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Long-term use of dutasteride for enlarged prostate may worsen blood sugar, cholesterol, and erectile dysfunction.

Blocking TSLP reduces skin inflammation and cell overgrowth in psoriasis.

The conclusion is that skin and hair patterns are formed by a mix of cell activities, molecular signals, and environmental factors.

New markers and pathways have been found in skin tumors, helping better understand and diagnose them.

Inflammation affects hair loss; anti-inflammatory treatments may help.

Exosomes from umbilical cord cells fix hearing loss and damaged ear hair cells in mice.

Certain genes are more active in baby scalp cells and can help grow hair when added to adult mouse skin cells.

WNT7A gene expression is higher in early stages of androgenetic alopecia, showing the role of WNT pathway, apoptosis, and inflammation in the disorder.

BMP4-related anomalies can cause a wide range of eye, brain, and hand/foot problems, and new cases show this variability.

Understanding how our bodies interact with mosquito-borne viruses is crucial because there are few treatments and vaccines.

Bald thigh syndrome in sighthounds is caused by structural defects in hair shafts due to downregulated genes and proteins.

DNA can predict physical traits like eye and hair color accurately, especially in Europeans, but predicting other traits and in diverse populations needs more research.

Young HS patients often have other physical and mental health issues, and research on HS covers a wide range of topics including genetics, triggers, treatments, and the need for more data.

Gamma rays did not change hair follicle density but increased white and hypopigmented hairs in mice.

Oriental melon leaf extract may help hair grow and keep it in the growing phase longer.

A girl with Denys-Drash syndrome was misdiagnosed due to biotin affecting her hormone test results.

Newborn screening and gene therapy are expected to improve outcomes for Omenn syndrome patients.

The congress highlighted new gene therapy techniques and cell transplantation methods for treating diseases.

Nuclear shape and chromatin changes affect gene expression in skin cell differentiation.

Kir6.1 mutations in Cantú syndrome increase channel sensitivity and hyperpolarization, while SUR2B mutations do not.

A new MBTPS2 gene variant disrupts fat metabolism and collagen production, causing Osteogenesis imperfecta.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

Heredity and hormones cause common hair loss, and topical minoxidil is the first recommended treatment.

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.

Panax ginseng might help with hair growth and has fewer side effects than synthetic treatments.

Get head MRI for babies with achondroplasia early, use free immunoglobulin light chains to detect certain neurodevelopmental disorders, and video calls work for speech therapy in patients with facial anomalies.

Personalized thiopurine dosing based on NUDT15 genotyping can improve long-term outcomes for ulcerative colitis and Crohn's disease patients.

A 12-year-old girl in Saudi Arabia with Focal dermal hypoplasia showed skin and dental symptoms, highlighting the condition's variability and the need for personalized treatment.

The study aims to create a model to improve personalized and preventive health care.

There is no cure for myotonic dystrophy type 1, so treatment focuses on managing symptoms and complications.