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A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

Personalized thiopurine dosing based on NUDT15 genotyping can improve long-term outcomes for ulcerative colitis and Crohn's disease patients.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

The Wnt signaling pathway is not a major factor in the development of keratoacanthoma, a type of skin tumor.

A specific RNA molecule, circCOL1A1, affects the growth and quality of goat hair by interacting with miR-149-5p and influencing cell growth pathways.

Estrogen increases blood vessel growth factor production, while testosterone blocks this increase.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

Researchers found a new mutation causing total hair loss from birth.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

AIRE-deficient rats developed severe autoimmune disease similar to APECED, useful for testing treatments.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

ΔNp63α stops TAp73β from working in skin cancer by blocking its access to specific genes, not by directly interacting with it.

Cells treated with Wnt-10b can grow hair after being transplanted into mice.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

Two microRNAs affect hair follicle development in sheep by targeting specific genes.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

Ichthyosis with confetti is a genetic skin disorder with consistent ectodermal malformations and various KRT10 gene mutations.

Epidermolytic ichthyosis can be inherited in a semidominant way with mild symptoms in carriers.

Mutations in three genes cause Uncombable Hair Syndrome, leading to frizzy hair that can't be combed flat.

A new mutation in the Connexin 26 gene was found in a patient with KID syndrome, expanding the known disorders linked to this gene.

The vitamin D receptor can work without its usual activating molecule.

Certain genetic markers linked to wool quality in Rambouillet sheep were identified, which can guide better breeding choices.

New technologies show promise in healing wounds, treating cancer, autoimmune diseases, and genetic disorders.

The CAP1 gene helps control ammonium levels and is necessary for the proper growth of root hairs in Arabidopsis.

Vitamin D boosts a specific gene activity in kidney cells that could improve heart and kidney function.

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

GLI2 increases follistatin production in human skin cells.

Hair's resistance to wear varies by ethnicity and treatment, with less wear indicating stronger hair.