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Items: 15

1.

Probing the dynamics of nanoparticle formation from a precursor at atomic resolution.

Gao W, Tieu P, Addiego C, Ma Y, Wu J, Pan X.

Sci Adv. 2019 Jan 25;5(1):eaau9590. doi: 10.1126/sciadv.aau9590. eCollection 2019 Jan.

2.

CATP-6, a C. elegans ortholog of ATP13A2 PARK9, positively regulates GEM-1, an SLC16A transporter.

Lambie EJ, Tieu PJ, Lebedeva N, Church DL, Conradt B.

PLoS One. 2013 Oct 9;8(10):e77202. doi: 10.1371/journal.pone.0077202. eCollection 2013.

3.

Assessing sub-optimal performance with the Test of Memory Malingering in Spanish speaking patients with TBI.

Strutt AM, Scott BM, Lozano VJ, Tieu PG, Peery S.

Brain Inj. 2012;26(6):853-63. doi: 10.3109/02699052.2012.655366.

PMID:
22583176
4.

The impact of a standardized patient program on student learning of communication skills.

Rickles NM, Tieu P, Myers L, Galal S, Chung V.

Am J Pharm Educ. 2009 Feb 19;73(1):4.

5.

In vivo construction of recombinant molecules within the Caenorhabditis elegans germ line using short regions of terminal homology.

Kemp BJ, Hatzold J, Sternick LA, Cornman-Homonoff J, Whitaker JM, Tieu PJ, Lambie EJ.

Nucleic Acids Res. 2007;35(19):e133. Epub 2007 Oct 11.

6.

NAGLU mutations underlying Sanfilippo syndrome type B.

Schmidtchen A, Greenberg D, Zhao HG, Li HH, Huang Y, Tieu P, Zhao HZ, Cheng S, Zhao Z, Whitley CB, Di Natale P, Neufeld EF.

Am J Hum Genet. 1998 Jan;62(1):64-9.

7.

Four novel mutations underlying mild or intermediate forms of alpha-L-iduronidase deficiency (MPS IS and MPS IH/S).

Tieu PT, Bach G, Matynia A, Hwang M, Neufeld EF.

Hum Mutat. 1995;6(1):55-9.

PMID:
7550232
8.

A mutant stop codon (TAG) in the IDUA gene is used as an acceptor splice site in a patient with Hurler syndrome (MPS IH).

Tieu PT, Menon K, Neufeld EF.

Hum Mutat. 1994;3(3):333-6. No abstract available.

PMID:
8019572
9.
10.

Individual and community characteristics influencing breastfeeding duration in Vietnam.

Swenson IE, Thang NM, Tieu PX.

Ann Hum Biol. 1993 Jul-Aug;20(4):325-34.

PMID:
8346893
11.

Factors related to the utilization of prenatal care in Vietnam.

Swenson IE, Thang NM, Nhan VQ, Tieu PX.

J Trop Med Hyg. 1993 Apr;96(2):76-85.

PMID:
8096252
12.

A deletion/insertion mutation in the IDUA gene in a Libyan Jewish patient with Hurler syndrome (mucopolysaccharidosis IH).

Moskowitz SM, Tieu PT, Neufeld EF.

Hum Mutat. 1993;2(1):71-3. No abstract available.

PMID:
8477267
13.

Mutation in Scheie syndrome (MPS IS): a G-->A transition creates new splice site in intron 5 of one IDUA allele.

Moskowitz SM, Tieu PT, Neufeld EF.

Hum Mutat. 1993;2(2):141-4. No abstract available.

PMID:
8318992
14.

Architecture of the canine IDUA gene and mutation underlying canine mucopolysaccharidosis I.

Menon KP, Tieu PT, Neufeld EF.

Genomics. 1992 Nov;14(3):763-8.

PMID:
1339393
15.

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