검색결과 : 7건
| No. | Article |
|---|---|
| 1 |
Deciphering defective amelogenesis using in vitro culture systems Arinawati DY, Miyoshi K, Tanimura A, Horiguchi T, Hagita H, Noma T Journal of Bioscience and Bioengineering, 125(4), 479, 2018 |
| 2 |
Use of the MLPA Assay in the Molecular Diagnosis of Gene Copy Number Alterations in Human Genetic Diseases Stuppia L, Antonucci I, Palka G, Gatta V International Journal of Molecular Sciences, 13(3), 3245, 2012 |
| 3 |
In vitro receptor binding properties of a "painless" NGF mutein, linked to hereditary sensory autonomic neuropathy type V Covaceuszach S, Capsoni S, Marinelli S, Pavone F, Ceci M, Ugolini G, Vignone D, Amato G, Paoletti F, Lamba D, Cattaneo A Biochemical and Biophysical Research Communications, 391(1), 824, 2010 |
| 4 |
Clustering of disease-causing mutations on the domain-domain interfaces of ABCC6 Fulop K, Barna L, Symmons O, Zavodszky P, Varadi A Biochemical and Biophysical Research Communications, 379(3), 706, 2009 |
| 5 |
Alport Syndrome mutations in type IV tropocollagen alter molecular structure and nanomechanical properties Srinivasan M, Uzel SGM, Gautieri A, Keten S, Buehler MJ Journal of Structural Biology, 168(3), 503, 2009 |
| 6 |
Genomic organization, amplification, fine mapping, and intragenic polymorphisms of the human hemidesmosomal tetraspanin CD151 gene Whittock NV, McLean WHI Biochemical and Biophysical Research Communications, 281(2), 425, 2001 |
| 7 |
Etherphospholipid biosynthesis and dihydroxyactetone-phosphate acyltransferase: Resolution of the genomic organization of the human GNPAT gene and its use in the identification of novel mutations Ofman R, Lajmir S, Wanders RJA Biochemical and Biophysical Research Communications, 281(3), 754, 2001 |