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Removing anthrax toxin receptor 1 in pigs prevents Senecavirus A infection and causes a rare disease similar to GAPO syndrome.

A new gene causes hairlessness and skin cysts in rats.

Lack of KSR1 stops certain skin tumors in mice.

The naked mutation in mice causes hair loss and helps identify keratin genes.

Silencing certain circadian clock genes increases skin pigmentation.

Sphingosine 1-phosphate affects inflammation and gene expression in different aorta cells.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

Id proteins, especially Id2 and Id3, are crucial for hair follicle development and stem cell regulation.

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

PBX1 helps hair stem cells grow and change by turning on certain cell signals and preventing cell death, which may be useful for hair regrowth treatments.

Sweating can potentially be controlled through olfactory receptors, with β-ionone playing a key role, and responses may vary between genders.

Hair follicle cells help protect against immune attacks by regulating T-cell activity.

DKK-1 gene linked to hair loss in AGA and AA patients; more research needed for potential therapy.

Dysplastic nevi have unique gene expressions, making them distinct from common melanocytic nevi.

The prolactin gene polymorphism doesn't affect cashmere quality in these goats.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

Deleting Snai2 and Snai3 causes fatal autoimmunity.

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

The Apc gene is crucial for normal skin and thymus development.

Lef1 is essential for normal skin, hair growth, and healing wounds in mice.

miR-133a-3p and miR-145-5p help goat hair follicle stem cells differentiate by controlling NANOG and SOX9.

TSC22D genes are key in metabolic diseases and cancer, offering potential as treatment targets.

YAP1 helps fat cell formation by influencing the Hippo pathway.

Matriptase-2 helps control iron levels by suppressing hepcidin, and its deficiency can cause iron-deficiency anemia.

WNT10A mutations cause varied symptoms in patients with odonto-onycho-dermal dysplasia.

Dab2 protein is crucial for hair follicle stem cell renewal and preventing early aging.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

Zebrafish help understand genetic causes of skin pigment disorders like albinism.

Mutations in TBX3 cause horses to have more even hair color instead of Dun camouflage.

PCR genotyping in cre-loxP mice can be inaccurate due to unintended gene deletions in non-target tissues.