Pages that link to "Q28318565"
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The following pages link to Multiple biotin-dependent carboxylase deficiencies associated with defects in T-cell and B-cell immunity (Q28318565):
Displaying 50 items.
- Biotin (Q28026625) (← links)
- Office evaluation of children with recurrent infection (Q34114524) (← links)
- Biotinidase deficiency: a novel vitamin recycling defect (Q34195645) (← links)
- Biotin in clinical medicine—a review (Q34246416) (← links)
- Biotin biochemistry and human requirements (Q34366995) (← links)
- Biotin deficiency induces changes in subpopulations of spleen lymphocytes in mice (Q34745919) (← links)
- The syndrome of chronic mucocutaneous candidiasis with selective antibody deficiency (Q35071964) (← links)
- Inherited disorders of 3-methylcrotonyl CoA carboxylation (Q35114768) (← links)
- Heterogeneity of holocarboxylase synthetase in patients with biotin-responsive multiple carboxylase deficiency (Q35200249) (← links)
- Biochemical characterization of biotin-responsive multiple carboxylase deficiency: heterogeneity within the bio genetic complementation group. (Q35201707) (← links)
- The biotin-dependent carboxylase deficiencies (Q35202451) (← links)
- Mutant holocarboxylase synthetase: evidence for the enzyme defect in early infantile biotin-responsive multiple carboxylase deficiency (Q37006348) (← links)
- Epigenetic synergies between biotin and folate in the regulation of pro-inflammatory cytokines and repeats. (Q37281012) (← links)
- Antenatal and postnatal radiologic diagnosis of holocarboxylase synthetase deficiency: a systematic review (Q38692773) (← links)
- Lipopolysaccharide inhibits colonic biotin uptake via interference with membrane expression of its transporter: a role for a casein kinase 2-mediated pathway (Q38722967) (← links)
- Nutrition and autoimmunity: a review (Q39748211) (← links)
- Effects of specific nutrients on the immune response. Selected clinical applications (Q39849601) (← links)
- Metabolic Diseases and the Skin (Q40091186) (← links)
- Vitamin-Responsive Inborn Errors of Metabolism (Q40096951) (← links)
- The biochemical basis of immunodeficiency disease (Q40122979) (← links)
- Metabolic defects in immunodeficiency diseases. (Q40131415) (← links)
- Propionic acidemia: a clinical update (Q40320371) (← links)
- Nutrition Classics. The Journal of Biological chemistry, 39:3808-17, 1964. The importance of both synthesis and degradation in the control of arginase levels in rat liver. Robert T. Schimke (Q41160225) (← links)
- Role of the sodium-dependent multivitamin transporter (SMVT) in the maintenance of intestinal mucosal integrity (Q41546041) (← links)
- Biotin deficiency enhances the inflammatory response of human dendritic cells. (Q42361270) (← links)
- Mutations in the Human Biotinidase Gene That Cause Profound Biotinidase Deficiency in Symptomatic Children: Molecular, Biochemical, and Clinical Analysis (Q45108302) (← links)
- Clinical features and diagnostic approach in type I tyrosinaemia in an infant with cytomegaly virus infection and bacterial sepsis (Q45775374) (← links)
- Integrated Omic Analysis of a Guinea Pig Model of Heart Failure and Sudden Cardiac Death. (Q46539324) (← links)
- Organic aciduria in late-onset biotin-responsive multiple carboxylase deficiency. (Q54495450) (← links)
- Biotin Deficiency Induces Th1- and Th17-Mediated Proinflammatory Responses in Human CD4+ T Lymphocytes via Activation of the mTOR Signaling Pathway. (Q55421717) (← links)
- Characterization and functional analysis of cellular immunity in mice with biotinidase deficiency (Q58966944) (← links)
- Multiple biotin-dependent carboxylase deficiencies associated with defects in immunity (Q66898218) (← links)
- Abnormal fatty acid composition of biotin-responsive multiple carboxylase deficiency fibroblasts (Q69213339) (← links)
- Biotinidase deficiency associated with severe combined immunodeficiency (Q69371782) (← links)
- [Reduction of biotin level as a possible factor in the mode of action of anticonvulsants (author's transl)] (Q70304173) (← links)
- Immune functions in methylmalonicaciduria (Q70485826) (← links)
- Biotin dependent multiple carboxylase deficiency presenting as a congenital lactic acidosis (Q70670228) (← links)
- The neonatal form of biotin-responsive multiple carboxylase deficiency (Q70878647) (← links)
- Biotin-responsive multiple carboxylase deficiency of infantile onset (Q70878651) (← links)
- Megavitamin therapy in inherited metabolic disorders (Q71065954) (← links)
- Holocarboxylase synthetase deficiency: a biotin-responsive organic acidemia (Q71162249) (← links)
- Two forms of biotin-responsive multiple carboxylase deficiency (Q71564023) (← links)
- Biotin-responsive in vivo carboxylase deficiency in two siblings with secretory diarrhea receiving total parenteral nutrition (Q71567786) (← links)
- Biochemical evidence for diverse etiologies in biotin-responsive multiple carboxylase deficiency (Q71608746) (← links)
- Organic aciduria in neonatal multiple carboxylase deficiency (Q71646880) (← links)
- Phenotypic variation in biotinidase deficiency (Q71799020) (← links)
- Biotin deficiency with neurologic and cutaneous manifestations but without organic aciduria (Q71799041) (← links)
- Alopecia and periorificial dermatitis in biotin-responsive multiple carboxylase deficiency (Q71830533) (← links)
- Autosomal dominant transmission and absence of HLA linkage in dexamethasone suppressible hyperaldosteronism (Q72420551) (← links)
- Propionacidaemia and immunodeficiency (Q72420553) (← links)