Search

everythinglearnresearchcommunity

for

Search:↓

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

The transition from growth to regression in Cashmere goat hair follicles involves changes in expression of genes related to keratin and cell differentiation.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

Genetically modified sheep with more β-catenin grew more wool without changing the wool's length or thickness.

Keratin protein production in cells is controlled by a complex system that changes with cell type, health, and conditions like injury or cancer.

KRTAP6 genes affect wool quality in sheep.

Future hair loss treatments should aim to extend hair growth, reactivate resting follicles, reverse shrinkage, and possibly create new follicles, with gene therapy showing promise.

Feather patterns form through genetic and epigenetic controls, with cells self-organizing into periodic patterns.

Giving a special protein to dogs with a certain genetic disease improved their symptoms but didn't help with hair growth.

A WNT10A gene mutation leads to ectodermal dysplasia by disrupting cell growth and differentiation.

Researchers identified genes linked to coat color, body size, cashmere production, and high altitude adaptation in goats.

Certain signals and genes play a key role in hair growth and regeneration, and understanding these could lead to new treatments for skin regeneration.

Hair diversity is influenced by complex genetics and environmental factors, requiring more research for practical solutions.

The research concluded that selection significantly shaped the genetic variation of the X chromosome, with certain regions affected by past selective events.

Hair disorders are caused by a complex mix of biology, genetics, hormones, and environmental factors, affecting hair growth and leading to conditions like alopecia.

The conclusion is that genetic testing is important for diagnosing and treating various genetic hair disorders.

lncRNA XLOC_008679 and gene KRT35 affect cashmere fineness in goats.

Genetic changes in mice help understand skin and hair disorders, aiding treatment development for acne and hair loss.

Researchers identified specific genes that are important for mouse skin cell development and healing.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

Genes related to pigmentation, body rhythms, and behavior change during hares' seasonal coat color transition, with a common genetic mechanism in two hare species.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

The study found that giant pandas have more melanin in black hair follicles than white, with gene expression differences that could affect hair color and skin health.

Genes related to calcium signaling and lipid metabolism are important for curly hair in Mangalitza pigs.

A specific genetic deletion in goats affects cashmere yield and thickness.

BMP signaling controls hair follicle size and cell growth by affecting cell cycle genes.

The study found key genes and pathways involved in cashmere goat hair growth stages.

The most different genetic segment between Africans and East Asians is the EDA2R/AR region, with two main types influenced by population changes and natural selection, and linked to baldness.

miR-31 regulates hair growth by controlling gene expression in hair follicles.