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ME1 and PPAR signaling may influence hair loss in androgenetic alopecia.

A new method was created to measure metformin in hair, showing potential for monitoring treatment and medical investigations.

New method makes important drug ingredients more easily without needing extra purification steps.

A mutation in the HOXC13 gene causes hair and nail problems in a Syrian family.

The hair lotion with methyl myristate in niosomes treats grey hair faster and better than the free form.

Brain-made chemicals can control nerve cell function differently in various parts of a mouse's brain, which may help us understand neurological conditions.

A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.

Deleting the BRD4 protein in certain skin cells causes hair loss and skin inflammation.

The environment around the time of conception can change the VTRNA2-1 gene in a way that lasts for years and may affect disease risk.

PBX1 reduces aging and cell death in stem cells by boosting SIRT1 and lowering PARP1.

Stress can cause hair to turn gray by depleting stem cells.

RNA editing significantly affects hair growth and follicle cycling in the Tianzhu white yak.

Ginsenoside Re from Panax ginseng may prevent hair loss by maintaining autophagy and Wnt signaling in hair cells.

A new hair dye method uses polyphenols and oxidation to create a long-lasting brown color on gray hair.

Methionine intake changes tooth germ development in newborn rats.

Mice genetically modified to produce more Del1 protein had faster hair regrowth.

The study created a mouse model to mimic degenerative diseases for testing tissue repair and new therapies.

A patient with a rare disease had a unique genetic mutation linked to their symptoms.

Enzymes that change arginine to citrulline are important for skin barrier and hair formation, and their malfunction can lead to skin conditions and hair disorders.

Finasteride reduces certain behaviors caused by D1-like receptor agonists but not by D2-like receptor agonists in mice.

Stopping alcohol after long-term use causes anxiety and changes brain chemicals.

Altering SSAT affects fat metabolism and body fat in mice.

Duodenal mucosal resurfacing did not improve insulin sensitivity or reproductive function in women with PCOS.

The Msx2 gene affects feather development in Hungarian white geese and a specific gene variation could indicate feather quality.

The NUDT15 R139C variant causes thiopurine-induced leukocytopenia through a different mechanism than previously thought in Japanese patients with inflammatory bowel disease.

Acitretin improved monilethrix symptoms temporarily, but they returned after stopping treatment.

Overexpression of the glucocorticoid receptor in mice causes developmental defects similar to ectodermal dysplasia.

Blocking DGAT1 reduces oil gland size in mice and dogs, but only mice experience hair loss.

Scientists made a mouse model of a serious skin cancer by changing skin cells with a virus and a specific gene, which is similar to the disease in humans.

The document provides a method to prepare human scalp tissue for studying hair follicles at the single-cell level.