Hu L - Search Results

1

Phenotypic characterization of missense polymerase-δ mutations using an inducible protein-replacement system.

Ghodgaonkar MM, Kehl P, Ventura I, Hu L, Bignami M, Jiricny J. Ghodgaonkar MM, et al. Among authors: hu l. Nat Commun. 2014 Sep 22;5:4990. doi: 10.1038/ncomms5990. Nat Commun. 2014. PMID: 25241845 Free article.

2

Unstable argininosuccinate lyase in variant forms of the urea cycle disorder argininosuccinic aciduria.

Hu L, Pandey AV, Balmer C, Eggimann S, Rüfenacht V, Nuoffer JM, Häberle J. Hu L, et al. J Inherit Metab Dis. 2015 Sep;38(5):815-27. doi: 10.1007/s10545-014-9807-3. Epub 2015 Mar 17. J Inherit Metab Dis. 2015. PMID: 25778938 Free article.

3

Phytohemagglutinin stimulation of lymphocytes improves mutation analysis of carbamoylphosphate synthetase 1.

Kretz R, Hu L, Wettstein V, Leiteritz D, Häberle J. Kretz R, et al. Among authors: hu l. Mol Genet Metab. 2012 Jul;106(3):375-8. doi: 10.1016/j.ymgme.2012.04.011. Epub 2012 Apr 23. Mol Genet Metab. 2012. PMID: 22575620

4

Understanding the role of argininosuccinate lyase transcript variants in the clinical and biochemical variability of the urea cycle disorder argininosuccinic aciduria.

Hu L, Pandey AV, Eggimann S, Rüfenacht V, Möslinger D, Nuoffer JM, Häberle J. Hu L, et al. J Biol Chem. 2013 Nov 29;288(48):34599-611. doi: 10.1074/jbc.M113.503128. Epub 2013 Oct 17. J Biol Chem. 2013. PMID: 24136197 Free PMC article.

5

Understanding carbamoyl phosphate synthetase (CPS1) deficiency by using the recombinantly purified human enzyme: effects of CPS1 mutations that concentrate in a central domain of unknown function.

Díez-Fernández C, Hu L, Cervera J, Häberle J, Rubio V. Díez-Fernández C, et al. Among authors: hu l. Mol Genet Metab. 2014 Jun;112(2):123-32. doi: 10.1016/j.ymgme.2014.04.003. Epub 2014 Apr 18. Mol Genet Metab. 2014. PMID: 24813853 Free article.

6

Effect of Cysteamine on Mutant ASL Proteins with Cysteine for Arginine Substitutions.

Inauen C, Rüfenacht V, Pandey AV, Hu L, Blom H, Nuoffer JM, Häberle J. Inauen C, et al. Among authors: hu l. Mol Diagn Ther. 2016 Apr;20(2):125-33. doi: 10.1007/s40291-015-0182-z. Mol Diagn Ther. 2016. PMID: 26745957

7

Secondary NAD+ deficiency in the inherited defect of glutamine synthetase.

Hu L, Ibrahim K, Stucki M, Frapolli M, Shahbeck N, Chaudhry FA, Görg B, Häussinger D, Penberthy WT, Ben-Omran T, Häberle J. Hu L, et al. J Inherit Metab Dis. 2015 Nov;38(6):1075-83. doi: 10.1007/s10545-015-9846-4. Epub 2015 Apr 21. J Inherit Metab Dis. 2015. PMID: 25896882 Free article.

8

Pan-Cancer Proteomics Analysis Reveals Wiskott-Aldrich Syndrome Protein as a Potential Regulator of Programmed Death-Ligand 1.

Hu L, Liu D, Zheng D, Lu J, Yuan X, Li Y, Shi F, Shi X, He QY, Li Q, Zhang CZ. Hu L, et al. J Proteome Res. 2024 Apr 25. doi: 10.1021/acs.jproteome.4c00124. Online ahead of print. J Proteome Res. 2024. PMID: 38661673

9

[Moxifloxacin treatment for Mycoplasma hominis meningitis in an extremely preterm infant].

Mao WY, Lan JE, Gan MY, Zhang XJ, Yu H, Hu LY, Zhang R, Cao Y, Xiao ML. Mao WY, et al. Among authors: hu ly. Zhongguo Dang Dai Er Ke Za Zhi. 2024 Apr 15;26(4):432-436. doi: 10.7499/j.issn.1008-8830.2312016. Zhongguo Dang Dai Er Ke Za Zhi. 2024. PMID: 38660910 Chinese.

10

Newly formed dust within the circumstellar environment of SN Ia-CSM 2018evt.

Wang王 L灵, Hu M, Wang L, Yang 杨 Y轶, Yang J, Gomez H, Chen S, Hu L, Chen TW, Mo J, Wang X, Baade D, Hoeflich P, Wheeler JC, Pignata G, Burke J, Hiramatsu D, Howell DA, McCully C, Pellegrino C, Galbany L, Hsiao EY, Sand DJ, Zhang J, Uddin SA, Anderson JP, Ashall C, Cheng C, Gromadzki M, Inserra C, Lin H, Morrell N, Morales-Garoffolo A, Müller-Bravo TE, Nicholl M, Gonzalez EP, Phillips MM, Pineda-García J, Sai H, Smith M, Shahbandeh M, Srivastav S, Stritzinger MD, Yang S, Young DR, Yu L, Zhang X. Wang王 L灵, et al. Among authors: hu l. Nat Astron. 2024;8(4):504-519. doi: 10.1038/s41550-024-02197-9. Epub 2024 Feb 9. Nat Astron. 2024. PMID: 38659610 Free PMC article.

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