Search

everythinglearnresearchcommunity

for

Search:↓

Removing a methyl group from the ITGAV gene speeds up bone formation in a specific type of bone disease model.

Nociplastic type pain, common in Chronic Overlapping Pain Conditions, is a complex, heritable trait linked to 24 unique genetic factors and 127 genes, with potential shared mechanisms in cognitive, personality, and metabolic traits.

ATP-dependent chromatin-remodeling complexes are crucial for gene regulation, cell differentiation, and organ development in mammals.

Skin and hair can regenerate after injury due to changes in gene activity, with potential links to how cancer spreads. Future research should focus on how new hair follicles form and the processes that trigger their creation.

Cat color patterns are determined early in development by gene expression and epidermal changes, with the Dickkopf 4 gene playing a crucial role.

Scientists restored fertility in male mice lacking a key fertility gene by using a modified gene.

The KRTAP11-1 gene promoter is crucial for specific expression in sheep wool cortex.

Hoxc13 gene expression and skin thickness change similarly during cashmere goat hair follicle development.

A circular RNA helps cashmere goat hair cells become hair follicles by blocking a molecule to boost a gene important for hair growth.

Common gene patterns may cause skin autoimmune diseases.

Injecting CHIR-99021 into goose embryos improves feather growth by changing gene activity and energy processes.

Mongolian gerbils heal wounds differently than mice, with unique protein levels and gene expression that affect skin repair.

Chicken feather gene mutation helps understand human hair disorders.

Newborn screening and gene therapy are expected to improve outcomes for Omenn syndrome patients.

Abnormal gene expression related to keratin causes hair loss in certain mice.

Hairless mammals evolved quickly in both gene and non-gene areas related to skin and hair.

The research found that male pattern hair loss is mostly genetic and involves hair thinning due to hormonal effects and changes in gene expression.

The document concludes that understanding hair biology is key to treating hair disorders, with gene therapy showing potential as a future treatment.

Exosomes from skin cells can boost hair growth by stimulating a gene called LEF1.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

Cantú syndrome is caused by mutations in the ABCC9 gene.

Chromosomal changes, including those in the WRN gene and rDNA, may significantly contribute to aging.

Disrupting the Flcn gene in mice causes early kidney cysts and tumors, which can be treated with rapamycin.

Mutations in the androgen receptor gene cause Androgen Insensitivity Syndrome, affecting sexual development.

The fuzzy gene is crucial for controlling hair growth cycles.

The gene Msx2 is crucial for hair follicle regeneration during wound healing.

Hair keratins evolved from ancient proteins, diversifying through gene changes, crucial for forming claws and later hair in mammals.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

Progeria, a disease that causes early aging, is linked to a gene mutation and helps us understand normal aging.