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The Asiatic lion has very low genetic diversity and unique genetic traits, highlighting the need for its conservation.

The cornified envelope is crucial for skin's barrier function and involves key proteins and genetic factors.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

Researchers found 63 genes linked to male-pattern baldness, which could help in understanding its biology and developing new treatments.

With careful management, people with congenital adrenal hyperplasia can have successful pregnancies and become parents.

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.

Bone marrow-derived stem cells improved healing and reduced scarring in second-degree burns in rats.

The report concludes that PCOS is mainly a condition of excess male hormones and its definition may change as new information is discovered.

Anorexia Nervosa and Bulimia Nervosa are complex eating disorders with increasing incidence among young females, significant morbidity, and varying mortality rates, requiring more research for better treatment.

The document concludes that effectively managing PCOS requires a multifaceted approach.

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

New therapies for Birt–Hogg–Dubé syndrome are being developed based on understanding the FLCN gene's role.

Alopecia areata is caused by the immune system attacking hair follicles.

Protein tyrosine kinases are key in male pattern baldness, affecting skin structure, hair growth, and immune responses.

Certain genes and X chromosome patterns may significantly contribute to the development of hair loss.

People with Birt-Hogg-Dubé syndrome often have lung problems and delayed diagnosis, and better recognition of CT scan signs could improve diagnosis and management.

Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.

Mutations in the AR gene cause hair thinning and loss.

Women with PCOS often have skin problems like excessive hair, acne, hair loss, and dark patches, which can be treated with hormonal and non-hormonal therapies.

Oxidative stress is a key factor in the development of Polycystic Ovary Syndrome, and weight management can improve symptoms.

The document concludes that Nonclassic Congenital Adrenal Hyperplasia requires personalized treatment plans to manage symptoms and fertility, with glucocorticoids being a common therapy.

The Rotterdam Study investigates diseases in older adults and has produced many research findings.

Inherited ichthyoses cause widespread skin scaling and thickening due to gene mutations.

The document concludes that proper diagnosis and a multidisciplinary approach are crucial for managing Congenital Adrenal Hyperplasia effectively.

The IRS-2 Asp/Asp genotype may increase the risk of PCOS in Chinese women, especially if they are not obese.

Blocking a specific enzyme can reduce the negative impact of stress hormones on hair growth cells.

The Siah1 and Siah2 genes are active in mouse skin development and hair growth, especially right after birth.

Certain miRNAs might be involved in a hair loss condition called frontal fibrosing alopecia and could possibly help in its diagnosis.

The study found that sweat glands normally suppress immune responses, but this is disrupted in certain skin diseases, possibly contributing to their development.

Researchers created human cells that can turn into sebocytes, which may help study and treat skin conditions like acne.