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Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

Different skin stem cells help heal wounds, with hair follicle cells becoming more important over time.

Hair diversity is influenced by complex genetics and environmental factors, requiring more research for practical solutions.

The LRRK2-G2019S mutation in Parkinson's disease has a lifetime penetrance of 25-35%, and finasteride may help reduce symptoms in adult male Tourette syndrome patients.

Finasteride reduces Tourette syndrome symptoms, but results may be limited due to potential biases.

Mutations in the PTPRQ gene cause significant balance issues in mice due to hair bundle defects in the inner ear.

Accurate diagnosis is key for treating different kinds of hair loss, and immune response variations may affect the condition and treatment results.

Genetic variations affecting skin structure play a key role in severe acne.

Female pattern hair loss has unclear causes, possibly involving genetics, hormones, and environment, and needs better treatments.

CLE40 and CRN/CLV2 pathways have opposite effects on root growth in Arabidopsis.

Hoxc genes control hair growth through Wnt signaling.

Heparan sulfate is important for hair growth, preventing new hair formation in mature skin, and controlling oil gland development.

Non-classic congenital adrenal hyperplasia is a common disorder causing symptoms like acne and infertility, and it's managed based on symptoms, not just test results. Treatment can improve fertility and reduce miscarriage risk.

MicroRNAs play a crucial role in skin and hair health, affecting everything from growth to aging, and could potentially be used in treating skin diseases.

CRAC channels are crucial for the development and function of specialized immune cells, preventing severe inflammation and autoimmune diseases.

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.

Finger length ratios are not linked to the number of specific gene repeats affecting testosterone sensitivity.

Asian hair is generally straight and thick, with unique disorders and properties, and more research is needed to understand it fully.

No consistent link between genotype and phenotype in 5-α-Reductase type 2 deficiency.

Low serum complement levels in SLE patients don't always match with disease flares; monitoring C3 and C4 is useful, but cell-bound complement products might better indicate disease activity.

Some people experience severe, long-lasting side effects from fluoroquinolone antibiotics, leading to the recommendation of limited use and increased awareness of these risks.

Certain genetic variations in the SHBG gene are linked to an increased or decreased risk of PCOS in Mediterranean women.

Genetics play a role in acne, but how exactly they contribute is not fully understood.

Finasteride may help reduce symptoms in male Tourette syndrome patients.

Most patients with Porphyria Cutanea Tarda had skin blisters and were often affected by hepatitis C and alcohol abuse, with differences between familial and sporadic cases.

PDGF signaling is crucial for maintaining and renewing hair follicle stem cells, which could help treat hair loss.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

High lactate dehydrogenase activity is not necessary for the growth of squamous cell carcinoma.

The review found no clear link between vitamin D receptor gene variations and polycystic ovary syndrome.

Certain DNA variants can predict straight hair in Europeans but are not highly specific.