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The combination of tadalafil and finasteride improves urinary symptoms and erectile function in men with enlarged prostates.

New genes linked to male pattern baldness were found on chromosome 20p11.

A cat's poor wound healing was linked to a genetic deletion in the COL5A1 gene.

The research found specific genes and proteins that affect how fast chickens' feathers grow, which is not solely determined by traditional inheritance patterns.

Cats with abnormal hair had DSG4 gene changes causing hair problems.

Hair follicles create different cell layers and proteins, controlled by various molecules.

The document concludes that recent research has improved understanding of skin diseases and the balance between cell growth and differentiation in the epidermis.

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

WNT10A mutations often cause ectodermal dysplasias, with males showing more tooth issues than females.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

Stem cell plasticity is crucial for wound healing but can also contribute to cancer development.

Mutations in three genes cause Uncombable Hair Syndrome, leading to frizzy hair that can't be combed flat.

New treatments targeting specific genes show promise for treating keratin disorders.

Giving a special protein to dogs with a certain genetic disease improved their symptoms but didn't help with hair growth.

Turing patterns are now recognized as important in developmental biology.

X-linked mental retardation includes various syndromes with both mental and physical abnormalities.

A new gene, JMJD1C, may affect testosterone levels in men.

A gene mutation in mice causes skin defects and early death.

Hair loss gene found on chromosome 3q26.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

Patients with Bohring-Opitz syndrome and ASXL1 mutations need regular kidney ultrasounds to check for tumors.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

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

Mutations in keratin genes cause cell fragility and various skin disorders.

Progerin affects cell shape but not hair or skin in mice.

Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.

A gene variation is linked to hair thickness in Asians.

The study found that males with KFSD had severe skin and eye symptoms, while female carriers had milder symptoms.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.