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A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

The genes KRT25 and SP6 affect curly hair in horses, with KRT25 also causing hair loss. If both genes are mutated, the horse gets curly hair and hair loss. KRT25 can hide the effect of SP6.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

Genomic profiling for myeloid cancers can find important inherited mutations, but it's challenging when these mutations aren't related to the patient's symptoms.

Sons of mothers with polycystic ovary syndrome (PCOS) have a higher risk of obesity and insulin resistance, possibly due to certain genes and factors passed down from their mothers.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

FGF5 gene mutations cause unusually long eyelashes by affecting hair growth regulation.

Autofluorescence can sort plant cells without labeling.

The symposium concluded that understanding the molecular mechanisms of skin aging could lead to better clinical practices and treatments.

Our microbiome may affect the development of the hair loss condition Alopecia Areata, but more research is needed to understand this relationship.

Cutaneous Lymphadenoma is a unique skin tumor with specific protein markers and common gene mutations that may cause continuous cell growth.

The study found two new mutations in a Chinese patient with severe biotinidase deficiency.

Autism's genetics are linked with early age of puberty and less hair loss, but not with hormone levels or polycystic ovary syndrome.

The UK's EDS National Diagnostic Service found that early diagnosis, lifestyle advice, and regular check-ups are crucial for managing vascular Ehlers-Danlos syndrome. A combination of losartan and bisoprolol can reduce vascular events, improving survival and quality of life.

The combination treatment showed a higher response rate but no significant survival benefits.

Both shampoos increased scalp germ numbers but did not change the overall microbial community composition.

Mutations in mitochondrial DNA might significantly contribute to the development of Polycystic Ovarian Syndrome.

The specific skin disease variant p.(Arg2000Trp) in plectin can cause a wide range of symptoms, which should be considered when diagnosing patients.

The follicular unit extraction method for hair transplants is a technique with benefits and drawbacks.

Cantú syndrome is caused by mutations in the ABCC9 gene.

Vimentin is involved in regulating the hair growth cycle in Inner Mongolian Cashmere goats.

The conclusion is that certain dog and cat breeds are prone to Malassezia dermatitis, which can be diagnosed with skin tests and treated with antifungal shampoos or medications, and preventing relapses involves managing underlying issues and maintaining good hygiene.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

New treatments like nanotechnology show promise in improving skin cancer therapy.

PPARγ is essential for maintaining healthy skin, controlling inflammation, and ensuring proper skin barrier function.

Certain miRNAs play a key role in the growth of cashmere by affecting hair follicle development and regeneration.

Understanding how acne develops in different diseases could lead to new treatments.

The conference concluded with plans for joint research into children's skin conditions and emphasized the importance of collaboration and patient-focused research.

PCOS is a complex condition in women that can lead to health issues, and lifestyle changes are the best management approach.

Alopecia areata patients have more Propionibacterium acnes and less Staphylococcus epidermidis on their scalps.