Search

everythinglearnresearchcommunity

for

Search:↓

SR-ECDi helps better understand and map the chiroptical properties of solid chiral materials.

The research found that the properties of solid-state Electronic Circular Dichroism (ss-ECD) are influenced by the orientation of local crystals, which could help in examining and mapping chiral materials like pharmaceutical ingredients.

A specific DNA region controls skin cell gene expression by working with certain proteins.

TCDD disrupts skin stem cells, causing skin issues like chloracne.

Women with nonclassical congenital adrenal hyperplasia may have a higher risk of fertility issues and miscarriages, and should get genetic counseling.

CRISPR/Cas systems show promise for cancer treatment by targeting miRNAs, but delivery and specificity challenges remain.

Different mutations in the 5 alpha-reductase-2 gene were found in affected individuals in the Dominican Republic, suggesting no common ancestry.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

Increased ornithine decarboxylase makes normally tumor-resistant mice more sensitive to tumors.

The type of tumor suppressor gene lost affects the behavior of skin cancer.

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

CYLD mutations cause a variety of skin tumors with symptoms starting around age 16, and treatments are currently limited.

CK 19 expression is higher in more severe skin cancers.

Genetic variants in specific genes cause central centrifugal cicatricial alopecia.

Cedrol may be an effective treatment for colorectal cancer.

The DiLiCre mouse model is an effective tool for precise genome editing using light.

Lysine carboxymethyl cysteinate (LCC) protects skin from UVB damage by activating autophagy.

Changing the direction of cuts can make it easier to put in implants.

Super-enhancers control CD25 expression in specific cell types, affecting immune function.

CCCA is a scarring hair loss condition mainly in African descent women, possibly caused by genetics and hairstyling, treated with gentle hair care and medications.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

CXXC5 is a protein that controls cell growth and healing processes, and changes in its activity can lead to diseases like cancer and hair loss.

Genetic variations contribute to over 10% of recurrent early pregnancy loss cases.

Oxidized trichocyte keratin has a helical dislocation in its structure.