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A new genetic tool improves the study of hair growth and potential hair disorder treatments.

Hair root analysis can effectively detect somatic mosaicism in double cortex syndrome.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

A mutation in the iRhom2 gene causes hairless mice due to abnormal hair follicle development.

CRISPR/Cas9 and prime editing can potentially fix skin disorder genes safely and effectively.

Frizzled 3 and Frizzled 6 together control the orientation of mouse hair follicles.

Homozygous K5Cre transgenic mice have wavy hair and faster cancer progression.

A specific gene mutation causes a severe skin disorder in a family.

A unique gene mutation was found in a family with monilethrix.

Sphynx cats are hairless and Devon Rex cats have curly hair due to specific genetic mutations.

Blocking the JAK/STAT pathway may help reduce skin sensitivity in Xeroderma pigmentosum.

Researchers created a mouse model for Cushing's syndrome to study glucocorticoid excess and potential treatments.

Mutations in the Whn gene affect hair keratin gene expression differently.

Melanoma risk tools need improvement, certain gene mutations cause skin diseases and could be treated by targeting those mutations, skin wrinkling may relate to lung aging due to genetic factors, and oxidative stress affects hair loss but can be reduced in low oxygen.

The gene NM_026333 slows down aging by affecting the NCX1 pathway and could be targeted for anti-aging treatments.

Scientists created a cell model to study and find treatments for a skin disease called RDEB.

Researchers created a new mouse model for studying scleroderma.

A mutation in the Adam10 gene causes freckle-like spots on Hairless mice.

A new gene mutation is linked to monilethrix in the studied family.

A gene mutation in mice causes permanent hair loss and skin issues.

Overexpressing the MSX-2 gene in mice causes skin and hair growth issues.

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

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

The Glu413Lys mutation in keratin affects hair stability, while Glu413Asp does not.

Identical twins with a rare KRT 86 gene mutation both have the hair disorder monilethrix.

A mutation in the KRT86 gene causes hair fragility in a Turkish family.

Melanoma risk tools need improvement, a gene mutation causes a hair disorder that might be treated by managing cell stress, a potential therapy for a skin-ear disorder involves blocking cell channels, skin wrinkling may indicate lung aging regardless of smoking, and oxidative stress might contribute to common baldness.

Some cells may slow melanoma growth, a protein could affect skin pigmentation, a gene-silencing method might treat hair defects, skin bacteria changes likely result from eczema, and a defensin protein could help treat multiple sclerosis.

MOF controls skin development by regulating genes for mitochondria and cilia.