Pages that link to "Q319812"
Jump to navigation
Jump to search
The following pages link to abetalipoproteinemia (Q319812):
Displaying 50 items.
- MTTP (Q18029579) (← links)
- Abetalipoproteinemia: two case reports and literature review (Q21202911) (← links)
- Absence of microsomal triglyceride transfer protein in individuals with abetalipoproteinemia (Q24294711) (← links)
- Molecular and functional analysis of two new MTTP gene mutations in an atypical case of abetalipoproteinemia (Q24301635) (← links)
- Novel missense MTTP gene mutations causing abetalipoproteinemia (Q24301849) (← links)
- Loss of both phospholipid and triglyceride transfer activities of microsomal triglyceride transfer protein in abetalipoproteinemia (Q24323872) (← links)
- Novel Abetalipoproteinemia Missense Mutation Highlights the Importance of the N-Terminal β-Barrel in Microsomal Triglyceride Transfer Protein Function (Q24338622) (← links)
- Decreased fluidity of red cell membrane lipids in abetalipoproteinemia (Q24595286) (← links)
- Molecular characterization of Tunisian families with abetalipoproteinemia and identification of a novel mutation in MTTP gene (Q24632454) (← links)
- Mutations of the microsomal triglyceride-transfer-protein gene in abetalipoproteinemia (Q24671906) (← links)
- Microsomal triglyceride transfer protein (MTP) gene mutations in Canadian subjects with abetalipoproteinemia (Q28145038) (← links)
- Abetalipoproteinemia is caused by defects of the gene encoding the 97 kDa subunit of a microsomal triglyceride transfer protein (Q28249803) (← links)
- Cloning and gene defects in microsomal triglyceride transfer protein associated with abetalipoproteinaemia (Q28262033) (← links)
- Vitamin E and neurological function: abetalipoproteinaemia and other disorders of fat absorption (Q28270346) (← links)
- The abetalipoproteinemia gene is a member of the vitellogenin family and encodes an α–helical domain (Q28296730) (← links)
- A novel abetalipoproteinemia genotype. Identification of a missense mutation in the 97-kDa subunit of the microsomal triglyceride transfer protein that prevents complex formation with protein disulfide isomerase (Q28298010) (← links)
- Vitamin E and Neurological Function: Abetalipoproteinaemia and Other Disorders of Fat Absorption (Q30040601) (← links)
- Abetalipoproteinemia-like lipid profile and acanthocytosis in a young woman with anorexia nervosa (Q33345441) (← links)
- Oral vitamin E supplements can prevent the retinopathy of abetalipoproteinaemia (Q33645105) (← links)
- The role of the microsomal triglygeride transfer protein in abetalipoproteinemia (Q33913539) (← links)
- Primary deficiency of microsomal triglyceride transfer protein in human abetalipoproteinemia is associated with loss of CD1 function (Q34028751) (← links)
- The lipoproteins and lipid transport in abetalipoproteinemia (Q34081229) (← links)
- Rickets and dysmorphic findings in a child with abetalipoproteinemia (Q34144227) (← links)
- A severe form of abetalipoproteinemia caused by new splicing mutations of microsomal triglyceride transfer protein (MTTP). (Q34169991) (← links)
- Ataxia with vitamin E deficiency and abetalipoproteinemia (Q34206840) (← links)
- Molecular and metabolic basis for the metabolic disorder normotriglyceridemic abetalipoproteinemia (Q34210824) (← links)
- Studies on the absorptive defect for triglyceride in abetalipoproteinemia (Q34266336) (← links)
- Peroxidative Hemolysis of Red Blood Cells from Patients with Abetalipoproteinemia (Acanthocytosis)* (Q34267365) (← links)
- Abnormalities of High Density Lipoproteins in Abetalipoproteinemia* (Q34270005) (← links)
- Arrest of neuropathy and myopathy in abetalipoproteinemia with high-dose vitamin E therapy (Q34300619) (← links)
- Novel mutations in SAR1B and MTTP genes in Tunisian children with chylomicron retention disease and abetalipoproteinemia (Q34304424) (← links)
- Abetalipoproteinemia. New insights into lipoprotein assembly and vitamin E metabolism from a rare genetic disease (Q34351859) (← links)
- Abetalipoproteinemia: importance of the peripheral blood smear (Q34402531) (← links)
- A study of the abnormal lipoproteins in abetalipoproteinemia (Q34461391) (← links)
- Epitopes of apolipoprotein B-100 and B-48 in both liver and intestine. Expression and evidence for local synthesis in recessive abetalipoproteinemia (Q34547554) (← links)
- Analysis of the apolipoprotein B gene and messenger ribonucleic acid in abetalipoproteinemia (Q34551885) (← links)
- Abetalipoproteinemia in Israel: evidence for a founder mutation in the Ashkenazi Jewish population and a contiguous gene deletion in an Arab patient (Q34574677) (← links)
- A successful spontaneous pregnancy in abetalipoproteinemia: Amsterdam or the art of vitamin replacement? (Q34691979) (← links)
- Long-term management of abetalipoproteinaemia. Possible role for vitamin E (Q34989797) (← links)
- Exclusion of linkage between the human apolipoprotein B gene and abetalipoproteinemia (Q35198378) (← links)
- Genetic evidence from two families that the apolipoprotein B gene is not involved in abetalipoproteinemia (Q35593754) (← links)
- Hypobetalipoproteinemia and abetalipoproteinemia (Q35738368) (← links)
- Extreme Contrast of Postprandial Remnant-Like Particles Formed in Abetalipoproteinemia and Homozygous Familial Hypobetalipoproteinemia (Q35801021) (← links)
- Knockout of the abetalipoproteinemia gene in mice: reduced lipoprotein secretion in heterozygotes and embryonic lethality in homozygotes. (Q36212658) (← links)
- Hormone changes during the menstrual cycle in abetalipoproteinemia: reduced luteal phase progesterone in a patient with homozygous hypobetalipoproteinemia (Q36319274) (← links)
- Regulation of cholesterol synthesis by low density lipoprotein in isolated human lymphocytes. Comparison of cells from normal subjects and patients with homozygous familial hypercholesterolemia and abetalipoproteinemia (Q36335476) (← links)
- Fat-soluble vitamin deficiency in pregnancy: a case report and review of abetalipoproteinemia. (Q36615326) (← links)
- Abetalipoproteinemia (author's transl) (Q36661368) (← links)
- Clinical utility gene card for: Abetalipoproteinaemia--Update 2014. (Q36695239) (← links)
- Role of Apolipoprotein E-containing Lipoproteins in Abetalipoproteinemia (Q36988305) (← links)