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A protein called GIS3 is important for the growth of root hairs in Arabidopsis by controlling two genes with the help of certain growth signals.

A new CDH3 gene mutation was found in a Spanish patient with sparse hair and eye issues.

Applying L-methionine and L-serine to the skin promotes the most hair growth.

The enzymes Tet1, Tet2, and Tet3 are important for the development of hair follicles and determining hair shape by controlling hair keratin genes.

Two new gene mutations cause a rare hair disorder.

DNA methylation is essential for skin and hair follicle development, and could be a target for treating skin diseases.

Methionine intake changes tooth germ development in newborn rats.

Hydrogen sulfide disrupts protein function and root hair growth in plants by modifying proteins.

The hairless (hr) gene is essential for normal hair follicle function and its mutation leads to hair loss.

Targeting the MC-5-HT-HTR2A axis may help treat chronic itching.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

Hirsute women have lower type 2 17β-HSD enzyme levels, which improve with treatment.

Researchers successfully made new compounds for hormone level tests, but one attempt led to an unexpected product, correcting a past error.

Inhibiting class I HDACs helps maintain hair growth ability in skin cells.

The enzymes Tet2 and Tet3 are important for skin cell development and hair growth.

Idiopathic hirsutism may be linked to increased enzyme activity.

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

Higher homocysteine levels may inhibit hair growth and are linked to androgenetic alopecia.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

Mutations in the HOXC13 gene cause hair and nail development issues.

Removing a methyl group from the ITGAV gene speeds up bone formation in a specific type of bone disease model.

A specific gene mutation causes sparse, brittle hair in a family.

Hidradenitis suppurativa may be more severe in people with Mediterranean fever gene mutations.

A gene mutation in mice causes skin defects and early death.

m⁶A methylation is crucial for proper wound healing and tissue repair.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

The L457(3.43)R mutation in the human lutropin receptor causes increased activity and hormone insensitivity, leading to precocious puberty.

Tet2 and Tet3 enzymes are essential for controlling hair growth by affecting DNA demethylation and gene expression in mice.

Overexpression of SSAT causes hair loss and skin issues, but reducing putrescine can help.

The protein EZH2 blocks microRNA-22, increasing STK40 protein, which helps hair follicle stem cells change and grow hair.