Associated Papers
Dual phenotypes in recurrent astrocytoma, IDH-mutant; coexistence of IDH-mutant and IDH-wildtype components: a case report with genetic and epigenetic analysis.
Yamaguchi J et al.
Acta Neuropathologica Communications, 2024
39456052 (PubMed )
Supplement: 40478_2024_1879_MOESM3_ESM.xlsx › NGY-P
The association between TNP2 gene polymorphisms and Iranian infertile men with varicocele: A case-control study.
Heidari MM et al.
International Journal of Reproductive Biomedicine, 2019
Actionable perturbations of damage responses by TCL1/ATM and epigenetic lesions form the basis of T-PLL.
Schrader A et al.
Nature Communications, 2018
29449575 (PubMed )
Supplement: 41467_2017_2688_MOESM20_ESM.xlsx › e__Freq_TP095
A G613A missense in the Hutchinson's progeria lamin A/C gene causes a lone, autosomal dominant atrioventricular block.
Villa F et al.
Immunity & Ageing : I & A, 2014
25469153 (PubMed )
Supplement: 12979_2014_19_MOESM2_ESM.xls › Sheet1
Association study of six SNPs in PRM1, PRM2 and TNP2 genes in iranian infertile men with idiopathic azoospermia.
Siasi E et al.
Iranian Journal of Reproductive Medicine, 2012
Analysis of sperm nuclear protein gene polymorphisms and DNA integrity in infertile men.
Venkatesh S et al.
Systems Biology in Reproductive Medicine, 2011
Mutations in the protamine locus: association with spermatogenic failure?
Imken L et al.
Molecular Human Reproduction, 2009
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