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The wavy coat in NCT mice is caused by multiple genes, including a mutation in the Prss53 gene.

New LPA receptors (LPA4, LPA5, LPA6) have diverse roles in the body.

Four specific genes are linked to keloid formation and could be potential treatment targets.

New therapies for Birt–Hogg–Dubé syndrome are being developed based on understanding the FLCN gene's role.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

Double-stranded RNA activates a pathway that causes a skin protein to be expressed in the wrong place.

A specific gene variant is linked to a higher risk of hair loss from chemotherapy in breast cancer patients.

Lrig1 and Lgr6 stem cells help maintain hair follicles and influence skin cancer development.

Nε-(carboxymethyl) lysine delays hair growth by blocking a key protein.

A rare genetic mutation caused severe symptoms in a 6-year-old girl with mandibuloacral dysplasia type A.

A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

A clinically suspected melanoma appeared benign under the microscope but was confirmed by specific tests and a rare mutation.

HDAC6 helps keep ovarian follicles dormant, extending female fertility.

Collagen XVII and CD151 affect cell movement, with CD151 inhibiting migration when bound to integrins.

High lactate dehydrogenase activity is not necessary for the growth of squamous cell carcinoma.

Integrin α6 helps identify different neural crest cell types in the skin.

Deleting a specific protein in skin cells disrupts normal hair growth and development.

Researchers found a genetic region that influences the number of coat layers in dogs.

Mutations in the KRT16 gene can cause skin and nail disorders.

ILC1-like cells can cause alopecia areata by disrupting hair follicle immunity, suggesting a new treatment approach.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

A genetic variant in the GJB6 gene likely caused the Labrador's paw pad condition.

A genetic mutation in the LIPH gene causes a rare hair disorder with sparse, curly hair.

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

Lrig1 marks a unique group of stem cells in mouse skin that can become different skin cell types.

New lipid/fiber microplexes improve mRNA therapy for degenerative diseases by enhancing cell function and treatment effectiveness.

T cell subsets are crucial in kidney cancer, and a new model predicts patient outcomes using key genes.

LC-OCT is an effective new method for diagnosing classic lichen planopilaris.

CD98hc's role in skin health decreases with age.