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The study concludes that mutations in the AEBP1 gene can cause a form of Ehlers-Danlos syndrome and should be considered in diagnosis.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

Laser-assisted drug delivery has shown improved treatment outcomes for skin conditions and has potential to reduce side effects and treatment time.

Hair greying is linked to reduced ATM protein in hair cells, which protects against stress and damage.

Researchers found a genetic region that influences the number of coat layers in dogs.

Certain variations of the HDAC9 gene can increase or decrease stroke risk in the Chinese population.

Researchers developed a cost-effective 66 K SNP chip for cashmere goats that is accurate and useful for genetic studies.

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

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

Certain genetic variations in OCT1 may improve insulin sensitivity with metformin in women with PCOS.

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

Certain gene variants in estrogen receptors are linked to polycystic ovary syndrome, mainly affecting metabolism, in Tunisian women.

Genetic variants at 20p11 increase baldness risk in Chinese Han people.

MC4R gene variants not linked to female hair loss.

Selective breeding caused the unique curly hair in Mangalitza pigs.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

Porphyra-334 may help reduce wrinkles and promote hair growth.

BMP4-related anomalies can cause a wide range of eye, brain, and hand/foot problems, and new cases show this variability.

Key genes can rewire networks, changing skin appendage types.

SA linked to mitochondrial issues and oxidative stress, while AGA involves disrupted hair growth genes.

CD201+ fascia progenitors are essential for wound healing and could be targeted for treating skin conditions.

Researchers identified genes in scalp hair follicles that may affect hair traits and hair loss.

Genetic differences within ethnic groups may affect prostate cancer treatment effectiveness.

Environmental cues can change the fate and function of epithelial cells, with potential for cell therapy.

ESR2 gene linked to female-pattern hair loss.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

Hair follicles in the back of the rosette fancy mouse have reversed orientations due to a gene mutation.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

Certain genetic variants linked to immune response increase the risk of alopecia areata in Taiwanese people.

Low-coverage sequencing is a cost-effective way to identify genes related to wool traits in rabbits.