R. Tammachote

发表

Ciliary and centrosomal defects associated with mutation and depletion of the Meckel syndrome genes MKS1 and MKS3.

V. Torres, P. Harris, V. Gattone, 2009, Human molecular genetics.

Triamcinolone acetonide alters expressions of matrix metalloproteinase-3 gene in primary human chondrocytes

N. Tammachote, R. Tammachote, M. Suntiparpluacha, 2016 .

Holocarboxylase synthetase deficiency: novel clinical and molecular findings

K. Suphapeetiporn, S. Tongkobpetch, S. Janklat, 2009, Clinical genetics.

The genetics behind osteoarthritis: Asian focus

R. Tammachote, 2011 .

Triamcinolone acetonide reduces viability, induces oxidative stress, and alters gene expressions of human chondrocytes.

N. Tammachote, R. Tammachote, M. Suntiparpluacha, 2016, European review for medical and pharmacological sciences.

Primary hyperoxaluria type 1 and brachydactyly mental retardation syndrome caused by a novel mutation in AGXT and a terminal deletion of chromosome 2

C. Srichomthong, K. Suphapeetiporn, V. Shotelersuk, 2012, American journal of medical genetics. Part A.

Phenolic Content and Biological Activities of Ethanol Extracts from Medicinal Plants in East Kalimantan, Indonesia

S. Prasongsuk, H. Punnapayak, W. Chavasiri, 2021, Sains Malaysiana.

A primary culture of mouse proximal tubular cells , established on collagen-coated membranes

Yanhong Wu, V. Torres, C. Ward, 2007 .

Identification and Functional Analysis of Six DAX1 Mutations in Patients With X-Linked Adrenal Hypoplasia Congenita

C. Srichomthong, K. Suphapeetiporn, V. Shotelersuk, 2018, Journal of the Endocrine Society.

Epitope-tagged Pkhd1 tracks the processing, secretion, and localization of fibrocystin.

J. V. van Deursen, Yanhong Wu, V. Torres, 2011, Journal of the American Society of Nephrology : JASN.

The Utilization of Karyotyping, iFISH, and MLPA for the Detection of Recurrence Genetic Aberrations in Multiple Myeloma

B. Rerkamnuaychoke, T. Chareonsirisuthigul, T. Siriboonpiputtana, 2017, Asian Pacific journal of cancer prevention : APJCP.

Characterization of PKD protein-positive exosome-like vesicles.

N. LaRusso, A. Leontovich, V. Torres, 2009, Journal of the American Society of Nephrology : JASN.

VDR and TNFSF11 polymorphisms are associated with osteoporosis in Thai patients.

A. Wongkularb, N. Tammachote, P. Yanatatsaneejit, 2018, Biomedical reports.

Effects of some psychiatric drugs on corticotropin-releasing factor (CRF) gene expression in mouse hypothalamus cells in vitro

V. Praphanphoj, R. Tammachote, M. Nantharat, 2016 .

Association study of the MMP1 gene polymorphism with knee osteoarthritis in Thais by high resolution melting (HRM) analysis

S. Honsawek, N. Tammachote, S. Kanitnate, 2013 .

Glucocorticoid receptor gene (NR3C1) promoter is hypermethylated in Thai females with major depressive disorder.

V. Praphanphoj, R. Tammachote, T. Wanitchanon, 2015, Genetics and molecular research : GMR.

Association between ADAM12 polymorphism and knee osteoarthritis in Thai population.

S. Honsawek, N. Tammachote, S. Kanitnate, 2016, The Knee.

ADAMTS14 gene polymorphism associated with knee osteoarthritis in Thai women.

S. Honsawek, N. Tammachote, S. Kanitnate, 2013, Genetics and molecular research : GMR.

A common and two novel GBA mutations in Thai patients with Gaucher disease

C. Srichomthong, K. Suphapeetiporn, V. Shotelersuk, 2013, Journal of Human Genetics.