statistiche ricercatore

Nome	#
Molecular insight into the synergism between the minor allele of human liver peroxisomal alanine: Glyoxylate aminotransferase and the F152I mutation	100
Human liver peroxisomal alanine:glyoxylate aminotransferase: Different stability under chemical stress of the major allele, the minor allele, and its pathogenic G170R variant.	98
Biochemical analyses are instrumental in identifying the impact of mutations on holo and/or apo-forms and on the region(s) of alanine:glyoxylate aminotransferase variants associated with Primary Hyperoxaluria Type I.	97
Molecular defects of the glycine 41 variants of alanine glyoxylate aminotransferase associated with primary hyperoxaluria type I	92
Molecular insight into the synergism between the minor allele of human liver peroxisomal alanine: glyoxylate aminotransferase and the f152i mutation	87
The Chaperoning Activity of Amino-oxyacetic Acid on Folding-Defective Variants of Human Alanine:Glyoxylate Aminotransferase Causing Primary Hyperoxaluria Type I	85
SHEDDING LIGHT ON THE MOLECULAR DEFECT OF TWOALANINE:GLYOXYLATE AMINOTRANSFERASE PATHOGENIC VARIANTS:A BIOCHEMICAL APPROACH.	83
Totale	642

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2019/2020	45	0	0	0	0	0	0	8	6	4	9	1	17
2020/2021	75	16	15	3	10	11	4	2	5	5	0	3	1
2021/2022	91	8	29	16	5	3	4	2	5	5	0	3	11
2022/2023	123	7	13	15	16	11	35	2	4	14	1	3	2
2023/2024	64	4	2	4	11	3	7	0	9	2	6	11	5
2024/2025	63	7	7	3	29	9	8	0	0	0	0	0	0
Totale													642

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