Lin KL

References (3)

Title : Severe neonatal MEGDHEL syndrome with a homozygous truncating mutation in SERAC1 - Fellman_2022_Biochim.Biophys.Acta.Mol.Basis.Dis_1868_166298
Author(s) : Fellman V , Banerjee R , Lin KL , Pulli I , Cooper H , Tyynismaa H , Kallijarvi J
Ref : Biochimica & Biophysica Acta Mol Basis Dis , 1868 :166298 , 2022
Abstract :
PubMedSearch : Fellman_2022_Biochim.Biophys.Acta.Mol.Basis.Dis_1868_166298
PubMedID: 34751152
Gene_locus related to this paper: human-SERAC1

Title : Effect of CYP2D6 and CYP3A4 Genotypes on the Efficacy of Cholinesterase Inhibitors in Southern Chinese Patients With Alzheimer's Disease - Ma_2019_Am.J.Alzheimers.Dis.Other.Demen__1533317519848237
Author(s) : Ma SL , Tang NLS , Wat KHY , Tang JHY , Lau KH , Law CB , Chiu J , Tam CCW , Poon TK , Lin KL , Kng CPL , Kong HL , Chan TY , Chan WC , Lam LCW
Ref : Am J Alzheimers Dis Other Demen , :1533317519848237 , 2019
Abstract :
PubMedSearch : Ma_2019_Am.J.Alzheimers.Dis.Other.Demen__1533317519848237
PubMedID: 31064198

Title : Docking study of the precursor peptide of mastoparan onto its putative processing enzyme, dipeptidyl peptidase IV: a revisit to molecular ticketing - Jang_2010_J.Comput.Aided.Mol.Des_24_213
Author(s) : Jang S , Chung TY , Shin J , Lin KL , Tzen JT , Li FY
Ref : J Comput Aided Mol Des , 24 :213 , 2010
Abstract :
PubMedSearch : Jang_2010_J.Comput.Aided.Mol.Des_24_213
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