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The LncRNA AC010789.1 slows down hair loss by promoting hair follicle growth and interacting with miR-21 and the Wnt/β-catenin pathway.

Different types of stem cells exist within individual skin layers, and they can adapt to damage, transplantation, or tumor growth. These cells are regulated by their environment and genetic factors. Tumor growth is driven by expanding, genetically altered cells, not long-lived mutant stem cells. There's evidence of cancer stem cells in skin tumors. Other cells, bacteria, and genetic factors help maintain balance and contribute to disease progression. A method for growing mini organs from single cells has been developed.

The study concluded that a protein important for hair strength is regulated by certain molecular processes and is affected by growth phases.

Multi-omics techniques help understand the molecular causes of androgenetic alopecia.

Genetically modified stem cells from human hair follicles can lower blood sugar and increase survival in diabetic mice.

Mutations in the vitamin D receptor cause hereditary vitamin D-resistant rickets, leading to poor bone health and requiring high calcium doses for treatment.

Keratin 79 is linked to liver damage and may help diagnose liver diseases.

Non-liganded Vitamin D Receptor is crucial for healthy skin and hair.

Meis2 is essential for touch sensation and proper nerve connection to touch receptors in certain skin areas of mice.

Non-classical 21 hydroxylase deficiency is an underdiagnosed cause of female hair loss and polycystic ovarian syndrome.

Losing both ERBB2 and ERBB3 receptors in mice causes significant skin problems and inflammation.

A new gene mutation causes insulin resistance in a girl and her mother.

Mice with a changed Hr gene lose and regrow hair due to changes in the gene's activity.

Gene mutations can cause problems in male genital development.

Children's hair grows in different types from before birth through puberty, with growth rates and characteristics varying by age, sex, and race.

Longer CAG repeat lengths in the androgen receptor gene are linked to higher testosterone levels in women with PCOS.

The ITGB6 gene is important for tissue repair and hair growth, and mutations can lead to enamel defects and other health issues.

A gene mutation causes woolly hair in a Syrian patient.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

Certain gene variations are not a major cause of male infertility in Nigerian men.

The HGCA tool helps identify genes that work together by analyzing their co-expression patterns.

UVB radiation changes the levels of certain microRNAs in skin cells, which may affect cell survival and hair growth.

Effective treatments for spinal and bulbar muscular atrophy are not yet available; more research is needed.

Hairless gene not strongly linked to baldness.

Gene therapy shows promise for enhancing physical traits but faces ethical, safety, and regulatory challenges.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

Longer GGN repeats in the androgen receptor gene are linked to polycystic ovary syndrome.

Changes in the HR gene have influenced hair growth and may lead to hair loss conditions in humans.