Search

everythinglearnresearchcommunity

for

Search:↓

DNA variants can predict male pattern baldness, with higher risk scores increasing baldness likelihood.

Different types of hair loss in lupus need careful diagnosis for proper treatment.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

Ovarian SAHA syndrome makes women with PCOS more resistant to insulin and increases their risk of blood sugar problems.

Genetic research has advanced our understanding of skin diseases, but complex conditions require an integrative approach for deeper insight.

Blood tests can help understand the genetic differences in people with alopecia areata, including how severe it is and if it's inherited.

The Notch signaling pathway helps in mouse hair development through a noncanonical mechanism that does not rely on RBPj or transcription.

Measuring the distance from the anus to the clitoris may moderately help diagnose polycystic ovary syndrome, especially in certain cases.

Combining skin tissue pathology with genetics has greatly improved the diagnosis and understanding of certain skin diseases.

Adipose-derived stem cells show potential for skin rejuvenation and wound healing but require more research to overcome challenges and ensure safety.

The document concludes that the human keratin gene cluster is complex, with a need for updated naming to reflect over 50 functional genes important for hair and skin biology.

Henna dye improves hair cuticle and thickness but effects vary by hair type and health.

Celsr1 is crucial for skin cell alignment, while Celsr2 has little effect on this process.

The document concludes that diagnosing PCOS requires a thorough approach, considering various symptoms and risks, and calls for improved methods to identify PCOS types and prevent diabetes.

Acne is a common skin condition that can be influenced by diet, lifestyle, and hormones, and requires a treatment approach that includes psychological considerations.

The document explains the difficulty in diagnosing and treating brain diseases caused by the immune system and stresses the need for quick and accurate tests.

Burn scars form abnormally due to changes in wound healing, and more research is needed to improve treatments.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

Too much β-catenin activity can mess up the development of mammary glands and make them more like hair follicles.

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.

A 37-year-old male with severe skin and internal issues has a rare inherited skin condition called dystrophic epidermolysis bullosa.

Thicker melanomas and nodular types are more likely to spread to sentinel lymph nodes.

A man with both Klinefelter syndrome and primary hyperparathyroidism showed a rare combination of symptoms and genetic patterns.

Understanding genetic mutations helps diagnose and treat skin disorders like ichthyosis.

Hidradenitis suppurativa might be a type of autoinflammatory skin disease.

The UD-PrOZA program successfully diagnosed 18% of adult patients with rare diseases, often using genetic testing.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

New digital tools are improving the diagnosis and understanding of irreversible hair loss conditions.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

Targeting Vδ1+T-cells may help treat alopecia areata.