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The gene for Clouston syndrome in a large Indian family is located in the 13q11-q12.1 region.

Not having enough or having too much of the protein Grainyhead-like 3 leads to various developmental problems.

Blocking a certain signal in the gp130 receptor can improve tissue healing and lessen osteoarthritis symptoms.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

Hairless protein can both repress and activate vitamin D receptor functions, affecting gene regulation.

The zinc finger protein 3 in Arabidopsis thaliana reduces plant growth and root hair development.

A girl had rickets due to a gene mutation affecting vitamin D response.

Smad4 is important for healthy hair follicles because it helps produce a protein needed for hair to stick together and grow.

TCF/Lef1 is essential for skin barrier function by regulating lipid metabolism.

Certain genetic variations are linked to hair loss in Mexican men.

High lactate dehydrogenase activity is not necessary for the growth of squamous cell carcinoma.

High amphiregulin in the skin is a bad sign for acute graft-versus-host disease.

Mutations in the androgen receptor gene cause androgen insensitivity, leading to female traits in genetically male individuals.

CRABP2 helps increase the growth of cells important for hair growth by activating a specific growth pathway.

A specific gene mutation causes woolly hair and hair loss.

Androgen receptor activity is influenced by hormones, co-factors, modifications, and mutations.

Hairless gene not strongly linked to baldness.

A gene mutation causes curly hair and hair loss in rats.

Increased 14-3-3 proteins may block hair cycle regression, causing hair loss.

Overexpression of IKZF1 and Ikaros causes hair loss in mice similar to alopecia areata.

Targeting amphiregulin may improve treatment for fibrosis and cancer.

Key genes and RNAs related to hair growth in sheep were identified, aiding future breeding improvements.

Certain HSD3B1 gene types are linked to worse prostate cancer outcomes and affect treatment response and other health conditions.

Mice with LSS deficiency showed hair loss and cataracts, similar to humans, and can help in understanding and treating this condition.

OsPHR2 gene causes excessive phosphate in rice shoots, affecting plant growth and root development.

Higher hair follicle density leads to more wool in rabbits, influenced by specific genes and lncRNAs.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

Targeted therapy with Ustekinumab significantly improved a skin condition called ILVEN, which is caused by mutations in the CARD14 gene.

Higher activity in lichen planopilaris is linked to certain immune and tissue genes.

Light sheet fluorescence microscopy effectively measures calcium changes in Arabidopsis root hairs.