Lin WD - Search Results

1

A pilot study of neonatal screening by electrospray ionization tandem mass spectrometry in Taiwan.

Lin WD, Wu JY, Lai CC, Tsai FJ, Tsai CH, Lin SP, Niu DM. Lin WD, et al. Among authors: lin sp. Acta Paediatr Taiwan. 2001 Jul-Aug;42(4):224-30. Acta Paediatr Taiwan. 2001. PMID: 11550411

2

Rapid monitoring assay of congenital adrenal hyperplasia with microbore high-performance liquid chromatography/electrospray ionization tandem mass spectrometry from dried blood spots.

Lai CC, Tsai CH, Tsai FJ, Lee CC, Lin WD. Lai CC, et al. Among authors: lin wd. Rapid Commun Mass Spectrom. 2001;15(22):2145-51. doi: 10.1002/rcm.493. Rapid Commun Mass Spectrom. 2001. PMID: 11746879

3

Pitfalls of PCR-based genotyping in patients with 21-hydroxylase deficiency.

Tsai CH, Lin WD, Tsai FJ, Peng CT, Wu JY. Tsai CH, et al. Among authors: lin wd. Acta Paediatr Taiwan. 2001 May-Jun;42(3):145-50. Acta Paediatr Taiwan. 2001. PMID: 11431859

4

Mutation analysis of a family with hereditary hemorrhagic telangiectasia associated with hepatic arteriovenous malformation.

Lin WD, Wu JY, Hsu HB, Tsai FJ, Lee CC, Tsai CH. Lin WD, et al. J Formos Med Assoc. 2001 Dec;100(12):817-9. J Formos Med Assoc. 2001. PMID: 11802521

5

Identification of a polymorphism (D366H) in the endoglin gene in Chinese.

Lin WD, Tsai FJ, Lee CC, Wu JY. Lin WD, et al. Hum Mutat. 2000 Jun;15(6):583. doi: 10.1002/1098-1004(200006)15:6<583::AID-HUMU23>3.0.CO;2-#. Hum Mutat. 2000. PMID: 10862100 No abstract available.

6

Identification of a polymorphism (G83S) in the TWIST gene in Taiwanese.

Yang CF, Wu JY, Tsai FJ, Lee CC, Lin WD. Yang CF, et al. Among authors: lin wd. Hum Mutat. 2000 Nov;16(5):448. doi: 10.1002/1098-1004(200011)16:5<448::AID-HUMU21>3.0.CO;2-#. Hum Mutat. 2000. PMID: 11058914 No abstract available.

7

A stop codon mutation in the CBFA 1 gene causes cleidocranial dysplasia.

Tsai FJ, Wu JY, Lin WD, Tsai CH. Tsai FJ, et al. Among authors: lin wd. Acta Paediatr. 2000 Oct;89(10):1262-5. doi: 10.1080/080352500750027673. Acta Paediatr. 2000. PMID: 11083386 No abstract available.

8

Identification of a polymorphism (D168N) in the XRP2 gene in Chinese.

Lin WD, Shi YR, Tsai FJ, Lee CC, Lin HJ, Wu JY. Lin WD, et al. Among authors: lin hj. Hum Mutat. 2001 Apr;17(4):354. doi: 10.1002/humu.43. Hum Mutat. 2001. PMID: 11295842 No abstract available.

9

The involvement of insulin receptor genotypes in pre- and co-obese acanthosis Nigricans children and adolescent.

Wang CH, Lin WD, Bau DT, Chou IC, Tsai CH, Tsai FJ. Wang CH, et al. Among authors: lin wd. J Pediatr Endocrinol Metab. 2010 Jul;23(7):653-60. J Pediatr Endocrinol Metab. 2010. PMID: 20857837

10

PTPRD silencing by DNA hypermethylation decreases insulin receptor signaling and leads to type 2 diabetes.

Chen YT, Lin WD, Liao WL, Lin YJ, Chang JG, Tsai FJ. Chen YT, et al. Among authors: lin yj, lin wd. Oncotarget. 2015 May 30;6(15):12997-3005. doi: 10.18632/oncotarget.4092. Oncotarget. 2015. PMID: 26079428 Free PMC article.

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