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The peach gene CTG134 helps control the interaction between auxin and ethylene, which could lead to new agricultural chemicals.

CRISPR gene editing reduces harmful molecules in cells from Emery–Dreifuss Muscular Dystrophy patients.

Aire mutation reduces alopecia areata, while Notch4 mutation prevents it in mice.

Antizyme slows skin tumor growth by reducing cell growth in mice.

Lgr5 and the vitamin D receptor are key in controlling skin inflammation and tumor risk in mice.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

Naked-mouse hair lacks certain proteins and has less soluble fibril.

New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.

Overexpression of a specific receptor in mice skin causes skin thinning, early skin barrier formation, eye issues, and hair loss.

A mutation in the KRT82 gene is significantly associated with Alopecia Areata.

NEDD4 and NEDD4L help control intestinal stem cells and prevent tumors by breaking down the LGR5 receptor.

A specific hair protein variant increases the spread of breast cancer and is linked to worse survival rates.

Mutations in the ACTB gene cause Becker’s nevi and may lead to muscle issues in Becker’s nevus syndrome.

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

EGFR deficiency in skin causes hair follicle issues and inflammation.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

LGR5 mainly stays inside cells, moving to the trans-Golgi network, and this process is important for its role in cell signaling.

BRG1 is essential for skin cells to move and heal wounds properly.

A gene variation is linked to hair thickness in Asians.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

Overexpression of R-spondin 3 leads to sparse hair and impaired hair regeneration.

The N gene affects the protein makeup of mouse hair.

PF-05314882 selectively activates androgen receptors without much effect on prostate and may help in prostate cancer treatment and hair loss prevention.

A variant in the KRT31 gene causes a rare hereditary hair disorder called monilethrix.

Pygopus 2 helps ovarian cancer cells grow by aiding ribosomal RNA production, independent of Wnt signaling.

Gsdma3 affects hair growth by controlling Wnt5a, which influences hair cell development.

Peptide nanoparticles can effectively deliver CRISPR-Cas9 to target KRAS mutations in cancer.

Mutations in the DSG4 gene cause fragile, sparse hair in humans, mice, and rats.

BMP receptor IA is essential for proper hair cell differentiation in mice.