statistiche ricercatore

Nome	#
As little as needed: The extraordinary case of a mild recessive osteopetrosis owing to a novel splicing hypomorphic mutation in the TCIRG1 gene	3
A recessive contiguous gene deletion in chromosome16p13.3 leads to autosomal recessive osteopetrosis in a Jordanian patient.	2
A pre-screening FISH-based method to detect CRISPR/Cas9 off-targets in mouse embryonic stem cells	1
Fidelity of a YAC clone in the region of human MCF-2 gene	1
Chromosome Transplantation: Correction of the Chronic Granulomatous Disease Defect in Mouse Induced Pluripotent Stem Cells	1
Chloride channel ClCN7 mutations are responsible for severe recessive, dominant, and intermediate osteopetrosis	1
TCIRG1-dependent recessive osteopetrosis: mutation analysis, functional identification of the splicing defects, and in vitro rescue by U1 snRNA.	1
Human iPSC-based neurodevelopmental models of globoid cell leukodystrophy uncover patient- and cell type-specific disease phenotypes	1
Identification and purification of overlapping cosmid clones of the region Xq24-qter of human X chromosome using HPLC	1
SNX10 mutations define a subgroup of human autosomal recessive osteopetrosis with variable clinical severity.	1
Cell fusion is a physiological process in Mouse liver.	1
Totale	14

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2023/2024	10	0	0	0	0	0	0	0	0	1	1	7	1
2024/2025	4	2	2	0	0	0	0	0	0	0	0	0	0
Totale													14

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