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A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

Certain genetic markers on the Y-chromosome may influence prostate cancer risk in Iraqi males.

Monilethrix is linked to the type II keratin gene on chromosome 12q13.

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

Björnstad syndrome causes twisted hair from birth.

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

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

The condition is linked to chromosome 12, but no mutations were found in the known genes.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

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

Some people with schwannomatosis have a new type of mutation in the LZTR1 gene.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

A specific genetic deletion in goats affects cashmere yield and thickness.

SLE is likely one disease with various symptoms, not multiple distinct diseases.

The study found genetic variations in sheep linked to traits like milk production, growth, and health.

Acidic keratin genes are on CFA9 and basic keratin genes are on CFA27 in dogs.

SNP rs2479106 in the DENND1A gene may increase PCOS risk in Saudi Arabian females.

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

Seven new genetic risk areas for prostate cancer were found.

Crossbreeding certain European cattle breeds may cause hair and physical issues in cattle.

A 19-month-old Saudi girl had a rare skin condition with no other defects, and her family was unaffected.

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

A specific gene mutation causes long hair in Angora rabbits.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.

Cantú syndrome may be linked to pituitary adenomas.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

Growth hormone therapy can improve growth in Netherton syndrome patients with growth hormone deficiency.

Combining genetic and physical data improves diagnosis and treatment for early-onset monogenic diabetes.

The peach gene CTG134 helps control the interaction between auxin and ethylene, which could lead to new agricultural chemicals.