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Injecting monocyto-angiotropin into hare skin increases hair growth by forming new blood vessels.

A specific gene mutation causes complete hair loss without other health issues.

Alopecia Areata is an autoimmune disease affecting hair follicles, influenced by genetic and environmental factors, with rodent models being essential for research.

Altering the keratin 17 gene in mice hair follicles caused temporary hair issues, but changes were minimal and short-lived.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

The protein Gnαs is found more in black mice than white mice and may influence their coat color.

Copper treatments increase copper in all tissues, but brindled female mice accumulate much more copper in their kidneys without clinical effects, unlike brindled male mice where brain copper deficiency is clinically significant.

Hair follicles in the back of the rosette fancy mouse have reversed orientations due to a gene mutation.

A new mouse model for vitiligo helps study immune responses and potential treatments.

Scientists made a mouse that shows how a specific protein in the skin changes and affects hair growth and shape.

A mouse gene mutation increases the risk of skin cancer.

The HCR gene contributes to psoriasis risk.

Heat treatment increases hair loss in certain mice.

Alopecia areata can be triggered by specific immune cells without genetic or environmental factors.

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

The transgene likely activated an oncogene or interrupted a tumor suppressor gene, causing melanoma in mice.

The Msx2 gene affects feather development in Hungarian white geese and a specific gene variation could indicate feather quality.

Scientists restored fertility in male mice lacking a key fertility gene by using a modified gene.

Agouti and AGRP affect pigmentation and obesity, with implications for metabolic disorders.

Removing hair from mice without reproductive glands led to grey hair, possibly helping to understand greying in aging.

The harlequin ichthyosis mouse mutation causes thick skin and early death, resembling a human skin disorder.

A new gene mutation is linked to monilethrix in the studied family.

Homozygous K5Cre transgenic mice have wavy hair and faster cancer progression.

Cupric chloride treatment corrected abnormal Purkinje cell development in brindled mice.

The mutant HR bmh protein mis-localizes in cells, affecting skin and hair development.

Two new gene mutations cause a rare hair disorder.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

Proteomic analysis can identify genetic differences in mouse hair, helping understand hair defects and variations.

Overexpression of hurpin in mice leads to abnormal skin and higher skin cancer risk.