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1. PIK3CA inhibition in models of proliferative glomerulonephritis and lupus nephritis

3. A wave of deep intronic mutations in X-linked Alport syndrome

5. A monocyte/dendritic cell molecular signature of SARS-CoV-2-related multisystem inflammatory syndrome in children with severe myocarditis

6. Modeling the critical MCOR-causing deletion in mouse unveils aberrantSox21expression in developing and adult iris and ciliary body, and implicatesTgfβ2in MCOR-associated glaucoma and myopia

7. EFL1 mutations impair eIF6 release to cause Shwachman-Diamond syndrome

8. Mutations in PERP Cause Dominant and Recessive Keratoderma

9. Corrigendum: Human C-terminal CUBN variants associate with chronic proteinuria and normal renal function

10. ADCK4 mutations promote steroid-resistant nephrotic syndrome through CoQ10 biosynthesis disruption

11. Germline HAVCR2 mutations altering TIM-3 characterize subcutaneous panniculitis-like T cell lymphomas with hemophagocytic lymphohistiocytic syndrome

12. MINPP1 prevents intracellular accumulation of the chelator inositol hexakisphosphate and is mutated in Pontocerebellar Hypoplasia

13. A Variety of Alu-Mediated Copy Number Variations Can Underlie IL-12Rβ1 Deficiency

15. Targeted therapy in patients with PIK3CA-related overgrowth syndrome

16. Recessive loss of function PIGN alleles, including an intragenic deletion with founder effect in La Réunion Island, in patients with Fryns syndrome

17. An in vivo genetic reversion highlights the crucial role of Myb-Like, SWIRM, and MPN domains 1 (MYSM1) in human hematopoiesis and lymphocyte differentiation

20. Frequent Alterations of Driver Genes in Chromosome X and Their Clinical Relevance in Extranodal NK/T-Cell Lymphoma

21. Neuropathological hallmarks of antenatal mitochondrial diseases with a corpus callosum defect

22. Recurrent KIF2A mutations are responsible for classic lissencephaly

23. Immune deficiency–related enteropathy-lymphocytopenia-alopecia syndrome results from tetratricopeptide repeat domain 7A deficiency

27. Targeted Exome Sequencing Identifies PBX1 as Involved in Monogenic Congenital Anomalies of the Kidney and Urinary Tract

29. Neuropathological hallmarks of antenatal mitochondrial diseases with a corpus callosum defect.

31. Human C-terminal CUBN variants associate with chronic proteinuria and normal renal function

33. A rare castration‐resistant progenitor cell population is highly enriched in Pten‐null prostate tumours

34. Mutations in BOREALIN cause thyroid dysgenesis

36. Author Correction: Targeted therapy in patients with PIK3CA-related overgrowth syndrome

37. Author Correction: Germline HAVCR2 mutations altering TIM-3 characterize subcutaneous panniculitis-like T cell lymphomas with hemophagocytic lymphohistiocytic syndrome

42. A human immunodeficiency caused by mutations in the PIK3R1 gene

43. TTC7A mutations disrupt intestinal epithelial apicobasal polarity

44. Prenatal‐onset of congenital neuronal ceroid lipofuscinosis with a novel CTSD mutation

46. B cell depletion in immune thrombocytopenia reveals splenic long-lived plasma cells

49. Onset of autoimmune lymphoproliferative syndrome (ALPS) in humans as a consequence of genetic defect accumulation

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