Search

everythinglearnresearchcommunity

for

Search:↓

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

The new microwell device helps grow more hair stem cells that can regenerate hair.

Certain KIR genes in Indian SLE patients are linked to disease severity and could be biomarkers.

Understanding gene expression in hair follicles can reveal insights into hair growth and disorders.

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.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

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

Certain genetic variations in the FST gene are linked to better wool quality in Chinese Merino sheep.

Blocking the FGF5 gene in sheep leads to more fine wool and active hair follicles due to changes in certain cell signaling pathways.

Hair restoration surgery techniques have evolved, with focus on patient selection and realistic goals, and future advancements may include cloning and gene therapy.

Cat color patterns are determined early in development by gene expression and epidermal changes, with the Dickkopf 4 gene playing a crucial role.

Advanced therapies like gene, cell, and tissue engineering show promise for hair regrowth in alopecia, but their safety and effectiveness need more verification.

DHT affects bone growth by altering gene activity in osteoblasts, potentially complicating steroid use.

The research found that the gene activity in mouse skin stem cells changes significantly as they age.

KDML105 bran extract may help with hair growth and prevent hair loss.

The congress highlighted new gene therapy techniques and cell transplantation methods for treating diseases.

Differences in gene expression and methylation patterns found in AGA patients suggest potential targets for future treatments.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

Targeted therapy with Ustekinumab significantly improved a skin condition called ILVEN, which is caused by mutations in the CARD14 gene.

The conclusion is that the nuclear lamina and LINC complex in skin cells respond to mechanical signals, affecting gene expression and cell differentiation, which is important for skin health and can impact skin diseases.

Deleting the CRIF1 gene in mice disrupts skin and hair formation, certain proteins affect hair growth, a new compound may improve skin and hair health, blood cell-derived stem cells can create skin-like structures, and hair follicle stem cells come from embryonic cells needing specific signals for development.

A deficiency in the TTC7A gene causes immune problems, gut issues, and hair loss.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

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

The Hairless gene is crucial for hair cell development, affecting whether skin cells become hair or skin and oil gland cells.

Keratin protein production in cells is controlled by a complex system that changes with cell type, health, and conditions like injury or cancer.

DNA methylation likely doesn't cause different lambskin patterns in Hu sheep.

Keratin gene expression helps understand different types of skin cells and their development, and should be used carefully as biological markers.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.