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PBX1 helps hair stem cells grow and change by turning on certain cell signals and preventing cell death, which may be useful for hair regrowth treatments.

The we/we wal/wal mice have defects in hair growth and skin layer formation, causing hair loss, useful for understanding alopecia.

NBCCS and BFHS might be the same syndrome, helping better identify and manage cases.

The WIF1 gene is crucial for hair growth in Angora rabbits.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

Monilethrix involves multiple genes affecting hair structure, including DSG4 mutations.

Corneal health relies on cell migration and cooperation with the lacrimal gland, not Bmi1+ cells, and Eda gene mutations can cause dry eye disease.

CCL5 is important for the hair growth potential of human dermal papilla cells.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

Mutant MK6a transgenes in mice cause blistering, hair loss, and potential human alopecia.

CREB, a protein that can promote cancer traits, is controlled by β-catenin in skin cancer cells.

Birt–Hogg–Dubé syndrome is a rare genetic condition causing skin lesions, lung cysts, and a higher chance of kidney cancer.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

A rare skin condition in a boy is likely due to a specific genetic mutation pattern.

Genomic profiling for myeloid cancers can find important inherited mutations, but it's challenging when these mutations aren't related to the patient's symptoms.

A new genetic mutation in mice causes permanent hair loss and skin wrinkling.

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

Lef1 helps stem cells become hair cells by interacting with specific signaling pathways.

MOF controls key genes for skin development by regulating mitochondrial and ciliary functions.

Immune activities and specific genes are important in male pattern baldness.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

Researchers found that certain miRNAs, which affect immune system regulation, are differently expressed in mice with a hair loss condition compared to healthy mice.

Mice without the Sp6 gene have problems developing several body parts, including hair, teeth, limbs, and lungs.

Overexpression of E2F1 can lead to skin tumors and disrupt hair growth.

A new mutation in the HR gene causes hair loss in a specific family.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

Finasteride helps female-pattern hair loss.

Inhibiting AP1 in mice skin causes structural changes and weakens the skin barrier.

ACBP is crucial for healthy skin in mice.