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

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

ROOT HAIR SPECIFIC 10 (RHS10) reduces the length of root hairs in Arabidopsis plants.

A special microbe helps plants absorb rock phosphate by growing on their root hairs.

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

Blocking the FGF5 gene in sheep leads to more fine wool and active hair follicles due to changes in certain cell signaling pathways.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

Researchers found a new mutation causing total hair loss from birth.

The study concluded that testing hormone levels after stimulation is not reliable for identifying carriers of 21-hydroxylase deficiency; genetic testing is necessary.

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

A new gene, mrp4, is found in mice and may play a unique role in hair follicle development in tails and ears.

A gene in Sebekia benihana, CYP-sb21, is needed for a specific reaction on the drug Cyclosporine A, which could be important for hair growth without affecting the immune system.

Scientists made stem cells that can grow hair by adding three specific factors to them.

SIPHL1 from tomato enhances plants' response to low phosphate levels.

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

Removing anthrax toxin receptor 1 in pigs prevents Senecavirus A infection and causes a rare disease similar to GAPO syndrome.

SOX9 helps determine stem cell roles by interacting with DNA and proteins that control gene activity.

Pigs without the Hairless gene showed skin and thymus changes, useful for studying human hair disorders.

Stem cells help remove dead cells to keep tissues healthy by balancing cell replacement and clearance.

Certain cells in the adult mouse ear come from cranial neural crest cells, but muscle and hair cells do not.

Scientists can now create skin with hair by reprogramming cells in wounds.

The gene Tfap2b is essential for creating a type of stem cell in zebrafish that can become different pigment cells.

The HoxC gene cluster and its enhancers are essential for developing hair and nails in mammals.

The document summarizes medical findings on topics like heart rhythm treatment, sleep apnea therapy, and various health conditions and treatments.

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

Keratin 15 expression in skin cells is regulated by two mechanisms involving PKC/AP-1 and FOXM1.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

DNMT1 helps turn hair follicle stem cells into fat cells by blocking a specific microRNA.

Different signals work together to change gene activity and guide hair follicle stem cells to become specific cell types.