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Nanotechnology is improving drug delivery and targeting, with promising applications in cancer treatment, gene therapy, and cosmetics, but challenges remain in ensuring precise delivery and safety.

Hair analysis can show nutritional status and environmental exposure, with phosphorus being very stable in hair and differences found based on gender and conditions like depression and autism.

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

The length of CAG repeats in the androgen receptor gene is linked to ovarian reserve but does not affect how the ovaries respond to stimulation.

Using special RNA to target a mutant gene fixed hair problems in mice.

Certain gene patterns in breast cancer are linked to how active hormone receptors are and could affect patient survival.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

Newborn screening and gene therapy are expected to improve outcomes for Omenn syndrome patients.

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

The congress highlighted new gene therapy techniques and cell transplantation methods for treating diseases.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

The conclusion is that the nuclear lamina and LINC complex in skin cells respond to mechanical signals, affecting gene expression and cell differentiation, which is important for skin health and can impact skin diseases.

The peach gene pCTG134 helps control the interaction between auxin and ethylene hormones during fruit ripening.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

A genetic change in the EDAR gene causes the unique hair traits found in East Asians.

Mice without the vitamin D receptor gene lose hair due to disrupted hair follicle cycles.

The conclusion is that recognizing hair growth cycles can improve the precision of dietary and health assessments from hair analysis.

Hair loss gene found on chromosome 3q26.

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

The gene for slick hair in Senepol cattle is located on chromosome 20 and may involve the SRD5A2 gene.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

Certain HSD3B1 gene types are linked to worse prostate cancer outcomes and affect treatment response and other health conditions.

The gene p53 is crucial for removing damaged cells to allow for healthy tissue renewal.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

The study concludes that mutations in the AEBP1 gene can cause a form of Ehlers-Danlos syndrome and should be considered in diagnosis.

A gene called Gk5 controls lipid production in the skin and affects hair growth.

A boy's growth and immune problems were caused by a new mutation in the STAT5B gene.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

Vitamin D receptor can control the hairless gene linked to hair loss even without vitamin D.

Certain gene variations increase the risk of alopecia areata in Koreans.