Works matching IS 00221333 AND DT 2023 AND VI 102 AND IP 1
Results: 30
Prevalence of congenital sucrase-isomaltase deficiency in Turkey may be much higher than the estimates.
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- Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-023-01428-8
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Role of cryptic rearrangements of human chromosomes in the aetiology of schizophrenia.
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- Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-023-01427-9
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Dual effect of methylene-tetrahydrofolate reductase and angiotensin-converting enzyme gene polymorphisms on the risk of acute ischemic stroke.
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- Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-023-01425-x
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Identification of fertility restorers for A<sub>2</sub> cytoplasm-based CGMS lines and development of short duration hybrids in pigeonpea (Cajanus cajan (L.) Millsp.)
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- Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-023-01426-w
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Association of ABCA1 R219K polymorphism and telomere length in a Chinese rural population: possible linking to systemic inflammation.
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- Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-023-01424-y
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Distinct gene expression patterns of SOX2 and SOX2OT variants in different types of brain tumours.
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- Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-023-01423-z
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Mitochondrial markers differentiate two distinct phylogenetic groups in indigenous rice landraces of northeast India: an evolutionary insight.
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- Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-023-01422-0
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Differential expression of the androgen receptor gene is correlated with CAG polymorphic repeats in patients with prostate cancer.
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- Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-023-01421-1
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Intronic OTOF mutation causes an atypical splicing defect resulting in auditory neuropathy spectrum disorder.
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- Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-023-01420-2
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Transcribed intergenic regions exhibit a lower frequency of nucleotide polymorphism than the untranscribed intergenic regions in the genomes of Escherichia coli and Salmonella enterica.
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- Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-023-01418-w
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Identification of genetic polymorphism of the MBL2 gene and its association with clinical mastitis in Murrah buffaloes.
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- Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-023-01419-9
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First detection of endopolyploidy in tapetal cells and chromosomal anomalies in meiocytes of Viola pilosa cytotypes (2n=20) from Pir Panjal (Himalayas)
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- Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-022-01415-5
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Identification of a novel mutation in the HACD1 gene in an Iranian family with autosomal recessive congenital myopathy, with fibre-type disproportion.
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- Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-022-01417-3
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Individuals with T-786C and G894T genotypes of eNOS in Chinese Han population have an increased risk of developing rheumatoid arthritis.
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- Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-022-01400-y
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Imputation of SNPs associated with presbycusis through linkage disequilibrium analysis in the ILDR1 gene.
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- Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-022-01416-4
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Celiac disease-associated loci show considerable genetic overlap with neuropsychiatric diseases but with limited transethnic applicability.
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- Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-022-01413-7
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A novel variant of TNNC1 associated with severe dilated cardiomyopathy causing infant mortality and stillbirth: a case of germline mosaicism.
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- Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-022-01412-8
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EMX2OS targeting IGF2BP1 represses Wilms' tumour stemness, epithelial–mesenchymal transition and metastasis.
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- Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-022-01411-9
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Is the fundamental pathology in Duchenne's muscular dystrophy caused by a failure of glycogenolysis–glycolysis in costameres?
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- Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-022-01410-w
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Exome sequencing and microarray identified a novel large exonic deletion in SYT2 gene in an ultra-rare case with recessive CMS type 7.
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- Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-022-01409-3
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CRISPR-Cas9 F0 knockout approach using predesigned in vitro transcribed guide RNAs partially recapitulates Rx3 function in eye morphogenesis.
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- Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-022-01408-4
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Population genetic structure and evolutionary demographic patterns of Phrynoderma karaavali, an edible frog species of Kerala, India.
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- Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-022-01407-5
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Diagnosis of prenatal 22q11.2 duplication syndrome: a two-case study.
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- Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-022-01406-6
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A time-calibrated mitogenomic phylogeny suggests that Korean Hyalessa fuscata is a bridge between Chinese and Japanese H. maculaticollis.
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- Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-022-01405-7
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Relationship between leptin gene variants (–2548G>A and 19A>G) and obesity among north Indian Punjabi population.
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- Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-022-01401-x
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Arginase deficiency in Bulgaria: first cases and potential endemic region for the disorder.
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- Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-022-01399-2
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Remnants of SIRE1 retrotransposons in human genome?
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- Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-022-01398-3
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LncRNA TTN-AS1 exacerbates extracellular matrix accumulation via miR-493-3p/FOXP2 axis in diabetic nephropathy.
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- Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-022-01397-4
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Panmictic stock structure of milkfish (Chanos chanos, Forsskål 1775) from Indian waters determined using mtDNA marker.
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- Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-022-01395-6
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Mysteries in our genome.
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- Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-022-01392-9
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