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Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

The enzymes Tet1, Tet2, and Tet3 are important for the development of hair follicles and determining hair shape by controlling hair keratin genes.

Disrupting the Tsc2 gene in certain cells leads to thicker skin, larger hair, and changes in hair growth signaling, which can be partly reversed with specific treatment.

UV radiation may cause DNA changes in skin, certain UVB therapy helps psoriasis, a new gene mutation is linked to mild piebaldism, different immune cells affect psoriasis, a drug promotes hair growth, and some cancer drugs could treat skin barrier issues.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

Pangolins have lost some skin-related genes, but kept others, leading to their unique scales and skin features.

Testosterone affects stress hormone levels differently in adolescent and adult male rats.

Birth control pills change the activity of certain inflammation and blood clotting genes in women with PCOS.

Tet2 and Tet3 enzymes are essential for controlling hair growth by affecting DNA demethylation and gene expression in mice.

Enhancers and super-enhancers are key in controlling specific gene activity and can play a role in cancer development.

The nucleus is key in controlling skin growth and repair by coordinating signals, gene regulators, and epigenetic changes.

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.

Future hair loss treatments should aim to extend hair growth, reactivate resting follicles, reverse shrinkage, and possibly create new follicles, with gene therapy showing promise.

Both gene and non-gene areas of DNA evolved to make some mammals hairless.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

Heat stress changes goats' skin and hair at the microscopic level and affects their genes and skin bacteria.

Skin changes in Pseudoxanthoma elasticum patients can indicate the severity of related health issues.

A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.

Understanding and manipulating epigenetic changes can potentially lead to human organ regeneration therapies, but more research is needed to improve these methods and minimize risks.

Goat skin changes with the seasons due to genes affected by daylight and hormones.

Aging changes female scalp cells, likely affecting hair health.

Cetaceans lost hair due to changes in the Hr and FGF5 genes.

Benign Prostatic Hyperplasia may be caused by changes in how the body processes male hormones.

Doxazosin mesylate and saw palmetto cause genetic changes in fruit flies.

Goat skin adapts to seasonal changes through genes that respond to daylight length, affecting hormone levels and potentially making skin cells light-sensitive.

Skin organoids with NCSTN mutation show changes in hair follicle development and higher inflammation, key features of Hidradenitis Suppurativa.

Hair loss in androgenic alopecia patients is linked to changes in certain genes that control cell growth and death.

Hair loss in male pattern baldness is linked to changes in specific genes and proteins that affect hair growth and scalp health.

Buschke-Ollendorff syndrome is a rare genetic disorder causing skin and bone changes, with some cases also showing ADHD or developmental delays.