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A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

Human hair follicles can assess carcinogen metabolism and imidazole compounds might be effective anticarcinogens.

11α-Hydroxyprogesterone is changed into different substances by certain enzymes and may play a role in prostate cancer.

Overexpressing Tβ4 in cashmere goats improves hair fiber traits and increases cashmere yield.

Individuals with this condition often develop male traits and identities at puberty despite being raised as females.

Cylindromas likely originate from hair follicle stem cells, not sweat glands.

Differences in cashmere quality between goat breeds are linked to specific genes affecting hair follicle development.

Circular RNA ERCC6 helps activate stem cells important for cashmere goat hair growth by interacting with specific molecules in an m6A modification-dependent way.

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

Foxn1 gene regulation is crucial for thymus development but not for hair growth.

Dihydrotestosterone increases the activity of an enzyme in pubic skin cells that converts testosterone to dihydrotestosterone.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

Prostasin has two roles in skin: one for normal skin development without needing activation, and another for proper hair growth that requires activation.

A specific type II hair keratin was identified and found in hair cortex and tongue cells.

The N gene affects the protein makeup of mouse hair.

A new gene mutation causes vitamin D resistance and rickets, treatable with calcium therapy.

Severe genetic variants in children with a specific adrenal condition match predicted symptoms well, but milder variants do not.

MCPIP1 in myeloid cells is important for skin cancer development and healthy hair growth.

The peach gene pCTG134 helps control the interaction between auxin and ethylene hormones during fruit ripening.

A 22-year-old woman with a rare genetic condition was successfully treated to develop normal female characteristics and regular menstruation.

Keratinocytes can reduce the survival of certain melanoma cells, suggesting new therapy paths.

A new mouse mutation causes skin and hair issues, influenced by another gene.

A mutation in the KRT25 gene causes woolly hair and hair loss.

Certain gene mutations are linked to wool quality in sheep and could help in breeding for better wool.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

YAP and TAZ proteins are necessary for the development of two types of skin cancer.

Truncated hHb1 keratin may play a role in breast cancer cell transformation.

Some women with excess hair growth have a hormone condition that can't be diagnosed by blood or urine tests alone.