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LPA3 signaling in the uterus is crucial for placental formation and fetal development.

Researchers found a genetic region that influences the number of coat layers in dogs.

A mutation in the Soat1 gene causes hair structure defects and other health issues in AKR/J mice.

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

Mutations in the DSG4 gene cause specific hair and scalp issues.

PDF2 senses specific lipids and regulates root growth and gene expression in Arabidopsis.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

A gene mutation causes a rare hereditary hair loss, offering potential for new treatments.

Several genes, including Hox-7A, Stra6, and Lim-1, are involved in normal palate formation.

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

Sry may regulate fatty acid metabolism and shows different expression levels in rat tissues.

MCHR2 gene duplications may be linked to alopecia areata.

Over-expression of Sp2 can lead to cancer by preventing proper stem cell differentiation.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

Harlequin mutant mice have hair loss due to low AIF protein levels and retroviral element activity.

LRIG1 protein affects hair growth by regulating skin receptors, leading to hair loss when overexpressed.

Blocking LFA-1 prevents hair loss in mice.

The hr gene is linked to hair loss in Valle del Belice sheep.

A specific DNA duplication in Polish chickens affects feather shape by altering gene expression.

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

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

The research suggests that autophagy-related genes might play a role in causing alopecia areata.

The LncRNA AC010789.1 slows down hair loss by promoting hair follicle growth and interacting with miR-21 and the Wnt/β-catenin pathway.

ARHGEF3 is essential for proper hair follicle development in mice.

CLE14 peptide promotes root hair growth in Arabidopsis.

The Fas/FasL pathway may play a role in alopecia areata.

The KRTAP36-1 gene affects wool quality in Chinese Tan lambs.

Researchers found a new gene, hacl-1, that is active in mouse hair follicles during hair growth and may be important for hair biology.

AIRE deficiency causes hair loss similar to alopecia areata in mice.