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Stem cell therapies show promise for treating various diseases but face challenges in clinical use and require better monitoring techniques.

Cells from certain embryo parts can induce head formation in another embryo, involving complex signaling pathways.

Mutation in hairless gene may increase hair loss risk.

The document concludes that regenerating functional ectodermal organs like teeth and hair is promising for future therapies.

Loose Anagen Hair Syndrome is found in black-haired Indian children and is often missed, especially in boys.

More men are getting non-surgical cosmetic treatments due to increased income and social acceptance, with less invasive options being preferred.

Chinese medicine may help hair growth and reduce hair loss in androgenetic alopecia.

PGA-4HGF may help treat hair loss by activating hair growth pathways and extending the hair growth phase.

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

The report suggests that hair loss in Cronkhite-Canada syndrome may be caused by alopecia areata incognita, as shown by a patient's improvement with treatment.

Men with certain types of baldness at age 45 may have a higher risk of colon cancer and colorectal adenoma.

Applying minoxidil can help improve hair growth in people with hair loss caused by LIPH gene mutations.

Over half of the children had abnormal hair under a microscope, with many having genetic hair conditions.

No genetic link between prostaglandins and hair loss found.

CD61 is important for mouse tooth cell growth and works through Lgr5.

Keratin is crucial for keeping skin cells healthy and its changes can lead to diseases and affect cell behavior.

Tranilast successfully treated a man's skin sarcoidosis when other treatments failed.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

Recent hair loss research shows some progress, especially in understanding male pattern baldness, but effective treatments for many types of hair loss are still lacking.

The review shows how to properly diagnose and treat the loss of eyebrow and eyelash hair.

Acitretin helped improve hand mobility and skin condition in a patient.

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

The Foxn1(-/-) nude mouse shows disrupted and expanded skin stem cell areas due to high Lhx2 levels.

A man with KID syndrome developed a rare cancer in a long-term skin infection.

A woman's hair changed to a dry, tangled texture that's hard to comb after treatment with spironolactone, suggesting the medication might cause such hair changes.

The document concludes that hair analysis is not good for assessing nutrition but can detect long-term heavy metal exposure.

Deleting the p63 gene in certain cells causes problems in thymus development and severe hair loss in mice.

Deleting the Trf1 protein in mice is safe and may help prevent cancer without major side effects.

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

A 3-year-old girl developed scurvy symptoms that improved with vitamin C but relapsed when supplementation stopped.