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Changing light exposure can affect hair growth timing in goats, possibly due to a key gene, CSDC2.

Molecular diagnostics help identify genetic defects causing endocrine diseases, improving diagnosis and treatment options.

Hoxc13 gene affects wool length in Gansu alpine fine-wool sheep.

The peach gene pCTG134 helps control the interaction between auxin and ethylene hormones during fruit ripening.

Eyelid cells share signaling components but differ in pathway activity.

Bald thigh syndrome in sighthounds is caused by structural defects in hair shafts due to downregulated genes and proteins.

Hair follicles have a more inactive cell cycle than other skin cells, which may help develop targeted therapies for skin diseases and cancer.

Vitamin D affects Msx1 protein expression and may influence mineralized tissue health.

Deleting MED1 in skin cells causes hair loss and skin changes.

Claudin expression changes help the skin respond to injury.

Loss of Msx2 function causes eye development issues similar to Peters anomaly.

Certain gene mutations can weaken the skin barrier and, when combined with environmental factors, lead to eczema and severe itching.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

The Foxn1 gene mutation causes hairlessness and immune system issues, and understanding it could lead to hair growth disorder treatments.

Mice without the vitamin D receptor gene lose hair due to disrupted hair follicle cycles.

HOXC13 is essential for hair and nail development by regulating Foxn1.

Mice with extra human KLK14 had hair and skin problems, including weaker cell bonds and inflammation, linked to Netherton syndrome.

The Msx2 gene affects feather development in Hungarian white geese and a specific gene variation could indicate feather quality.

SP1 promotes and KROX20 inhibits hair cell growth by affecting the CUX1 gene.

The research shows that a gene called Wnt3 affects hair growth and structure, causing short hair and balding when overactive.

A WNT10A gene mutation leads to ectodermal dysplasia by disrupting cell growth and differentiation.

FOXN1 gene variants cause low T cells and immune issues from birth.

Ultrasound can help deliver genes to cells to stimulate tissue regeneration and enhance hair growth, but more research is needed to perfect the method.

DNA methylation likely doesn't cause different lambskin patterns in Hu sheep.

A mutation in the KRT82 gene is significantly associated with Alopecia Areata.

The Hairless gene is crucial for healthy skin and hair growth.

The tumor suppressor gene FLCN affects mitochondrial function and energy use in cells.

Mice without active or present vitamin D receptors maintain normal blood sugar control and islet gene expression when calcium levels are normal.

The TRPV3 ion channel is important for skin and hair health and could be a target for treating skin conditions.

Meis2 is essential for touch sensation and proper nerve connection to touch receptors in certain skin areas of mice.