Page last updated: 2024-09-05

biotin and Cystinuria

biotin has been researched along with Cystinuria in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Creemers, JW; de Zegher, F; Derua, R; Eyskens, F; Francois, I; Jaeken, J; Lecointre, C; Martens, K; Matthijs, G; Meulemans, S; Slootstra, JW; Waelkens, E	1

Other Studies

1 other study(ies) available for biotin and Cystinuria

Article	Year
Deletion of PREPL, a gene encoding a putative serine oligopeptidase, in patients with hypotonia-cystinuria syndrome. American journal of human genetics, 2006, Volume: 78, Issue:1 Topics: Amino Acid Sequence; Amino Acid Transport Systems, Basic; Amino Acid Transport Systems, Neutral; Base Sequence; Biotin; Blotting, Northern; Chromosomes, Human, Pair 2; Cystinuria; Electrophoresis, Polyacrylamide Gel; Gene Deletion; Genes, Recessive; Humans; Immunohistochemistry; Infant; Infant, Newborn; Molecular Sequence Data; Muscle Hypotonia; Mutagenesis, Site-Directed; Organophosphorus Compounds; Prolyl Oligopeptidases; Reverse Transcriptase Polymerase Chain Reaction; Sequence Analysis, DNA; Serine Endopeptidases; Substrate Specificity; Syndrome	2006

Article

Year

Deletion of PREPL, a gene encoding a putative serine oligopeptidase, in patients with hypotonia-cystinuria syndrome.

American journal of human genetics, 2006, Volume: 78, Issue:1

Topics: Amino Acid Sequence; Amino Acid Transport Systems, Basic; Amino Acid Transport Systems, Neutral; Base Sequence; Biotin; Blotting, Northern; Chromosomes, Human, Pair 2; Cystinuria; Electrophoresis, Polyacrylamide Gel; Gene Deletion; Genes, Recessive; Humans; Immunohistochemistry; Infant; Infant, Newborn; Molecular Sequence Data; Muscle Hypotonia; Mutagenesis, Site-Directed; Organophosphorus Compounds; Prolyl Oligopeptidases; Reverse Transcriptase Polymerase Chain Reaction; Sequence Analysis, DNA; Serine Endopeptidases; Substrate Specificity; Syndrome

2006