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Researchers created a mouse model for Cushing's syndrome to study glucocorticoid excess and potential treatments.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

Oral contraceptives lower testosterone levels in women, especially those with certain genetic traits, and may be linked to increased breast cancer risk.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

Alopecia Areata is an autoimmune disease affecting hair follicles, influenced by genetic and environmental factors, with rodent models being essential for research.

Sex neurosteroids cause different effects on hippocampal synaptic plasticity in males and females.

New acne treatments show promise as alternatives to traditional therapies.

Sebaceous glands play a key role in skin health, immunity, and various skin diseases.

Looking at skin can help find and treat serious diseases early.

Normal levels of DHT can reduce belly fat and increase muscle, but too much can lead to hair loss, prostate issues, and possibly heart disease.

Researchers identified specific genes that are important for mouse skin cell development and healing.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

The study concluded that testing hormone levels after stimulation is not reliable for identifying carriers of 21-hydroxylase deficiency; genetic testing is necessary.

Finasteride significantly reduced tics and obsessive-compulsive symptoms in patients with Tourette syndrome.

Flightless I protein affects hair growth, with low levels delaying it and high levels increasing hair length in rodents.

Certain genetic markers linked to reproductive potential were identified by their impact on a protein's ability to bind to genes.

No strong genetic link to other skin conditions was found, but some genetic factors may make people more likely to get seborrheic dermatitis.

Embryonic and adult stem cells are valuable for improving skin grafts and cell therapy.

Certain variations of the HDAC9 gene can increase or decrease stroke risk in the Chinese population.

Removing myelin protein zero-like 3 in mice leads to better metabolism and resistance to obesity.

Blocking 5α-reductase can harm memory and brain structure, and increase harmful brain changes in male mice used for Alzheimer's disease research.

Hair and skin can regenerate without bulge stem cells due to other compensating cells.

Combining skin tissue pathology with genetics has greatly improved the diagnosis and understanding of certain skin diseases.

Female mice with disrupted 5α-reductase 1 had significant metabolic issues, including stress response problems, insulin resistance, liver fat buildup, and obesity.

Hair loss gene linked to prostate issues.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

Certain liver diseases respond well to specific treatments and have varying risks for liver cancer.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.