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New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

Mutations in the glucocorticoid receptor gene cause reduced sensitivity to glucocorticoids and may lead to poor response to treatment.

Indian head cactus extract may help hair grow by boosting important cell activity and gene expression.

Japanese researchers created new hair follicles from human cells that grew hair when put into mice, and other findings showed a link between eye disease severity and corneal thickness, gene mutations affecting hearing and touch, and the safety of the shingles vaccine for adults over 50.

Intravenous calcium therapy is a safe and effective treatment for a rare type of rickets.

STK11 gene variations do not predict how well metformin will work for PCOS, but may affect hair loss and excess hair growth.

A 532 nm laser at 15 J/cm2 speeds up tendon healing by increasing tendon stem cell growth and tendon-related gene activity.

An 86-year-old man with prostate cancer was diagnosed with a rare, low-grade breast cancer and underwent surgery but declined additional hormone therapy.

A boy's growth and immune problems were caused by a new mutation in the STAT5B gene.

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

Melatonin may help with nerve pain, a hepatitis C drug is effective but has side effects, a treatment for mouth sores works but can cause blood issues, ear reconstruction with an implant is safe, HIV transmission from mother to child in Taiwan is now 0% with treatment, certain blood problems are more common in people with a tongue condition, a gene and being overweight are linked to hair loss in some women, a new technique could reduce radiation for lung nodule patients, a hepatitis treatment may lower cancer recurrence after a procedure, and adding extra screening improves tuberculosis detection in patients with lung infections.

Organoids help study and treat genetic diseases, offering personalized medicine and therapy testing.

Different cell types work together to repair skin, and targeting them may improve healing and reduce scarring.

Hair loss has many causes and treatments, but future research aims for better solutions.

Two rare genetic diseases cause severe rickets in children due to defects in vitamin D metabolism.

Obesity worsens PCOS symptoms, and PCOS may lead to more weight gain; managing both requires a holistic approach that includes mental health.

Foxp3 is crucial for regulatory T cell function, and targeting these cells may help treat immune disorders.

Men are more likely to have severe respiratory viral infections like COVID-19 due to hormonal and genetic differences, while women generally have stronger immune responses.

A patient with Wilson's disease showed hair-pulling behavior as an initial symptom.

Woodhouse-Sakati syndrome can cause writer's cramp and other varied symptoms, highlighting the importance of genetic testing for diagnosis.

Stem cells from whiskers can be transplanted to stimulate hair growth.

Researchers discovered potential origins and new treatments for skin cancer, including biomarkers for melanoma and therapies that reduce tumor growth.

Dr. Rodney Sinclair uses a detailed grading system to diagnose female pattern hair loss, recommends daily spironolactone and minoxidil for treatment, and believes genetics play a role in the condition.

Researchers developed a method to grow hair follicles using special beads that could help with hair loss treatment.

Some treatments for hereditary hair loss are effective but vary in results and side effects; new therapies show promise but need more research.

Wnt-3a helps grow more skin stem cells, which could lead to new hair loss treatments.

The document covers various dermatological treatments and conditions.

Removing a methyl group from the ITGAV gene speeds up bone formation in a specific type of bone disease model.

A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

Damaging mutations in NFKB2 cause a severe and distinct form of primary immunodeficiency with early-onset and often ACTH-deficiency.