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

FGF-5 promotes Cashmere goat hair growth by increasing keratin genes and reducing certain LncRNA and target genes.

Scientists developed tools to observe hair regeneration in real time and assess skin health, using glowing mice and light-controlled genes.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

Certain mouse strains develop a skin condition similar to a human hair loss disease due to genetic defects.

Woodhouse-Sakati syndrome often causes sexual development issues, hair loss, learning disabilities, deafness, muscle contractions, limb pain, and diabetes.

ARL15 is important for fat cell development and the release of the hormone adiponectin.

The study concludes that mutations in the AEBP1 gene can cause a form of Ehlers-Danlos syndrome and should be considered in diagnosis.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

A woman with a rare hormone resistance condition also had missing teeth and hair loss, which might be new symptoms of her genetic disorder.

The research provides insights into hair follicle growth in forest musk deer by identifying key genes and pathways involved.

Some lesser-known causes of PCOS include autoimmune issues, genetic mutations, and changes in the body's microbiome.

A man with kidney tumors and lung cysts was diagnosed with Birt–Hogg–Dubé syndrome and treated successfully, with genetic testing confirming the diagnosis.

Men are more likely to have severe COVID-19 cases and fatalities than women due to factors like lifestyle, aging, and biological differences.

Fat cells in the skin help start healing and form important repair cells after injury.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

The research identified various cell types in mouse and human teeth, which could help in developing dental regenerative treatments.

Mutations in the PADI3 gene are linked to a higher risk of scarring hair loss in women of African descent.

Genetics and hormones play a role in male and female hair loss, but more research is needed to fully understand it.

Exosomes from dermal papilla cells help hair growth by making hair follicle stem cells multiply and change.

Acne is caused by genetics, diet, hormones, and bacteria, with treatments not yet curative.

CLE40 and CRN/CLV2 pathways have opposite effects on root growth in Arabidopsis.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

A male with aromatase deficiency improved bone health with estradiol treatment.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

The research suggests that Tourette syndrome is linked to both brain signaling and immune system pathways.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

A family got a fungal infection from a boy who had contact with rabbits, but they all recovered with treatment.

New treatments for hair loss are showing promise due to better understanding of genetics and the immune system.

The monkey's hair loss was due to an autoimmune disease, not genetics.