N. Rungroj

发表

A Novel Missense Mutation in AE1 Causing Autosomal Dominant Distal Renal Tubular Acidosis Retains Normal Transport Function but Is Mistargeted in Polarized Epithelial Cells*

F. Reimann, W. Bennett, M. Devonald, 2004, Journal of Biological Chemistry.

A novel splice‐acceptor site mutation (IVS13‐2A>T) of polycystic kidney disease 1 (PKD1) gene resulting in an RNA processing defect with a 74‐nucleotide deletion in exon 14 of the mRNA transcript

P. Wilairat, P. Yenchitsomanus, N. Rungroj, 2000, Human mutation.

Use of reverse transcription-polymerase chain reaction for cloning of coat protein-encoding genes of cymbidium mosaic virus.

P. Srifah, S. Loprasert, S Loprasert, 1996, Gene.

Identification of the Conserved Sequences at the Species Level of Odontoglossum Ringspot Virus and Other Members of Tobamovirus by Its Coat Protein Sequence Analysis

P. Srifah, N. Rungroj, 2006 .

Molecular mechanisms of autosomal dominant and recessive distal renal tubular acidosis caused by SLC4A1 (AE1) mutations

R. Reithmeier, S. Kittanakom, P. Yenchitsomanus, 2005, Journal of molecular and genetic medicine : an international journal of biomedical research.

Association between Human Prothrombin Variant (T165M) and Kidney Stone Disease

P. Yenchitsomanus, Prapaporn Jungtrakoon, N. Rungroj, 2012, PloS one.

Prothrombin haplotype associated with kidney stone disease in Northeastern Thai patients.

P. Yenchitsomanus, V. Akkarapatumwong, P. Malasit, 2011, Urology.

Impaired trafficking and instability of mutant kidney anion exchanger 1 proteins associated with autosomal recessive distal renal tubular acidosis

N. Deejai, P. Yenchitsomanus, N. Rungroj, 2022, BMC Medical Genomics.

Molecular Genetics of Kidney Stone Disease

P. Yenchitsomanus, N. Rungroj, N. Sawasdee, 2014 .

Association between intelectin-1 variation and human kidney stone disease in northeastern Thai population

P. Yenchitsomanus, N. Rungroj, S. Sritippayawan, 2021, Urolithiasis.

Correlation between genotypes of F2 rs5896 (p.Thr165Met) polymorphism and urinary prothrombin fragment 1

P. Yenchitsomanus, N. Rungroj, S. Sritippayawan, 2018, Urolithiasis.

A novel loss-of-function mutation of PBK associated with human kidney stone disease

N. Deejai, W. Chaowagul, P. Yenchitsomanus, 2020, Scientific Reports.

Distal renal tubular acidosis caused by tryptophan‐aspartate repeat domain 72 (WDR72) mutations

N. Deejai, P. Yenchitsomanus, S. Khositseth, 2018, Clinical genetics.

Loss-of-function mutations of SCN10A encoding NaV1.8 α subunit of voltage-gated sodium channel in patients with human kidney stone disease

S. Dib-Hajj, S. Waxman, W. Chaowagul, 2018, Scientific Reports.

Simple, efficient, and cost-effective multiplex genotyping with matrix assisted laser desorption/ionization time-of-flight mass spectrometry of hemoglobin beta gene mutations.

P. Wilairat, P. Yenchitsomanus, S. Yongkiettrakul, 2009, The Journal of molecular diagnostics : JMD.

Molecular Diagnosis of Solute Carrier Family 4 Member 1 (SLC4A1) Mutation–Related Autosomal Recessive Distal Renal Tubular Acidosis

N. Deejai, P. Yenchitsomanus, S. Khositseth, 2018, Laboratory medicine.

A whole genome SNP genotyping by DNA microarray and candidate gene association study for kidney stone disease

P. Yenchitsomanus, N. Rungroj, S. Sritippayawan, 2014, BMC Medical Genetics.

ด้วยวิธี high resolution melting Analysis of SCN 10 A Gene Mutation in Northeastern Thai Patients with Nephrolithiasis by High Resolution Melting Method

P. Yenchitsomanus, N. Rungroj, N. Sawasdee, 2013 .

Novel ATP6V1B1 and ATP6V0A4 mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing loss

S. Bianca, C. Morton, V. Tasic, 2002, Journal of medical genetics.

Novel ATP 6 V 1 B 1 and ATP 6 V 0 A 4 mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing loss

S. Bianca, C. Morton, V. Tasic, 2002 .

Novel and de novo PKD1 mutations identified by multiple restriction fragment-single strand conformation polymorphism (MRF-SSCP)

P. Yenchitsomanus, C. Limwongse, W. Thongnoppakhun, 2004, BMC Medical Genetics.

Trafficking defect of mutant kidney anion exchanger 1 (kAE1) proteins associated with distal renal tubular acidosis and Southeast Asian ovalocytosis.

P. Yenchitsomanus, V. Akkarapatumwong, Wandee Udomchaiprasertkul, 2006, Biochemical and biophysical research communications.

Evidence suggesting a genetic contribution to kidney stone in northeastern Thai population

P. Yenchitsomanus, P. Malasit, S. Nakjang, 2009, Urological Research.