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M30 is a promising treatment for preventing hair loss during chemotherapy.

Patient-derived melanocytes can potentially treat vitiligo by restoring skin pigmentation.

Keratins are crucial for cell structure, growth, and disease risk.

HLA-DRB5 and other genes may be linked to alopecia universalis.

The document concludes that there are still unknowns about the effectiveness, risks, and detection of performance-enhancing drugs, and doping remains a challenge.

Phosphorylation controls TFEB's location in the cell, affecting cell metabolism and stress response.

Ozone and procaine boost the release of healing factors in platelet-rich plasma.

Genetic defects in the glucocorticoid receptor gene can cause conditions with abnormal sensitivity to stress hormones, and other factors may also affect this sensitivity.

A defective protein in progeria causes cell death and atherosclerosis, but a treatment targeting cell stress may reduce these effects.

New androgen receptor modulators show promise for treating diseases like prostate cancer and muscle wasting.

Bmpr2 and Acvr2a receptors are crucial for hair retention and color.

Poplar seed hairs grow from the placenta at the ovary base, with endoreduplication playing a key role in their development, and share similar cellulose synthesis processes with cotton fibers.

Cattle skin has leptin which might control skin and hair growth.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

FP-1 is a key protein in rat hair growth, active only during the growth phase.

Hair, teeth, and mammary glands develop similarly at first but use different genes later.

Bimatoprost is effective for growing longer, thicker, and darker eyelashes.

MOF controls key genes for skin development by regulating mitochondrial and ciliary functions.

Enzymes play crucial roles in metabolism, health, and disease management.

Human skin can be reconnected to nerves using stem cells, which may help with skin health and healing.

Drosha and Dicer are essential for hair follicle health and preventing DNA damage in skin cells.

The peach gene CTG134 helps control the interaction between auxin and ethylene, which could lead to new agricultural chemicals.

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

The new anti-acne treatment HA-P5 effectively reduces acne by targeting two key receptors and avoids an enzyme that can hinder treatment.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

Beta-HPV and MCPyV are linked to certain skin cancers, with ongoing research and vaccine development.

Congenital Adrenal Hyperplasia is a rare inherited disease causing hormone imbalances, affecting growth, fertility, and heart health, diagnosed through blood tests and treated with medication and lifestyle changes.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

People with Myotonic Dystrophy type 1 are more likely to have certain skin conditions, but not more likely to get skin cancer.

The document concludes that Syndromes of Severe Insulin Resistance are rare disorders with limited treatment options.