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Acne in dark skin is influenced by environmental factors and can lead to hyperpigmentation, with various treatment options available.

Genetic defects in testosterone production can cause hormonal and developmental disorders, and more research is needed to understand androgen regulation and develop safer treatments.

Dermatologists diagnose and manage melanoma more effectively than general practitioners.

Activating TRPV4 in skin cells helps regrow hair in mice, possibly offering a treatment for hair loss.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

The HIF-2α/ARNT complex is important for hair follicle development by controlling cell growth.

Finasteride doesn't affect omeprazole metabolism in Japanese people.

Topical PUVA and tacrolimus ointment can effectively and safely treat infant alopecia universalis.

PNKP is essential for keeping adult mouse progenitor cells healthy and growing normally.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

Photodynamic therapy may not work for erythroplasia of Queyrat and could lead to invasive squamous cell carcinoma.

A man with testotoxicosis was fertile despite low FSH levels, suggesting high testosterone may allow sperm production without FSH.

The cornified envelope is crucial for skin's barrier function and involves key proteins and genetic factors.

Hair follicles in the back of the rosette fancy mouse have reversed orientations due to a gene mutation.

The girl's condition improved with treatment, showing no new autoimmune diseases and hair regrowth.

The Asiatic lion has very low genetic diversity and unique genetic traits, highlighting the need for its conservation.

Genetics, stress, and health issues can cause early hair greying, which affects self-esteem, and there's no cure, only hair dye.

Identifying nonclassic congenital adrenal hyperplasia and carriers of CYP21 mutations is challenging, and genetic counseling is recommended due to their prevalence.

The document explains the genetic causes and characteristics of inherited hair disorders.

Hdac1 and Hdac2 help maintain and protect the cells that control hair growth.

Certain cells in the adult mouse ear come from cranial neural crest cells, but muscle and hair cells do not.

Low-dose radiation therapy may improve brain function in some Alzheimer's patients and is generally well-tolerated.

Tiny particles from 3D-grown skin cells speed up wound healing by promoting blood vessel growth.

Early detection and multidisciplinary treatment are crucial for managing Papillon-Lefévre syndrome.

Possible link between hair loss and metabolic syndrome, with RANTES as a potential clue.

Removing centrosomes from skin cells leads to thinner skin and stops hair growth, but does not greatly affect skin cell differentiation.

OM-X® helped prevent negative effects of Vitamin C deficiency in mice, suggesting it could protect organs and regulate metabolism.

Benzothiazepines like diltiazem reduce anxiety in mice by making neurosteroids.

The research showed that CRISPR/Cas9 can fix mutations causing a skin disease in stem cells, which then improved skin grafts in mice, but more work on safety and efficiency is needed.