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Researchers found that most genes affecting drug responses are not fully covered by commercial SNP chips, suggesting the need for more comprehensive tools to optimize drug selection based on genetics.

Researchers found two new genetic variants linked to Alzheimer's disease.

The Androgen Receptor could be a target for treating diseases like cancer, but more research is needed to confirm the effectiveness of potential treatments.

A defective protein in progeria causes cell death and atherosclerosis, but a treatment targeting cell stress may reduce these effects.

The symposium concluded that understanding how different species repair tissue and how this changes with age can help advance regenerative medicine.

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

Found different proteins in balding and non-balding cells, giving insight into hair loss causes.

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.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

Skin abnormalities can indicate immunodeficiency due to shared origins with the immune system.

Certain genetic variants in the androgen receptor are linked to higher PSA levels, potentially affecting prostate cancer screening outcomes.

Blocking interferon-gamma might help treat various autoimmune diseases.

Exosomes from umbilical cord cells fix hearing loss and damaged ear hair cells in mice.

Researchers created immortal human skin cells with constant testosterone receptor activity to study hair loss and test treatments.

Astrotactin proteins are important for brain and skin development and are linked to several neurodevelopmental disorders.

People with Myotonic Dystrophy type 1 are more likely to have certain skin conditions, but not more likely to get skin cancer.

Mutations in Plcd1 and Plcd3 together cause severe hair loss in mice.

A new mutation in the AGPAT2 gene causes severe fat tissue loss and related health issues by reducing the protein's levels.

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

Runx genes are important for stem cell regulation and their roles in aging and disease need more research.

A new gene mutation may allow some piebaldism patients to regain skin color in white patches.

Researchers found a gene in hamsters that responds to male hormones and may be indirectly controlled by them.

The new ELISA method is reliable and eco-friendly for checking the quality of Pueraria candollei.

Rapamycin may help treat Leigh syndrome by targeting protein kinase C.

Bald thigh syndrome in sighthounds is caused by structural defects in hair shafts due to downregulated genes and proteins.

Harlequin mutant mice have hair loss due to low AIF protein levels and retroviral element activity.

A protein called ectodysplasin-A2 increases a hair growth inhibitor in balding cells, which could be a target for hair loss treatment.

The most different genetic segment between Africans and East Asians is the EDA2R/AR region, with two main types influenced by population changes and natural selection, and linked to baldness.

Lymphatic vessels are essential for health and can be targeted to treat various diseases.

Melatonin affects cashmere growth in goats by influencing stem cell and certain signaling pathways.