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Prolactin affects the production of different keratins in human hair, which could lead to new treatments for skin and hair disorders.

A second domain of high sulfur KAP genes on chromosome 21q23 is crucial for hair structure.

Keratin 79 marks a new group of cells that are key for creating and repairing the hair follicle's structure.

The gene KAP22-1 affects wool yield and fiber shape in sheep.

Coating surfaces with human hair keratin improves the growth and consistency of important stem cells for medical use.

The 3D structure of a key hair protein was modeled, revealing specific helical structures and stabilization features.

A person with a specific gene mutation had extra teeth, unique jaw and hair features not seen before in this condition.

The document concludes that the human keratin gene cluster is complex, with a need for updated naming to reflect over 50 functional genes important for hair and skin biology.

The study concluded that a protein important for hair strength is regulated by certain molecular processes and is affected by growth phases.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

The KRTAP7-1 gene is very similar across different cattle and yak breeds and likely plays a role in hair strength and shape.

A KRT71 mutation in Hereford cattle in Uruguay causes thin, curly hair and scaly skin.

Keratin-associated proteins have ancient origins and were used for different purposes before being adapted for hair in mammals.

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

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.

The Foxn1 gene mutation causes hairlessness and immune system issues, and understanding it could lead to hair growth disorder treatments.

Bleaching hair damages protein structure, especially keratin, leading to weakened hair.

The transition from growth to regression in Cashmere goat hair follicles involves changes in expression of genes related to keratin and cell differentiation.

A genetic mutation in the LIPH gene causes tightly curled hair that stops growing in some Japanese individuals.

FGF-5 promotes Cashmere goat hair growth by increasing keratin genes and reducing certain LncRNA and target genes.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

Genes related to keratin, skin cell differentiation, and immune functions are key in hedgehog skin and spine development.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

Genetic mutations can cause hair growth disorders by affecting key genes and signaling pathways.

Mutations in the PADI3 gene are linked to a higher risk of scarring hair loss in women of African descent.

Mutations in Plcd1 and Plcd3 together cause severe hair loss in mice.

New research has found 14 genes linked to the risk of developing alopecia areata, improving understanding and treatment options.

Genetic testing confirmed a young girl has Atrichia with Papular Lesions due to mutations in the hairless gene.

Inherited ichthyoses cause widespread skin scaling and thickening due to gene mutations.

Keratosis pilaris is a common skin condition where hair follicles get clogged with keratin, mostly on the arms and thighs.