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Bioinformation|October 12, 2023
Role of neutrophil-lymphocyte ratio as a prognostic marker for type 2 diabetic nephropathy among IndiansMurugan Subramani, Mudali Anbarasan, Deepalatha Shanmugam, et al.Journal of Bacteriology|August 4, 2009
Homologues of the Bacillus subtilis SpoVB protein are involved in cell wall metabolismPradeep Vasudevan, Jessica McElligott, Christa Attkisson, et al.Medrxiv : the Preprint Server for Health Sciences|September 16, 2024
Mutations in the U2 snRNA gene RNU2-2P cause a severe neurodevelopmental disorder with prominent epilepsyDaniel Greene, Koenraad De Wispelaere, Jon Lees, et al.Clinical Kidney Journal|April 9, 2015
Steroid-resistant nephrotic syndrome with mutations in NPHS2 (podocin): report from a three-generation familyVani Jain, John Feehally, Gabriela Jones, et al.American Journal of Medical Genetics. Part A|August 14, 2012
17q12 microdeletion syndrome: three patients illustrating the phenotypic spectrumAbhijit Dixit, Chirag Patel, Rachel Harrison, et al.Molecular Microbiology|August 24, 2007
Spore cortex formation in Bacillus subtilis is regulated by accumulation of peptidoglycan precursors under the control of sigma KPradeep Vasudevan, Amy Weaver, Erin D Reichert, et al.American Journal of Medical Genetics. Part A|June 10, 2024
Pathogenic FLNA variants affecting the hinge region of filamin A are associated with male survivalEmma M Wade, Tim Morgan, Gregory Gimenez, et al.American Journal of Human Genetics|October 22, 2019
Homozygous Loss-of-Function Mutations in AP1B1, Encoding Beta-1 Subunit of Adaptor-Related Protein Complex 1, Cause MEDNIK-like SyndromeHessa S Alsaif, Mohammad Al-Owain, Martin E Barrios-Llerena, et al.Endocrinology, Diabetes & Metabolism Case Reports|June 17, 2017
Intrauterine death following intraamniotic triiodothyronine and thyroxine therapy for fetal goitrous hypothyroidism associated with polyhydramnios and caused by a thyroglobulin mutationPradeep Vasudevan, Corrina Powell, Adeline K Nicholas, et al.Neurology|July 13, 2018
Retinal and optic nerve changes in microcephaly: An optical coherence tomography studyEleni Papageorgiou, Anastasia Pilat, Frank Proudlock, et al.Pageof 16