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Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

The conclusion is that genetic testing is important for diagnosing and treating various genetic hair disorders.

Different types of cells in the eye express specific keratins at various stages of development.

A protein in plants needs to bind two lipids to help with root hair growth, and this process is similar across different plant species.

Rapp-Hodgkin syndrome, AEC, and EEC are different expressions of the same genetic disorder caused by TP63 gene mutations.

IL-1 family cytokines are crucial for skin defense and healing, but their imbalance can cause skin diseases.

TGM3 is important for skin and hair structure and may help diagnose cancer.

New treatments for ichthyosis, like protein replacement and gene therapy, show promise and may become standard care.

Thiopurines help treat IBD but require genetic testing to avoid side effects.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

The protein p53 directly reduces the production of Keratin 17, a skin and hair protein, in rats with radiation dermatitis.

A new model can predict drug-disease links well, helping drug research.

A genetic mutation caused severe rickets and alopecia in an Indian patient, but high-dose calcium and phosphate treatment improved their condition.

Researchers found genes and microRNAs that control curly fleece in Chinese Tan sheep.

Hairless protein affects hair follicle structure by regulating the Dlx3 gene.

Different species use the same genes for tooth regeneration.

Mice with extra human KLK14 had hair and skin problems, including weaker cell bonds and inflammation, linked to Netherton syndrome.

Genetic defects in the glucocorticoid receptor gene can cause conditions with abnormal sensitivity to stress hormones, and other factors may also affect this sensitivity.

Mutations in the NR3C1 gene cause a rare condition that affects hormone signaling and can lead to various symptoms, with dexamethasone as a treatment option.

Key genes crucial for sheep hair follicle development were identified, aiding fine wool breeding and human hair loss research.

Keratin 26 affects cashmere goat hair growth and is influenced by various treatments.

Hairless protein reduces Msx2 gene activity, affecting hair follicle development.

The research confirms that Hidradenitis Suppurativa is characterized by increased inflammation, disrupted skin cell organization, and abnormal metabolic processes.

Mutations in the DSG4 gene cause fragile, sparse hair in humans, mice, and rats.

A gene mutation causes early keratinocyte maturation leading to hair loss in Olmsted syndrome.

Researchers found genes and genetic variants linked to sheep wool and skin wrinkles.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

Sheep and goat hair fibers are complex due to keratin-associated proteins, which are important for fiber properties and growth.

When skin blisters, healing the wound is more important than growing hair, and certain stem cells mainly fix the blisters without helping hair growth.

Corin helps control salt and sweat release in sweat glands.