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The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

Adult skin cells can be used to create new hair in a lab.

Poor maternal nutrition can lead to fewer wool follicles in Chinese Merino sheep.

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

A man with a rare skin condition and a new gene mutation developed high calcium levels due to his treatment.

The study found specific proteins that could mark different growth stages of cashmere goat hair and may help improve cashmere production.

Scientists created a 3D skin model to study a chronic skin disease and test treatments.

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

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.

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

Proteomics combined with other technologies can lead to a better understanding of skin diseases.

Hairless protein affects hair follicle structure by regulating the Dlx3 gene.

Topical minoxidil may help treat a rare genetic hair condition with no fully effective treatments yet.

Genes related to keratin, skin cell differentiation, and immune functions are key in hedgehog skin and spine development.

lncRNA XLOC_008679 and gene KRT35 affect cashmere fineness in goats.

Li2CO3 improved skin disease in a mouse model of Focal Dermal Hypoplasia without toxicity.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

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

Hair loss in certain mice is linked to changes in keratin-related genes.

Keratin 17 is linked to various diseases, including cancer and skin conditions, and may be a target for diagnosis and treatment.

Blood cells turned into stem cells can become skin cells similar to normal ones, potentially helping in skin therapies.

DermaCult™ Keratinocyte Expansion Medium allows human skin cells to grow longer while keeping their ability to develop properly.

KRT14 gene variants cause dermatopathia pigmentosa reticularis, affecting nails, teeth, and hair.

K42 and K124 keratins are only found in horse hoof lamellae.

Epidermolytic ichthyosis can be inherited in a semidominant way with mild symptoms in carriers.

Dorper sheep's wool shedding is linked to specific genes and pathways, which may help understand human hair growth.

Steatocystoma multiplex causes recurring skin cysts and needs early recognition for better management.

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

Sebaceous glands can heal and regenerate after injury using their own stem cells and help from hair follicle cells.

Keratin proteins are crucial for hair growth in cashmere goats.