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Notch signalling helps skin cells differentiate and prevents tumors.

MicroRNAs could improve skin tissue engineering by regulating cells and changing the skin's bioactive environment.

Genetic changes in mice help understand skin and hair disorders, aiding treatment development for acne and hair loss.

Overexpression of sPLA2-IIA in mouse skin reduces hair stem cells and increases cell differentiation through JNK/c-Jun pathway activation.

People with Epidermolysis bullosa have many health problems including poor oral health, which is often neglected due to other medical issues.

Cronkhite-Canada syndrome is rare, has a poor prognosis, and requires early diagnosis and ongoing treatment.

Coffee bean residue extract helps hair growth by activating cell processes.

Hair follicle sampling is a practical method for measuring biomarkers in children with and without Fragile X syndrome.

People with hair loss conditions often have more mental health issues like depression and anxiety compared to those without hair loss.

Loose Anagen Syndrome causes easy-to-pull, thin hair, mainly in young girls, and improves with age.

The document says that treating the root cause of hair follicle damage is crucial to prevent permanent hair loss, and treatment options vary.

Hair restoration surgery can effectively increase pubic hair density, with patient satisfaction and natural results largely depending on the chosen hair pattern and graft design.

The conclusion is that a systematic approach is key for treating symmetrical alopecia in dogs, but treatment may not always be necessary.

The EDAR gene mutation leads to thinner and more deformed hair shafts.

A mother and daughter have a rare genetic hair loss disorder with no effective treatment.

WNT10A helps esophageal cancer cells spread and keep renewing themselves.

Loose anagen hair syndrome is caused by structural abnormalities in the hair follicle's inner root sheath.

The study concluded that PKP1 is essential for skin integrity and hair growth, and its dysfunction causes the symptoms of ectodermal dysplasia/skin fragility syndrome.

The document concludes that early diagnosis and treatment are crucial for children with hair loss to prevent permanent damage, although not all conditions can be effectively treated.

The document concludes that careful design of genetic fate mapping experiments is crucial for accurate cell lineage tracing in mice.

Genes related to pigmentation, body rhythms, and behavior change during hares' seasonal coat color transition, with a common genetic mechanism in two hare species.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

Successful eyebrow restoration can be done using careful hair transplant techniques and choosing the right patients.

Fungal infection was the main cause of hair loss in Egyptian children studied.

Scientists have found specific genes linked to different hair loss conditions, which could lead to new treatments.

People with early hair loss may have a higher chance of enlarged prostate and metabolic syndrome, so they should be checked for urinary and metabolic issues.

An 11-year-old Greek girl was diagnosed with a rare genetic disorder, highlighting the importance of genetic testing and family history.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

Some domesticated animals have the same genetic skin diseases as humans, which can help doctors understand human genetic mutations.

Ruxolitinib significantly improves multiple autoimmune conditions in APS-1 patients.