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The conclusion suggests a new way to classify bradykinin-mediated angio-oedema based on different causes and its possible link with urticaria, which could improve diagnosis and treatment.

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

Neurotrophin-4 increases calcium current in specific mouse neurons through the PI3K pathway.

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

Certain gene variants in estrogen receptors are linked to polycystic ovary syndrome, mainly affecting metabolism, in Tunisian women.

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

Longer GGN repeats in the androgen receptor gene are linked to polycystic ovary syndrome.

KAP9.2 and Hoxc13 genes are important for cashmere growth and vary in activity during different stages.

MC4R gene variants not linked to female hair loss.

A new gene mutation causes hereditary coproporphyria with reduced enzyme activity.

Selective breeding caused the unique curly hair in Mangalitza pigs.

Adult stem cells with Tp63 can form hair and skin cells when placed in new skin, showing they have hidden abilities for skin repair.

Some children in Malaysia with symptoms have either profound or partial biotinidase deficiency, and early testing and treatment are important.

B6.Cg-Tyr c−2J Hr hr /J mice have a stronger delayed sunburn reaction and are good for UV research.

A specific thyroid hormone resistance mutation may be linked to different types of hair loss.

GDNF helps grow hair and heal skin wounds by acting on hair stem cells.

HSD3B1 gene variant and being overweight linked to hair loss in women with polycystic ovary syndrome.

Frontal Fibrosing Alopecia is a poorly understood condition that is hard to treat and causes distressing hair loss.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

Androgens contribute to common male hair loss; more research needed for hair growth medication.

Ro stress hindered ginseng root growth and ginsenoside production, but increased certain hormones and affected gene regulation related to plant growth and stress responses.

Thymic stromal lymphopoietin (TSLP) promotes hair growth, especially after skin injury.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

Ingenol mebutate gel changes gene expression related to skin development and immune response in actinic keratosis.

The KRTAP21-2 gene affects wool length and quality in sheep.

People often underestimate hair loss severity, with fewer seeking treatment, and it's more distressing for women.

Early balding in men might be a male hormonal equivalent of polycystic ovaries syndrome in women.

Genes affecting wool fiber thickness in Angora rabbits were identified, which could help breed finer wool.