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Testing for CAG repeat polymorphism in the androgen receptor gene is not currently recommended for managing hypogonadism.

Certain human skin cells marked by CD44 and ALDH are rich in stem cells capable of long-term skin renewal.

lncRNA XLOC_008679 and gene KRT35 affect cashmere fineness in goats.

Researchers created a mouse model of a type of rickets that does not cause hair loss.

PCOS may start before birth, involves metabolic issues, and can be treated with drugs like metformin and lifestyle changes.

Short-term finasteride treatment may lower some cell death factors in prostate cancer cells.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

Nellore cattle have genetic variations linked to their adaptation to tropical environments.

Amenorrhea, or the absence of periods, should be evaluated by age 15 or within five years of early breast development, and is most commonly caused by conditions like polycystic ovary syndrome and hypothalamic amenorrhea.

The research identified genes and pathways important for sheep wool growth and shedding.

Patients with myotonic dystrophy often have skin problems that suggest early aging and vitamin D issues, and the severity of these problems is linked to their genetic condition and vitamin D levels.

Alopecia areata causes hair loss due to an immune attack on hair follicles, influenced by genetics and environment.

Nanog gene boosts stem cells, helps hair growth, and may treat hair loss.

The transition from growth to regression in Cashmere goat hair follicles involves changes in expression of genes related to keratin and cell differentiation.

The extract from Bacillus/Trapa japonica fruit helps increase hair growth and could be a potential treatment for hair loss.

A mutation in the FAM83G gene is linked to skin and hair abnormalities in two related individuals.

Malassezia yeast linked to hair loss; ketoconazole helps treat it.

A new mutation in the AGPAT2 gene causes severe fat tissue loss and related health issues by reducing the protein's levels.

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.

An 11-year-old Greek girl was diagnosed with a rare genetic disorder, highlighting the importance of genetic testing and family history.

5α-reductase inhibitors can interfere with doping tests by masking banned substances.

The conclusion is that lifestyle changes and weight loss are first-line treatments for infertility due to anovulation, with various medications and assisted reproductive technologies as additional options.

Humans have limited regenerative abilities, but new evidence shows the adult brain and heart can regenerate, and future treatments may improve this by mimicking stem cell environments.

Low-coverage sequencing is a cost-effective way to identify genes related to wool traits in rabbits.

Dermatopathology has made significant progress but many skin diseases remain incurable, requiring ongoing research.

Reduced alpha smooth muscle actin may cause hair loss in androgenetic alopecia.

There is no cure for myotonic dystrophy type 1, so treatment focuses on managing symptoms and complications.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

Diagnosing sex development disorders requires combining medical history, physical exams, imaging, lab tests, and genetic data.

The SbbHLH85 protein helps sweet sorghum grow more root hairs but makes the plant more sensitive to salt.