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Four antibodies were developed to help study hair follicle cell differentiation.

The boy's genetic diagnosis of ectodermal dysplasia helped improve management and counseling for him and his sister.

The skin's basement membrane is specially designed to support different types of connections between skin layers and hair follicles.

OsUEV1B protein is essential for controlling phosphate levels in rice.

Mutations in the LSS gene cause hair loss and may affect brain development, with varying severity.

The EDA pathway plays a key role in bone development by interacting with other signaling pathways.

The research found specific proteins that affect fiber characteristics and hair growth in sheep and goats.

A new, efficient method creates sulfinimidate esters from sulfenamides and alcohols without metals.

Researchers found a non-functional sheep keratin gene due to mutations.

The Cashmere goat hair keratin gene is crucial for hair structure.

New mutations in hair keratin genes cause the rare hair disorder monilethrix.

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

Epidermolytic ichthyosis can be inherited in a semidominant way with mild symptoms in carriers.

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

The POMP gene is active in various goat tissues and affects hair growth, with certain treatments influencing its expression.

Minoxidil analogs can be improved for hair growth inhibition by modifying specific parts of their structure.

Mutations in the RBPJ gene cause Adams-Oliver Syndrome.

The research identified six functional hair keratin genes and four pseudogenes, providing insights into hair formation and gene organization.

A defective gene causes hair loss and taste insensitivity in BTBR mice.

Identical twins with a rare KRT 86 gene mutation both have the hair disorder monilethrix.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

Researchers found genes and genetic variants linked to sheep wool and skin wrinkles.

The document confirms the structures of major metabolites of the CRTh2 antagonist Setipiprant and identifies minor metabolites.

Differences in cashmere quality between goat breeds are linked to specific genes affecting hair follicle development.

A new genetic mutation in the TRPV3 gene causes Olmsted-like syndrome in a Mongolian family.

Researchers created a genetic library from a cashmere goat's skin and found new genes linked to hair growth.

Deleting Snai2 and Snai3 causes fatal autoimmunity.

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