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The conclusion is that genetic differences affect how the cochlea heals after hair cell loss, which may challenge the creation of hearing loss treatments.

New method finds genetic links between Type 2 Diabetes and Prostate Cancer not seen before.

Scientists created hair-growing skin models from stem cells, which could help treat hair loss and skin diseases.

The study created hair-bearing skin models that lack a key protein for skin layer attachment, limiting their use for certain skin disease research.

Scientists made a mouse model of a serious skin cancer by changing skin cells with a virus and a specific gene, which is similar to the disease in humans.

Overactive Wnt signaling in mouse skin stem cells causes acne-like cysts and shrinking oil glands, which some treatments can partially fix.

Hidradenitis Suppurativa has genetic links, with certain gene mutations more common in patients and a third of cases having a family history.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

Fibrodysplasia ossificans progressiva is a rare genetic disorder that causes extra bone growth and symptoms of premature aging.

Thiopurines help treat IBD but require genetic testing to avoid side effects.

Overexpression of sPLA2-IIA in mouse skin reduces hair stem cells and increases cell differentiation through JNK/c-Jun pathway activation.

Alopecia areata involves complex immune and genetic factors, with potential treatment targets identified, but more research is needed.

Personalized treatments for hair loss are becoming more effective by using genetic information.

New treatments are needed for PCOS that target its genetic, hormonal, and metabolic causes.

Low-dose radiation affects hair stem cell function and survival by changing their genetic material's structure.

Baricitinib and its combination with lonafarnib improve fat cell formation in certain genetic disorders.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

Lhx2 is a crucial regulator of the Sonic Hedgehog signaling in early mouse retinal development.

Some lesser-known causes of PCOS include autoimmune issues, genetic mutations, and changes in the body's microbiome.

The study found that alopecia areata is strongly linked to autoimmune diseases and may indicate a genetic predisposition to such conditions.

Hair follicle studies suggest that maintaining telomere length could help treat hair loss and graying, but it's uncertain if mouse results apply to humans.

Knocking out certain genes in mice helps understand skin and hair growth problems.

FGF5 gene mutations cause long hair in domestic cats.

The transgene likely activated an oncogene or interrupted a tumor suppressor gene, causing melanoma in mice.

The complement system might be involved in the development of alopecia areata and could lead to new treatments.

New tools show that in fish, NPY increases feeding and somatostatin decreases it.

Certain immune molecules and stress affect hair loss, and while genes play a role, more research is needed to fully understand and treat it.

Hair graying may be caused by stem cell depletion from stress or melanocyte damage.

Biotin and biotinidase are essential to prevent health issues, and deficiencies require lifelong supplementation.