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The conclusion is that androgenetic alopecia and senescent alopecia have unique gene changes, suggesting different causes and potential treatments for these hair loss types.

Researchers used CRISPR/Cas9 to create a goat with a gene that increased cashmere production by 74.5% without affecting quality.

Trichohyalin-like proteins are essential for the development of skin structures like hair, nails, and feathers.

Alopecia areata is a common autoimmune condition causing varying hair loss, diagnosed by specific patterns of inflammation around hair follicles, with several treatment options available.

TGF-alpha is present in sheep and ferret skin and may affect hair growth without directly stimulating cell proliferation.

DNA methylation controls lncRNA2919, which negatively affects hair growth.

Melanin may help melanoma cells grow by aiding their metabolism.

MicroRNAs play a crucial role in skin and hair health, affecting everything from growth to aging, and could potentially be used in treating skin diseases.

Mouse skin can produce and process serotonin, with variations depending on hair cycle, body location, and mouse strain.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

Basonuclin 2 is vital for the development of facial bones, hair follicles, and male germ cells in adult mice, and its absence can lead to dwarfism and abnormal follicles.

Two specific hair keratin genes are active during hair growth and decline as hair transitions to rest.

Keratin gene expression helps understand different types of skin cells and their development, and should be used carefully as biological markers.

Keratin genes change gradually during skin cell development and should be used carefully as biomarkers.

Hair growth is controlled by specific gene clusters and proteins, and cysteine affects hair gene expression in sheep.

Changes in keratin affect skin health and can lead to skin disorders like blistering diseases and psoriasis.

Keratin is crucial for keeping skin cells healthy and its changes can lead to diseases and affect cell behavior.

KAP genes are crucial for hair development and show both shared and unique traits in humans, chimpanzees, and baboons.

Keratins are important for skin cell health and their problems can cause diseases.

New treatments targeting specific genes show promise for treating keratin disorders.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

Keratose, derived from human hair, is a non-toxic biomaterial good for tissue regeneration and integrates well with body tissues.

Human beard hair medulla contains a unique and complex mix of keratins not found in other human tissues.

Understanding hair biology is key to developing better treatments for hair and scalp issues.

Human hair keratins can self-assemble and support cell growth, useful for biomedical applications.

Hair keratins evolved from ancient proteins, diversifying through gene changes, crucial for forming claws and later hair in mammals.

Different combinations of human hair keratins affect how hair fibers form.

Only a few hair-specific keratins are linked to inherited hair disorders.