A large number of cerebral microbleeds in CADASIL patients presenting with recurrent seizures: a case report by Chumpol Anamnart, Dittapong Songsaeng, Sirisak Chanprasert

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Effect of seed priming with different concentrations of potassium nitrate on the pattern of seed imbibition and germination of rice (Oryza sativa L.) by Anisa Ruttanaruangboworn, Wanchai Chanprasert, Pitipong Tobunluepop, Damrongvudhi Onwimol

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Flavonoid component determination and apoptotic induction evaluation of houttuynia cordata thunb extract on human acute leukemic cells by Boonyawee N, Chaowanee W, Paweena P, Supantitra Chanprasert

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Optimization and sensitivity analysis of fast ethanol assay in maize seeds by Damrongvudhi Onwimol, Thunyapuk Rongsangchaicharean, Pitipong Thobunluepop, Tanapon Chaisan, Wanchai Chanprasert

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Affordable Technology for Enumeration of the Absolute CD4 T-Lymphocyte Count by Cell Bead Assay by Nantakomol, D, Chanprasert, S, Soogarun, S, Imwong, M, Ohashi, J, Nuchnoi, P

WASP: a Web-based Allele-Specific PCR assay designing tool for detecting SNPs and mutations by Assawamakin Anunchai, Chanprasert Juntima, Ruangrit Uttapong, Ngamphiw Chumpol, Chaichoompu Kridsadakorn, Wangkumhang Pongsakorn, Tongsima Sissades

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Generation of an induced pluripotent stem cell line (MUSIi015-A) from a diabetic patient carrying mutations in ZYG11A (p.L475P) and GATA6 (p.E51K) by Siriwal Suwanpitak, Chutima Chanprasert, Ratchapong Netsrithong, Nattachet Plengvidhya, Pa-thai Yenchitsommanus, Methichit Wattanapanitch, Prapaporn Jungtrakoon Thamtarana

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Study on the effect of green pit viper venom (Trimeresurus albolabris) on platelet morphology by flow cytometry by Suphan Soogarun, Montri Choewbamrungkiat, Viroj Wiwanitkit, Jamsai Suwansaksri, Waykin Nopanitaya, Paweena Pradniwat, Attakorn Palasuwan, Supantitra Chanprasert

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Telepharmacy during home isolation: drug-related problems and pharmaceutical care in COVID-19 patients receiving antiviral therapy in Thailand by Worapong Sungsana, Chotirat Nakaranurack, Benjabhorn Weeraphon, Watsa Charoenwaiyachet, Supparat Chanprasert, Pattama Torvorapanit, Wichai Santimaleeworagun, Opass Putcharoen

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Generation of an induced pluripotent stem cell line (MUSIi014-A) from an affected member of a family with autosomal dominant diabetes carrying p.L475P mutation in ZYG11A gene assoc... by Chutima Chanprasert, Nutchanawan Promnakhon, Nontaphat Thongsin, Siriwal Suwanpitak, Nattachet Plengvidhya, Pa-thai Yenchitsommanus, Prapaporn Jungtrakoon Thamtarana, Methichit Wattanapanitch

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Characterization of microsatellites and gene contents from genome shotgun sequences of mungbean (<it>Vigna radiata </it>(L.) Wilczek) by Sommanas Warunee, Seehalak Worapa, Sangsrakru Duangjai, Chanprasert Juntima, Uthaipaisanwong Pichahpuk, Somta Prakit, Tangphatsornruang Sithichoke, Tragoonrung Somvong, Srinives Peerasak

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Novel adiponectin variants identified in type 2 diabetic patients reveal multimerization and secretion defects. by Prapaporn Jungtrakoon, Nattachet Plengvidhya, Watip Tangjittipokin, Sarin Chimnaronk, Wanisa Salaemae, Nalinee Chongjaroen, Kanjana Chanprasert, Jatuporn Sujjitjoon, Chatchawan Srisawat, Pa-Thai Yenchitsomanus

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An induced pluripotent stem cell line (MUSIi019-A) generated from a patient with distal renal tubular acidosis carrying a compound heterozygous mutation in solute carrier family 4... by Narissara Kaewboonlert, Methichit Wattanapanitch, Oranud Praditsap, Nipaporn Deejai, Chutima Chanprasert, Nunghathai Sawasdee, Choochai Nettuwakul, Wanchai Wanachiwanawin, Suchai Sritippayawan, Prapaporn Jungtrakoon Thamtarana, Pa-thai Yenchitsomanus, Nanyawan Rungroj

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P099: Mosaic variant in RHOA in an adolescent with a multisystem disorder composed of congenital and progressive anomalies by Aimee Allworth, Ian Glass, Anne Hing, Elizabeth Blue, Elisabeth Rosenthal, Sam Strohbehn, Gail Jarvik, Katrina Dipple, Andrew Stergachis, Virginia Sybert, Jane Ranchalis, Martha Horike-Pyne, Sirisak Chanprasert, Fuki Hisama, Michael Bamshad, James Bennett, Heather Brandling-Bennett, Michelle Cabrera, Mark Wener

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Dominant‐negative variant in SLC1A4 causes an autosomal dominant epilepsy syndrome by Jonai Pujol‐Giménez, Ghayda Mirzaa, Elizabeth E. Blue, Giuseppe Albano, Danny E. Miller, Aimee Allworth, James T. Bennett, Peter H. Byers, Sirisak Chanprasert, Jingheng Chen, Daniel Doherty, Andrew B. Folta, Madelyn A. Gillentine, Ian Glass, Anne Hing, Martha Horike‐Pyne, Kathleen A. Leppig, Azma Parhin, Jane Ranchalis, Wendy H. Raskind, Elisabeth A. Rosenthal, Ulrike Schwarze, Sam Sheppeard, Samuel Strohbehn, Virginia P. Sybert, Andrew Timms, Mark Wener, University of Washington Center for Mendelian Genomics (UW‐CMG)a, Undiagnosed Diseases Network (UDN), Michael J. Bamshad, Fuki M. Hisama, Gail P. Jarvik, Katrina M. Dipple, Matthias A. Hediger, Andrew B. Stergachis

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