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The congress highlighted new gene therapy techniques and cell transplantation methods for treating diseases.

The PTGER2 gene is highly active in Cashmere goat skin and its activity changes with the hair growth cycle.

The conference presented findings on how vitamin D levels, genetic factors, and lifestyle choices like smoking and yoga affect various health conditions and diseases.

5α reductase type 2 enzyme mutation and oxidative stress may increase androgenetic alopecia risk in Egyptians.

IVIG therapy significantly improved symptoms in a patient with APS-2 and SPS.

The meeting focused on understanding, diagnosing, and finding treatments for irreversible hair loss diseases.

New patents show progress in developing drugs targeting the Wnt pathway for diseases like cancer and hair loss.

OCIAD2 and DCN genes affect hair growth in goats by having opposite effects on a growth signaling pathway and inhibiting each other.

Mast cells play a significant role in hair loss conditions like male pattern hair loss and alopecia areata.

The conclusion is that certain genetic factors and blood types may affect COVID-19 severity, but changes in ACE2 and TMPRSS2 genes are not clearly linked to it.

Cancer rates are increasing in developed countries, with estrogen, aging, low vitamin D3, and HPV infection as common causes.

A rare genetic mutation causes resistance to vitamin D, leading to severe rickets and requiring high doses of calcium and vitamin D for treatment.

The absence of functional sebaceous glands causes hair follicle destruction and scarring alopecia.

Leptin-deficient mice, used as a model for Type 2 Diabetes, have delayed wound healing due to impaired contraction and other dysfunctional cellular responses.

Different versions of the KRTAP6-2 gene in goats can lead to thinner cashmere fibers.

Minoxidil 2% is more effective for female hair loss, but botanicals have fewer side effects.

A rare genetic disease causes rickets and often hair loss in young children, which can improve with specific treatments.

The research found that male pattern hair loss is mostly genetic and involves hair thinning due to hormonal effects and changes in gene expression.

Higher levels of miR-203 may contribute to hair loss in alopecia areata.

Blocking COX, especially COX-2, in the skin can reduce inflammation and pain and may help prevent skin cancer.

Alopecia areata is a common autoimmune disease affecting about 2% of people, causing significant disability and often associated with mental health issues and other autoimmune conditions.

The LRRK2-G2019S mutation in Parkinson's disease has a lifetime penetrance of 25-35%, and finasteride may help reduce symptoms in adult male Tourette syndrome patients.

The scraggly mutation causes hair loss and skin defects in mice.

A 2-year-old boy had no hair and unusual organ placement, and it's unclear if it's genetic or coincidental.

2011 dermatological research found new skin aging markers, hair loss causes, skin defense mechanisms, and potential for new treatments.

Blocking miR-27a increases sheep hair follicle stem cell growth and decreases cell death, which could help improve wool quality and treat hair loss.

In 2011, there were major scientific breakthroughs in cancer treatment, immunity, Parkinson's, virus simulation, schizophrenia, hair growth, lung cancer, and medical grafts.

Ritlecitinib and brepocitinib effectively regrow hair in alopecia areata patients.

Mice studies show that Protein Phosphatase 2A is crucial for cell growth, development, and disease prevention.

New method finds genetic links between Type 2 Diabetes and Prostate Cancer not seen before.