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The study identified and characterized new keratin genes linked to hair follicles and epithelial tissues.

Certain genetic markers on chromosome 20 are linked to hair loss in the Han Chinese from Yunnan.

The research concluded that selection significantly shaped the genetic variation of the X chromosome, with certain regions affected by past selective events.

Identical twins had different symptoms because one had more cells with an extra chromosome fragment in different tissues.

Acute leukemias with the Philadelphia chromosome may be biphenotypic, and identifying this is important for proper treatment.

A six-year-old boy with excessive hair growth and other symptoms may have a genetic link on chromosome 17q, requiring regular medical follow-ups.

Keratosis Follicularis Spinulosa Decalvans is a rare genetic disorder causing skin and hair issues, often inherited through the X chromosome.

Alopecia areata involves both innate and adaptive immunity, with specific genes linked to the disease.

Mutations in the P2RY5 gene cause autosomal recessive woolly hair.

Certain genes on chromosomes 6, 10, 16, and 18 may increase the risk of alopecia areata.

Researchers found a new gene area linked to male-pattern baldness, which, along with another gene, significantly increases the risk of hair loss in men.

Alopecia areata is likely caused by a combination of genetic factors and immune system dysfunction, and may represent different diseases with various causes.

Mice with the 'lanceolate hair' mutation have abnormal hair and skin similar to human Netherton's syndrome.

Two specific hair keratin genes are active during hair growth and decline as hair transitions to rest.

The document concludes that more multidisciplinary research is needed to understand and treat PCOS, a condition that significantly affects women's health and quality of life.

Sheep have a unique gene, KAP8-2, that humans don't have, which may affect wool properties.

New treatments for alopecia areata may target specific immune cells and pathways involved in hair loss.

Researchers found two genes that may explain why some Casertana pigs don't have hair.

Hair microscopy is useful for diagnosing hair disorders, but clear definitions are needed for accurate genetic analysis.

Accurate diagnosis of APL is crucial to avoid unnecessary treatments.

The study found nine new hair protein genes in human hair follicles.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

A 12-year-old boy with a rare genetic condition has progressive hair loss with no effective treatment.

An Australian with rare hair loss and eye conditions had a gene linked to both, not seen together before.

Two specific genetic markers increase the risk of hair loss in Asian populations.

Frontal Fibrosing Alopecia is a hair loss condition mainly affecting postmenopausal women, with unclear causes and various clinical patterns.

A teenager's hair with alternating white and dark bands, known as Pili annulati, is a genetic condition that is usually harmless and often considered attractive.

A girl inherited excessive body hair from her mother and grandmother.

Environmental factors like smoking, UV exposure, and poor diet contribute to hair loss and graying, and lifestyle changes can help manage it.

Certain genes are linked to the risk of developing Alopecia Areata.