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Severe genetic variants in children with a specific adrenal condition match predicted symptoms well, but milder variants do not.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

A specific gene mutation in Japanese people can cause varying degrees of hair thinning in adulthood.

Low-coverage sequencing is a cost-effective way to find genetic factors affecting rabbit wool traits.

The most different genetic segment between Africans and East Asians is the EDA2R/AR region, with two main types influenced by population changes and natural selection, and linked to baldness.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

PolyQ repeats in neural proteins evolve together, affecting brain function and disease.

Certain variations of the HDAC9 gene can increase or decrease stroke risk in the Chinese population.

A common mutation in the hHb6 gene is linked to monilethrix, but other factors may also play a role.

Certain gene variations are linked to a higher risk of severe acne, suggesting a genetic influence on the condition.

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

New method finds genetic links between Type 2 Diabetes and Prostate Cancer not seen before.

Certain gene variations in PITX2 are linked to a higher risk of male pattern baldness in Indians.

Screening for the NUDT15 gene variant can prevent severe side effects from thiopurine drugs in East-Asian people.

Certain genetic markers may increase or decrease prostate cancer risk.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

Mutations in the HOXC13 gene cause hair and nail development issues.

Ablative fractional laser treatment nearly matches the gene reduction effects of topical vismodegib in skin cancer.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

Disabling the FGF5 gene in sheep leads to longer wool.

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

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

Overexpression of SSAT causes hair loss and skin issues, but reducing putrescine can help.

Injecting specific oligonucleotides can change hair growth and structure by altering a gene.

Schizophrenia risk genes may affect early brain development, contributing to the disease.

A specific gene variant may increase the risk of developing Alopecia Areata.

Four new FGF5 gene variants cause long hair in dogs.