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Heavily hunted wolves have higher stress and reproductive hormone levels.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

The review suggests that other immune cells besides CD8+ T cells may contribute to alopecia areata and that targeting regulatory cell defects could improve treatment.

Teriflunomide effectively reduces relapse rates and disease progression in multiple sclerosis but is not safe for use during pregnancy.

Zebrafish need MYC and FGF to regenerate inner ear hair cells.

Isotretinoin can cause serious birth defects and needs careful use, especially in pregnant women.

The article discusses debates on hair transplant techniques, safe donor areas, PRP use, and practitioner qualifications in hair restoration.

A Korean boy's skin and digestive symptoms were caused by a rare genetic disorder that affects zinc absorption, and he got better with zinc supplements.

A3B5 can reduce skin pigmentation and slow melanoma growth.

The same genetic mutation in Sjögren-Larsson syndrome can lead to different levels of severity, suggesting other factors influence the symptoms.

Child abuse is linked to higher BMI, but not because of hair cortisol or cortisone levels.

Combined prednisone and cyclosporine therapy led to excellent hair regrowth and improved well-being.

Laser ablation ICP-MS is effective for tracking trace elements in polar bear hair over time.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

The revised Chinese Symptom Checklist-90 is more reliable and valid for psychological assessments.

New genetic mutations linked to rare skin disorders were found in three newborns.

Hair protein composition is similar across different races and shapes.

Girls had higher stress hormone levels during school due to social and emotional issues, while boys had higher overall hormone levels with slight changes when school started.

Natural products and phytochemicals may help with hair regrowth, but more research is needed.

Some women with PCOS have rare genetic variants linked to the condition.

Early recognition and treatment of tinea capitis are crucial to prevent severe scalp issues and prolonged therapy.

Scabies is the most common skin condition among children in Pakistan, with poor hygiene and contact with animals being major risk factors.

A heterozygous mutation in HTRA1 can cause severe CARASIL symptoms.

A new goat gene affects cashmere fiber thickness; certain variations can make the fibers coarser.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

A new hydrogel with micronized amnion helps achieve better, scar-free skin healing.

Facial plastic surgeries and aesthetic procedures are becoming more popular in India, with a preference for non-surgical options and effective treatments for facial enhancement and hair loss.

The conclusion is that certain physical signs in the body can indicate past acute and chronic stress, which may help in child abuse investigations.

Rogaine can stop hair loss in women, and other treatments like certain pills, light therapy, and special shampoos may also work.

Alopecia areata is an autoimmune disease with genetic links, treatable with certain medications, and can affect mental health.