for a skin blistering condition has not been developed yet.

A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.

Three specific genetic variants cause severe skin issues in children with EBS, highlighting the need for early genetic screening.

A new method using a microfluidic device can prepare hair follicle germs efficiently for potential use in hair loss treatments.

A specific hair protein variant increases the spread of breast cancer and is linked to worse survival rates.