about
The antimicrobial compound xantholysin defines a new group of Pseudomonas cyclic lipopeptidesDraft Genome Sequence of Kocuria rhizophila RF, a Radiation-Resistant Soil IsolateNovel Mutation of ZAP-70-related Combined Immunodeficiency: First Case from the National Iranian Registry and Review of the Literature.Co-expressional conservation in virulence and stress related genes of three Gammaproteobacterial species: Escherichia coli, Salmonella enterica and Pseudomonas aeruginosa.Functional Evaluation of an IKBKG Variant Suspected to Cause Immunodeficiency Without Ectodermal Dysplasia.Genetic and functional characterization of cyclic lipopeptide white-line-inducing principle (WLIP) production by rice rhizosphere isolate Pseudomonas putida RW10S2.Draft Genome Sequence of Pseudomonas fluorescens LMG 5329, a White Line-Inducing Principle-Producing Bioindicator for the Mushroom Pathogen Pseudomonas tolaasiiDistinct lipopeptide production systems for WLIP (white line-inducing principle) in Pseudomonas fluorescens and Pseudomonas putida.Impact of a stereocentre inversion in cyclic lipodepsipeptides from the viscosin group: a comparative study of the viscosinamide and pseudodesmin conformation and self-assembly.PCR detection of novel non-ribosomal peptide synthetase genes in lipopeptide-producing Pseudomonas.Draft Genome Sequence of Pseudomonas gingeri Strain LMG 5327, the Causative Agent of Ginger Blotch in Agaricus bisporus.Assessing the impact of exact reads on reducing the error rate of read mappingDraft Genome Sequence of Pseudomonas aeruginosa Strain LMG 1272, an Atypical White Line Reaction ProducerA novel homozygous LRRK1 stop gain mutation in a patient suspected with osteosclerotic metaphyseal dysplasiaWhole exome sequencing identifies both nuclear and mitochondrial variations in an Iranian family with non-syndromic hearing lossInherited IFNAR1 deficiency in otherwise healthy patients with adverse reaction to measles and yellow fever live vaccinesMosaic trisomy 22 in a 4-year-old boy with congenital heart disease and general hypotrophy: A case reportAuto-inflammation in a Patient with a Novel Homozygous OTULIN MutationGATA4 screening in Iranian patients of various ethnicities affected with congenital heart disease: Co-occurrence of a novel de novo translocation (5;7) and a likely pathogenic heterozygous GATA4 mutation in a family with autosomal dominant congenita
P50
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P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Hassan Rokni-Zadeh
@ast
Hassan Rokni-Zadeh
@en
Hassan Rokni-Zadeh
@es
Hassan Rokni-Zadeh
@nl
Hassan Rokni-Zadeh
@sl
type
label
Hassan Rokni-Zadeh
@ast
Hassan Rokni-Zadeh
@en
Hassan Rokni-Zadeh
@es
Hassan Rokni-Zadeh
@nl
Hassan Rokni-Zadeh
@sl
prefLabel
Hassan Rokni-Zadeh
@ast
Hassan Rokni-Zadeh
@en
Hassan Rokni-Zadeh
@es
Hassan Rokni-Zadeh
@nl
Hassan Rokni-Zadeh
@sl
P1053
B-8098-2008
P106
P1153
23475096200
P21
P31
P3829
P496
0000-0001-5503-0344