Search

everythinglearnresearchcommunity

for

Search:↓

The mutant HR bmh protein affects hair follicle formation by failing to repress vitamin D receptor activity.

High LGR5 levels in glioblastoma indicate poor prognosis and are essential for cancer stem cell survival.

A Turkish woman has a hair condition caused by a LIPH gene mutation.

A rabbit gene important for hair development was identified and detailed.

DPR can cause skin, hair, and nail issues, sometimes appearing later in life.

Patients with the same genetic mutation for vitamin D-resistant rickets showed different symptoms but all improved with treatment except for hair loss.

Lichen planopilaris may have a genetic link.

Aconiti Lateralis Preparata Radix helps mouse stem cells grow and turn into bone cells faster than usual methods.

Long noncoding RNAs may help understand rabbit hair follicle density.

Activating TRPMLs helps human cells important for hair growth and increases hair growth in mice.

High levels of auxin increase root hair growth by activating RSL2 and producing ROS, while high phosphate levels hinder growth by repressing RSL2.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

LncRNAs may help improve brain cancer treatment and diagnosis.

Sirolimus and propranolol may reduce abnormal cell growth and improve lymphatic malformations in children.

LEF1 interacts with Vitamin D Receptor, affecting hair follicle regeneration and this could be linked to hair loss conditions.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

AtZP1 protein stops root hair growth in plants by blocking certain genes.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

Rac1 is essential for proper hair structure and color.

Deucravacitinib improves symptoms and reduces inflammation in Lichen Planopilaris.

AHR ligands could treat inflammatory skin diseases.

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

The frizzy mouse and hairless rat mutations are due to changes in the Prss8 gene.

RANK-RANKL signaling is essential for hair growth and skin health.

PAD type III enzyme is specific to rat skin and hair follicles.

Defective nuclear transport may cause gene expression changes in Progeria.

PLDζ2 and NPC4 have different roles in lipid changes and root hair growth in Arabidopsis under low phosphate, with PLDζ2 reducing root hair growth and NPC4 promoting it.