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The transcription factor Meis2 is essential for touch sensation and proper nerve development in touch receptors.

Alopecia areata causes sudden hair loss, has genetic links, and can be managed but not cured.

Genetic testing is crucial for diagnosing congenital atrichia, a rare condition causing irreversible hair loss.

The letter suggests that the study's comparison group might have affected the results and calls for larger, more detailed future research.

New gene discoveries have improved diagnosis and treatment for skin and hair disorders, but more research is needed to fully understand them.

Genetic testing confirmed a rare skin disorder in a young girl, which improved with zinc supplementation.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

Lhx2 is a crucial regulator of the Sonic Hedgehog signaling in early mouse retinal development.

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.

CCC1 is essential for pH balance and normal cell function in plants.

Skin stem cells in hair follicles are important for touch sensation.

Deleting the MAD2L1 gene is tolerated in certain mouse cancer models.

Mice treatments didn't grow hair, a patient treatment may affect immune response, and people with hair loss often feel anxious or depressed.

CRISPR/Cas9 gene-editing shows promise for improving sheep and goat breeding but faces challenges with efficiency and accuracy.

Genetic risk for PCOS can affect children's growth, metabolism, and development from early life into adulthood.

Certain genetic variations in the AR and ERβ genes can affect androgen levels in women.

Melanoma's complexity requires personalized treatments due to key genetic mutations and tumor-initiating cells.

Treat genetic hair loss early with FDA-approved medications and consider hair transplantation.

Certain genetic markers linked to reproductive potential were identified by their impact on a protein's ability to bind to genes.

Cyclophosphamide often causes gastrointestinal issues, hair loss, and low blood cell counts in Chinese patients with autoimmune diseases.

Certain proteins involved in DNA modification may affect the genetic changes in systemic lupus erythematosus and could indicate the disease's activity.

Two siblings with a genetic mutation had a form of rickets that doesn't respond to vitamin D.

Certain genetic variations in the A2M gene are linked to better milk quality in Murrah buffaloes.

A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.

Certain genetic variations are linked to higher liver enzyme levels in patients treated for chronic hepatitis C with specific drugs.

Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

Younger patients and those with more hair loss are less likely to benefit from oral steroid treatment for hair loss, and low vitamin D may predict relapse.

STK11 gene polymorphism does not predict metformin response in PCOS.

Boron deficiency in maize affects leaf boron levels and nutrient uptake differently depending on root hair presence and soil type.

Both Th1 and Th2 immune responses are increased in alopecia areata, with Th2 response more strongly linked to how severe the disease is.