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Researchers created a fully functional, bioengineered skin system with hair from stem cells that successfully integrated when transplanted into mice.

Monilethrix is a rare genetic hair disorder that's hard to treat.

Skin's epithelial stem cells are crucial for repair and maintenance, and understanding them could improve treatments for skin problems.

Genes and hormones cause hair loss, with four genes contributing equally.

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

Recent findings suggest that genetic factors, immune system issues, and skin cell defects might contribute to the development of hidradenitis suppurativa.

Tandem repeats significantly influence hair color, especially darker shades, across different ancestries.

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

A 10-month-old boy with a rare combination of genetic conditions has severe immune deficiency and treatment challenges.

The study found that in Latin America, ancestry varies by location, influences physical traits, and affects how people perceive their own heritage.

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

Trichoscopy can diagnose monilethrix, a genetic hair defect causing hair thinning and loss.

Certain immune-related proteins are higher in people with alopecia and their healthy relatives, hinting at a genetic link.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Certain genes influence immunoglobulin levels in Chinese Holstein cows, which can improve calf health.

Metabolic syndrome's individual issues are real and need treatment to reduce diabetes and heart disease risks.

The document concludes that while there are promising methods to control CRISPR/Cas9 gene editing, more research is needed to overcome challenges related to safety and effectiveness for clinical use.

Alopecia Areata is an autoimmune hair loss condition that needs more research for better treatments.

Scientists found genes linked to the growth of high-quality brush hair in Chinese Haimen goats.

Sardinians were historically short due to a mix of genetics and factors like disease and poor nutrition, but recent height increases suggest better living conditions had a bigger impact.

Researchers identified genes and proteins that may influence wool thickness in sheep.

Three dogs with a rare skin condition improved with treatment.

PCOS in lean women is a serious health condition with implications beyond fertility, affecting metabolism and increasing cardiovascular disease risk.

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

Selective breeding can enhance immunity in dairy cattle.

Acne is caused by genetics, diet, hormones, and bacteria, with treatments not yet curative.

The document concludes that alopecia areata is an autoimmune disease without a definitive cure, but treatments like corticosteroids are commonly used.

Using CRISPR for gene editing in the body is promising but needs better delivery methods to be more efficient and specific.

Glutathione helps Arabidopsis roots adapt to low phosphate by regulating a specific growth pathway.

The document concludes that ongoing research using animal models is crucial for better understanding and treating Alopecia Areata.