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Your search keyword '"Amrathlal Rabbind Singh"' showing total 28 results

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28 results on '"Amrathlal Rabbind Singh"'

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1. Regulation of Streptomyces Chitinases by Two-Component Signal Transduction Systems and their Post Translational Modifications: A Review

9. Association of VEGFA promoter polymorphisms rs699947 and rs35569394 with diabetic retinopathy among North-Central Indian subjects: a case-control study

13. Signaling lymphocytic activation molecules Slam and cancers: friends or foes?

15. Growth hormone deficiency and pituitary malformation in a recurrent Cat-Eye syndrome: A family report

16. Gain‐of‐Function Mutation in STIM1 (P.R304W) Is Associated with Stormorken Syndrome

17. Phenotypic expression of a novel C282Y/R226G compound heterozygous state in HFE hemochromatosis: Molecular dynamics and biochemical studies

18. Human pre‐ <scp>B</scp> cell receptor signal transduction: evidence for distinct roles of <scp>PI</scp> 3 <scp>k</scp> inase and <scp>MAP</scp> ‐ <scp>k</scp> inase signalling pathways

19. RB/PLK1-dependent induced pathway by SLAMF3 expression inhibits mitosis and control hepatocarcinoma cell proliferation

20. A New Intergenic α -Globin Deletion ( α – α Δ125 ) Found in a Kabyle Population

21. Hepatocyte SLAMF3 reduced specifically the multidrugs resistance protein MRP-1 and increases HCC cells sensitization to anti-cancer drugs

22. Factors involved in CLL pathogenesis and cell survival are disrupted by differentiation of CLL B-cells into antibody-secreting cells

23. Stormorken syndrome or York platelet syndrome: A clinician's dilemma

24. Human pre-B cell receptor signal transduction: evidence for distinct roles of PI3kinase and MAP-kinase signalling pathways

25. ChiS histidine kinase negatively regulates the production of chitinase ChiC in Streptomyces peucetius

26. Gain-of-Function Mutation in STIM1 (P.R304W) Is Associated with Stormorken Syndrome

27. Identification of SLAMF3 (CD229) as an Inhibitor of Hepatocellular Carcinoma Cell Proliferation and Tumour Progression

28. Severe phenotypic spectrum of biallelic mutations in PRRT2 gene.

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