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Cloning, expression and chromosomal localization of a human testis 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase geneHMG20A and HMG20B map to human chromosomes 15q24 and 19p13.3 and constitute a distinct class of HMG-box genes with ubiquitous expressionRole of UEV-1, an inactive variant of the E2 ubiquitin-conjugating enzymes, in in vitro differentiation and cell cycle behavior of HT-29-M6 intestinal mucosecretory cells.Molecular cloning, expression, and chromosomal localization of a ubiquitously expressed human 6-phosphofructo-2-kinase/ fructose-2, 6-bisphosphatase gene (PFKFB3)Minibrain (MNBH) is a single copy gene mapping to human chromosome 21q22.2Hepatitis A virus receptor blocks cell differentiation and is overexpressed in clear cell renal cell carcinomaIdentification of somatic and germline mitochondrial DNA sequence variants in prostate cancer patientsAssignment of the gene responsible for cystinuria (rBAT) and of markers D2S119 and D2S177 to 2p16 by fluorescence in situ hybridizationAdditional complexity on human chromosome 15q: identification of a set of newly recognized duplicons (LCR15) on 15q11-q13, 15q24, and 15q26.Human chromosome 15q11-q14 regions of rearrangements contain clusters of LCR15 duplicons.Dscr1, a novel endogenous inhibitor of calcineurin signaling, is expressed in the primitive ventricle of the heart and during neurogenesis.Cloning of the human phospholipase A2 activating protein (hPLAP) gene on the chromosome 9p21 melanoma deleted region.The human HERC3 gene maps to chromosome 4q21 by fluorescence in situ hybridization.The human intersectin genes and their spliced variants are differentially expressed.Fetal liver-derived mesenchymal stem cell engraftment after allogeneic in utero transplantation into rabbitsHigh-titer retroviral vectors containing the enhanced green fluorescent protein gene for efficient expression in hematopoietic cells.Comparative genomic hybridization analysis reveals new different subgroups in early-stage bladder tumors.The β-interferon scaffold attachment region confers high-level transgene expression and avoids extinction by epigenetic modifications of integrated provirus in adipose tissue-derived human mesenchymal stem cells.Altered expression of 12S/MT-RNR1, MT-CO2/COX2, and MT-ATP6 mitochondrial genes in prostate cancer.A patient with autistic disorder and a 20/22 chromosomal translocation.Molecular characterization of a t(9;12)(p21;q13) balanced chromosome translocation in combination with integrative genomics analysis identifies C9orf14 as a candidate tumor-suppressor.Aneuploidy of chromosome Y in prostate tumors and seminal vesicles: a possible sign of aging rather than an indicator of carcinogenesis?Stromal interaction molecule 2 (STIM2) is frequently overexpressed in colorectal tumors and confers a tumor cell growth suppressor phenotype.Suitability of oligonucleotide-mediated cystic fibrosis gene repair in airway epithelial cellsA Polymorphic Genomic Duplication on Human Chromosome 15 Is a Susceptibility Factor for Panic and Phobic DisordersMitotic recombination effects homozygosity for NF1 germline mutations in neurofibromasPaternal origin of a de novo novel CFTR mutation (L1065R) causing cystic fibrosisComprehensive molecular characterisation of hereditary non-polyposis colorectal tumours with mismatch repair proficiency[Bourneville's tuberous sclerosis associated with double uterus and vagina (didelphic uterus)]Tissue imprints or primary cultures: which strategy to use to study cytogenetic clonality?
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P50
description
researcher ORCID ID = 0000-0002-5739-1693
@en
wetenschapper
@nl
name
Marga Nadal
@ast
Marga Nadal
@en
Marga Nadal
@es
Marga Nadal
@nl
type
label
Marga Nadal
@ast
Marga Nadal
@en
Marga Nadal
@es
Marga Nadal
@nl
prefLabel
Marga Nadal
@ast
Marga Nadal
@en
Marga Nadal
@es
Marga Nadal
@nl
P106
P21
P31
P496
0000-0002-5739-1693