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Patients with a specific genetic variant have more severe alopecia areata and higher recurrence rates.

Certain genetic markers can indicate a person's risk of developing prostate cancer.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

The CRABP I gene in cashmere goats is highly conserved but has unique features at specific amino sites.

The ABCG2 gene variant increases the risk of high uric acid and cholesterol, especially in overweight or obese young Mexican males.

A certain genetic variation in the IL1A gene may lower the risk of a hair loss condition in Chinese people.

A specific gene variation in goats is linked to better growth traits.

CENPV, a new partner of CYLD, helps regulate ciliary acetylated tubulin and is overexpressed in certain skin tumors.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

Hereditary hyperplastic gingivitis in silver foxes may be linked to errors in the MAPK signaling pathway, influenced by androgens.

The study found that a specific genetic variation in the TNFα gene is significantly linked to Alopecia Areata in the Jordanian Arab population.

The gene Prss53 affects hair shape and bone development in rabbits.

New genetic variants linked to albinism were found in Pakistani families.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

New mutations in the EBP gene cause CDPX2, affecting bones, skin, eyes, and hair, with females generally less affected than males.

Removing anthrax toxin receptor 1 in pigs prevents Senecavirus A infection and causes a rare disease similar to GAPO syndrome.

Some canine hair follicle tumors contain amyloid deposits, with a protein called CK5 involved in their formation.

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

Four new FGF5 gene variants cause long hair in dogs.

The MTHFR C677T mutation may increase the risk of alopecia areata in the Turkish population.

Different types of androgens bind differently to two receptors, AR1 and AR2, in Atlantic croaker's brain and ovarian tissues, suggesting these receptors may control different androgen actions in fish.

Agouti protein affects melanocortin receptors through competitive antagonism and receptor down-regulation.

A gene called Taqpep affects cat coat patterns like stripes and blotches.

Noggin gene inactivation causes skeletal defects in mice, varying by genetic background.

Common variants in the Trichohyalin gene are linked to straight hair in Europeans.

Certain DNA variants can predict straight hair in Europeans but are not highly specific.

The HGCA tool helps identify genes that work together by analyzing their co-expression patterns.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.