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2. Mutations of GEMIN5 are associated with coenzyme Q10 deficiency: long-term follow-up after treatment

4. LSD1/PRMT6-targeting gene therapy to attenuate androgen receptor toxic gain-of-function ameliorates spinobulbar muscular atrophy phenotypes in flies and mice

5. WNK kinases sense molecular crowding and rescue cell volume via phase separation

9. MATR3 pathogenic variants differentially impair its cryptic splicing repression function

10. Loss of function mutations in GEMIN5 cause a neurodevelopmental disorder

11. Dual Inhibition of GSK3β and CDK5 Protects the Cytoskeleton of Neurons from Neuroinflammatory-Mediated Degeneration In Vitro and In Vivo

12. Differential effects of MATR3 variants on its cryptic splicing repression function

13. Drosha-dependent microRNAs modulate FUS-mediated neurodegeneration in vivo

15. Nuclear-Import Receptors Reverse Aberrant Phase Transitions of RNA-Binding Proteins with Prion-like Domains

16. Isogenic FUS-eGFP iPSC Reporter Lines Enable Quantification of FUS Stress Granule Pathology that Is Rescued by Drugs Inducing Autophagy

17. FUS pathology in ALS is linked to alterations in multiple ALS-associated proteins and rescued by drugs stimulating autophagy

20. NgR1 binding to reovirus reveals an unusual bivalent interaction and a new viral attachment protein

21. Axon guidance genes modulate neurotoxicity of ALS-associated UBQLN2

23. Mutations of GEMIN5 are associated with coenzyme Q10deficiency: long-term follow-up after treatment

24. Muscleblind acts as a modifier of FUS toxicity by modulating stress granule dynamics and SMN localization

27. Protein Arginine Methyltransferase 6 Enhances Polyglutamine-Expanded Androgen Receptor Function and Toxicity in Spinal and Bulbar Muscular Atrophy

28. Axon guidance pathways modulate neurotoxicity of ALS-associated UBQLN2

30. Further delineation of GEMIN4 related neurodevelopmental disorder with microcephaly, cataract, and renal abnormalities syndrome

32. Functional and structural deficiencies of Gemin5 variants associated with neurological disorders

35. Functional and structural deficiencies of Gemin5 variants associated with neurological disorders

37. Autosomal Recessive Cerebellar Atrophy and Spastic Ataxia in Patients With Pathogenic Biallelic Variants in GEMIN5

38. WNK kinases sense molecular crowding and rescue cell volume via phase separation

39. Traumatic injury compromises nucleocytoplasmic transport and leads to TDP-43 pathology

40. Author response: Traumatic injury compromises nucleocytoplasmic transport and leads to TDP-43 pathology

41. HDAC6 rescues neurodegeneration and provides an essential link between autophagy and the UPS

42. Polyglutamine-Expanded Androgen Receptor Alteration of Skeletal Muscle Homeostasis and Myonuclear Aggregation Are Affected by Sex, Age and Muscle Metabolism

47. Polyglutamine-Expanded Androgen Receptor Alteration of Skeletal Muscle Homeostasis and Myonuclear Aggregation Are Affected by Sex, Age and Muscle Metabolism

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