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People with PCNT mutations often develop severe insulin resistance and early-onset diabetes during childhood or adolescence.

New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.

Changes in KRT17 gene activity linked to wool production in Angora rabbits.

Keratins help protect cells, aid in cancer diagnosis, and influence cancer behavior and treatment.

Formyl-peptide receptor agonists could be new anti-inflammatory drugs.

Vitamin D is crucial for skin health and managing skin diseases.

Testosterone is linked to cardiovascular risk factors and stroke, but its exact role is unclear.

The Rotterdam Study aims to understand various diseases in older adults.

Androgenic alopecia in men is mainly linked to family history, hormonal imbalances, and metabolic issues, but can also be influenced by lifestyle habits, environmental factors, and deficiencies in certain vitamins and microelements like copper.

Afro-textured hair needs personalized care due to its unique genetic traits.

A new gene, JMJD1C, may affect testosterone levels in men.

Scientists found 53 keratin genes in yaks that are important for hair growth and share similarities with those in other animals.

Polycystic Ovary Syndrome (PCOS) is a common condition in women that can cause metabolic, reproductive, and psychological issues, and requires lifestyle changes and medication for management.

People with alopecia areata have more Th17 cells and fewer Treg cells, which may be key to the condition's development.

Type 1 diabetes often occurs with other autoimmune diseases, and personalized treatment based on genetics can improve outcomes.

The document concludes that the development of certain tumors is influenced by genetic background and that a specific gene modification can lead to tumor regression and reduced growth.

BMP4 gene is crucial for hair follicle development in Liaoning cashmere goats.

Male and female hair loss have different genetic causes.

Mutations in Plcd1 and Plcd3 together cause severe hair loss in mice.

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

The conclusion suggests a new way to classify bradykinin-mediated angio-oedema based on different causes and its possible link with urticaria, which could improve diagnosis and treatment.

Use antimalarials like hydroxychloroquine for cutaneous lupus, avoid herbal supplements, and focus on lifestyle changes like sun protection.

Hair follicles repair 3D injuries using a 2D healing process.

The document concludes that future heart disease research should account for sex-specific differences to improve diagnosis, treatment, and outcomes.

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 document concludes that PCOS has a strong genetic component, but more research is needed to fully understand the specific genes involved.

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

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

Drug repositioning is becoming more targeted and efficient with new technologies, offering personalized treatment options and growing interest in the field.

The document concludes that more research is needed to fully understand the causes of PCOS.