Suchergebnisse - "Srivastava, Priyanka"

PubPharm (283)

51

Gas Chromatography Mass Spectrometry Aided Diagnosis of Glutathione Synthetase Deficiency

enthalten in: Laboratory medicine | 2022

von Kaur, P. | Chaudhry, C. | Panigrahi, I. | +2

52

Genotype-phenotype spectrum of 130 unrelated Indian families with Mucopolysaccharidosis type II

enthalten in: European journal of medical genetics | 2022

von Agrawal, N. | Verma, G. | Saxena, D. | +17

53

A novel c.1937T>C (p.Leu646Pro) missense mutation in a patient with Leber congenital amaurosis

enthalten in: Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus | 2022

von Kaur, S. | Sukhija, J. | Kaur, A. | +4

54

Bacillus subtilis Histidine Kinase KinC Activates Biofilm Formation by Controlling Heterogeneity of Single-Cell Responses

enthalten in: mBio | 2022

von Chen, Z. | Srivastava, P. | Zarazúa-Osorio, B. | +3

55

Skeletal muscle myosin promotes coagulation by binding factor XI via its A3 domain and enhancing thrombin-induced factor XI activation

enthalten in: The Journal of biological chemistry | 2022

von Morla, S. | Deguchi, H. | Zilberman-Rudenko, J. | +5

56

Role of miRNA polymorphism in recurrent pregnancy loss : a systematic review and meta-analysis

enthalten in: Biomarkers in medicine | 2022

von Srivastava, P. | Bamba, C. | Chopra, S. | +1

57

Molecular analysis of severe hemophilia B in Indian families : Identification of mutational hotspot and novel variants

enthalten in: International journal of laboratory hematology | 2022

von Agrawal, N. | Kumar, R. | Masih, S. | +7

58

Exploration of Potential Biomarker Genes and Pathways in Kawasaki Disease : An Integrated in-Silico Approach

enthalten in: Frontiers in genetics | 2022

von Srivastava, P. | Bamba, C. | Pilania, R. | +4

59

Self-Reported Depression Is Associated With Aberration in Emotional Reactivity and Emotional Concept Coding

enthalten in: Frontiers in psychology | 2022

von Sheoran, H. | Srivastava, P.

60

Whole-exome sequencing and variant spectrum in children with suspected inherited renal tubular disorder: the East India Tubulopathy Gene Study

enthalten in: Pediatric nephrology | 2022

von Sinha, R. | Pradhan, S. | Banerjee, S. | +13