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The N363S gene variant does not cause higher adrenal androgen levels in women with polycystic ovary syndrome.

Researchers found a new mutation causing total hair loss from birth.

A Japanese patient with IFAP syndrome had a severe MBTPS2 gene mutation but showed milder symptoms than previously observed cases.

The document concludes that hair analysis is not good for assessing nutrition but can detect long-term heavy metal exposure.

CD201+ fascia progenitors are essential for wound healing and could be targeted for treating skin conditions.

A woman with a rare hormone resistance condition also had missing teeth and hair loss, which might be new symptoms of her genetic disorder.

Lipase H is important for hair follicle function and shaping hair fibers.

Recent selection on immune response genes was identified across seven ethnicities.

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

New technologies show promise in healing wounds, treating cancer, autoimmune diseases, and genetic disorders.

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.

Half of people with Alopecia Areata may see hair regrowth within a year without treatment, but recovery is unpredictable.

Planarian regeneration begins with a specific gene activation caused by injury, essential for healing and tissue regrowth.

Despite progress, better treatments and understanding are needed for the high rates of long-term issues and deaths linked to eating disorders.

PCOS affects women's health by increasing the risk of diabetes, heart disease, and reproductive issues.

Noggin overexpression delays eyelid opening by affecting cell death and skin cell development.

Using CRISPR for gene editing in the body is promising but needs better delivery methods to be more efficient and specific.

Polycystic Ovary Syndrome is linked to higher risk of hypertension and heart disease.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

The document concludes that anti-dsDNA antibodies are not unique to SLE and their use as indicators is doubtful, highlighting the need for better understanding and classification of the disease.

The document concludes that early diagnosis and treatment are crucial for children with hair loss to prevent permanent damage, although not all conditions can be effectively treated.

Hair disorders are caused by a complex mix of biology, genetics, hormones, and environmental factors, affecting hair growth and leading to conditions like alopecia.

The study found no common cause for a girl's crystalline cataract and uncombable hair, suggesting their co-occurrence might be coincidental.

Thyroid diseases may contribute to autoimmune skin diseases, and more research is needed on their relationship.

AR gene not major factor in female hair loss; different from male hair loss.

No link found between new male baldness genes and female hair loss.

Hormones and genetics play key roles in male and female baldness, which can affect mental health and may be linked to other health issues.

A gene mutation in mice causes permanent hair loss and skin issues.

The 25Up study collected extensive data on mental disorders and related factors in Australian twins and siblings to investigate the genetics of psychiatric illnesses.