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Certain gene variations are linked to severe acne in Egyptian patients and could guide treatment choices.

A girl with a rare genetic disorder had a unique bone condition, highlighting the need for careful diagnosis and suggesting the disorder might be more common than thought.

A patient with a larger than usual genetic mutation had a broader range of symptoms for a muscle disease.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

Retinoic acid affects male and female muscle energy use and function differently.

A circular RNA helps cashmere goat hair cells become hair follicles by blocking a molecule to boost a gene important for hair growth.

Stress can cause a type of hair loss in mice lacking the CCHCR1 gene.

A mutation in the KRT75 gene causes frizzle feathers in chickens.

Increasing neurotrophin 4 in skin boosts nerve endings but not sensory neuron count.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

A mutation in the KRTHB5 gene causes hair and nail issues.

Certain genes are linked to the risk of developing Alopecia Areata.

Mouse touch-sensitive nerve cells adjust their connections based on competition with other similar cells.

R-spondin2 may help treat hair loss, gene differences could explain baldness, a peptide's regulation is linked to psoriasis, B-defensin gene copies may affect a skin condition's risk and severity, and potential markers and targets for alopecia areata were identified.

CARASIL can cause different symptoms even with the same genetic mutation.

A gene mutation in mice causes permanent hair loss and skin issues.

MG53 helps reduce skin damage caused by nitrogen mustard.

Mcl-1 can activate Wnt signaling in skin cells, promoting growth and possibly cancer.

Four circRNAs were found to be significantly different in cashmere goat skin, affecting cashmere fineness.

PlncRNA-1 helps hair follicle stem cells grow and develop by controlling a specific cell signaling pathway.

Gene regulatory regions evolve faster than protein coding regions, allowing new gene relationships without changing transcription factors.

LGR5 is a common marker of hair follicle stem cells in different animals and is important for hair growth and regeneration.

The Notch signaling pathway helps in mouse hair development through a noncanonical mechanism that does not rely on RBPj or transcription.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

Measuring minimal residual disease on day 15 helps identify high-risk leukemia patients.

A mutant FERONIA gene affects root hair growth at high temperatures.

ALRV5XR significantly improves hair density in women with hair loss and is well-tolerated.

Some people have genetic mutations that make them resistant to vitamin D, leading to rickets even with enough vitamin D intake.

The study suggests that a specific type of immune cell, memory-like NK cells, may increase during active hair loss in Alopecia areata.