63 results on '"Thakker, Rajesh"'
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2. GNAQ/GNA11 Mosaicism Is Associated with Abnormal Serum Calcium Indices and Microvascular Neurocalcification
3. Neurodevelopmental Abnormalities in Patients with Familial Hypocalciuric Hypercalcemia Type 3
4. Characterization of a novel radiation hardened by design (RHD14) bit-cell based on 20-nm FinFET technology using TCAD simulations
5. Corrigendum to ‘Multiple endocrine neoplasia type 1 in children and adolescents: Clinical features and treatment outcomes’ [Surgery 171 (2021) 77–87]
6. Whole Exome Sequencing in Two South-East Asian Families with Atypical Femur Fractures
7. Multiple endocrine neoplasia type 1 in children and adolescents: Clinical features and treatment outcomes
8. Medial Arterial Calcification
9. Familial Hypocalciuric Hypercalcemia Type 1 and Autosomal-Dominant Hypocalcemia Type 1: Prevalence in a Large Healthcare Population
10. Transmission Gate and Hybrid Cmos Full Adder Characterization and Power-Delay Product Estimation Based on Mathematical Model
11. Parameter Extraction of PSP MOSFET Model in Multi-core Zynq SoC Platform
12. Improving the performance of transmission gate and hybrid CMOS Full Adders in chain and tree structure architectures
13. Two Synchronous Pituitary Adenomas Causing Cushing Disease and Acromegaly
14. Molecular Genetic Studies of Pancreatic Neuroendocrine Tumors
15. Hybrid offset compensated latch-type sense amplifier for tri-gated FinFET technology
16. A near-threshold 10T differential SRAM cell with high read and write margins for tri-gated FinFET technology
17. AP2σ Mutations Impair Calcium-Sensing Receptor Trafficking and Signaling, and Show an Endosomal Pathway to Spatially Direct G-Protein Selectivity
18. Expression profiling of colorectal cancer cells reveals inhibition of DNA replication licensing by extracellular calcium
19. Allosteric Modulation of the Calcium-sensing Receptor Rectifies Signaling Abnormalities Associated with G-protein α-11 Mutations Causing Hypercalcemic and Hypocalcemic Disorders
20. Challenges and controversies in management of pancreatic neuroendocrine tumours in patients with MEN1
21. Discovering gene function from development to ageing
22. The calcium-sensing receptor: And its involvement in parathyroid pathology
23. Multiple endocrine neoplasia type 1 (MEN1) and type 4 (MEN4)
24. Rickets and osteomalacia
25. Multiple endocrine neoplasia
26. Calcium-sensing receptor (CaSR) mutations and disorders of calcium, electrolyte and water metabolism
27. In memoriam: Oliver M. Wrong
28. DISRUPTION OF MUSCLE STRESS-MEDIATED MINERAL ORIENTATION AT THE NANOSCALE IN THE SCAPULAR BONES OF RICKETS MICE WITH DEVELOPMENT
29. Disease Related Mutations Adjacent to Predicted Multiple Ca2+ Binding Sites of Ca2+-Sensing Receptor Altering Intracellular Ca2+ Oscillations via Extracellular Calcium and Amino Acid Signaling
30. Role of Multiple Endocrine Neoplasia Type 1 Mutational Analysis in Clinical Practice
31. A novel architecture for improving slew rate in FinFET-based op-amps and OTAs
32. Multiple endocrine neoplasia type 1 (MEN1)
33. Multiple endocrine neoplasia
34. Drain current model for nanoscale double-gate MOSFETs
35. Rickets and osteomalacia
36. Gastroenteropancreatic neuroendocrine tumours
37. Rickets and osteomalacia
38. X-linked hypoparathyroidism region on Xq27 is evolutionarily conserved with regions on 3q26 and 13q34 and contains a novel P-type ATPase
39. Characterization of GATA3 Mutations in the Hypoparathyroidism, Deafness, and Renal Dysplasia (HDR) Syndrome
40. Comparative ontogeny, processing, and segmental distribution of the renal chloride channel, ClC-5
41. Modeling study of human renal chloride channel (hCLC-5) mutations suggests a structural-functional relationship
42. Altered polarity and expression of H+-ATPase without ultrastructural changes in kidneys of Dent's disease patients
43. Fragmentation of filtered proteins and implications for glomerular protein sieving in Fanconi syndrome
44. Hypocalcaemic Disorders
45. Multiple Endocrine Neoplasia
46. Rickets and Osteomalacia
47. Glomerular protein sieving and implications for renal failure in Fanconi syndrome
48. Menin Interacts Directly with the Homeobox-Containing Protein Pem
49. MULTIPLE ENDOCRINE NEOPLASIA TYPE 1
50. Clinical and genetic studies of CLCN5 mutations in Japanese families with Dent's disease
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