Somatic mutation analysis is a standard of practice for tumors in order to identify therapeutic sensitizing and resistance mutations. This allows a finer assessment of the diagnosis and prognosis and targeted therapies directed towards the individual patients tumor profile.
The global Somatic Genetic Testing market was valued at US$ million in 2023 and is anticipated to reach US$ million by 2030,...
Alpha-fetoprotein (AFP) is the most common plasma protein produced by the liver of a fetus. When a baby is born, AFP levels are usually high; however, the level falls to quite low by age one. It is necessary for a healthy adult to have very low levels of AFP. Alpha-fetoprotein (AFP) tumor marker is used to detect and diagnose cancer of the liver, testicles, and ovaries. A blood sample is required...
Wolfram syndrome is an inherited condition characterized by the childhood onset of diabetes mellitus, diabetes insipidus, and optic atrophy, causing gradual loss of vision and deafness
Wolfram syndrome is a rare neurodegenerative disease that is considered as a prototype of the endoplasmic reticulum disease. There are two identified causative agents, WFS1 and WFS2, responsible for Wolfram syndrome...
Buerger's disease is a rare disease of the arteries and veins in the arms and legs. It is also called as thromboangiitis obliterans. In Buerger's disease, the blood vessels become inflamed, swell, and get blocked due to blood clots.
The global Buerger Disease Diagnosis market was valued at US$ million in 2023 and is anticipated to reach US$ million by 2030, witnessing a CAGR of % during the forec...
Among the clinical uses of flow cytometry cancer represents one of the most relevant. Several applications of flow cytometry can currently be applied to the study of cancer, including the detection of tumour cell DNA aneuploidy, the analysis of tumour cell proliferation and the immunophenotyping of leukemias.
The global Flow Cytometry in Oncology market was valued at US$ million in 2023 and is an...
Gene therapy (gene therapy) refers to the introduction of foreign normal genes into target cells to correct or compensate for diseases caused by defects and abnormal genes in order to achieve therapeutic purposes. It also includes the application of technology such as transgenes, that is, inserting foreign genes into appropriate recipient cells of patients through gene transfer technology, so that...
In prenatal diagnosis, genetic counseling is a process of obtaining marriage and childbearing recommendations through diagnosis and evaluation, to reduce the probability of birth of children with genetic diseases
The global Genetic Counseling market was valued at US$ million in 2023 and is anticipated to reach US$ million by 2030, witnessing a CAGR of % during the forecast period 2024-2030.
Nort...
Ocular hypertension is caused by poor drainage of the fluid inside the eye. Essentially, this means that too much fluid enters the eye without being drained, causing high amount of pressure to build up.
The global Ocular Hypertension Treatment market was valued at US$ million in 2023 and is anticipated to reach US$ million by 2030, witnessing a CAGR of % during the forecast period 2024-2030.
The...
Erythropoietic protoporphyria (EPP) is a rare inherited metabolic disorder caused by a deficiency of the enzyme ferrochelatase (FECH), which results from changes (mutations) in the FECH gene. Due to abnormally low levels of this enzyme, excessive amounts of protoporphyrin accumulate in the bone marrow, blood plasma, and red blood cells. Some patients with symptoms of EPP have a genetic change in a...
As per the International Federation of Pharmaceutical Manufacturers & Associations, out of the total expenditure on drug discovery, 25% is spent on preclinical testing. Implementation of single-domain antibodies for drug discovery saves money and shortens the very lengthy process, contributing to higher demand in the single-domain antibody platforms market.
The global Single-Domain Antibody Platf...
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