Battaile KP - Search Results

1

Signal transfer in human protein tyrosine phosphatase PTP1B from allosteric inhibitor P00058.

Chirgadze YN, Battaile KP, Likhachev IV, Balabaev NK, Gordon RD, Romanov V, Lin A, Karisch R, Lam R, Ruzanov M, Brazhnikov EV, Pai EF, Neel BG, Chirgadze NY. Chirgadze YN, et al. Among authors: battaile kp. J Biomol Struct Dyn. 2022;40(24):13823-13832. doi: 10.1080/07391102.2021.1994879. Epub 2021 Oct 27. J Biomol Struct Dyn. 2022. PMID: 34705594

2

Pseudomonas aeruginosa Dps (PA0962) Functions in H₂O₂ Mediated Oxidative Stress Defense and Exhibits In Vitro DNA Cleaving Activity.

Rajapaksha N, Soldano A, Yao H, Donnarumma F, Kashipathy MM, Seibold S, Battaile KP, Lovell S, Rivera M. Rajapaksha N, et al. Among authors: battaile kp. Int J Mol Sci. 2023 Feb 28;24(5):4669. doi: 10.3390/ijms24054669. Int J Mol Sci. 2023. PMID: 36902100 Free PMC article.

3

Fanconi anemia group A and C double-mutant mice: functional evidence for a multi-protein Fanconi anemia complex.

Noll M, Battaile KP, Bateman R, Lax TP, Rathbun K, Reifsteck C, Bagby G, Finegold M, Olson S, Grompe M. Noll M, et al. Among authors: battaile kp. Exp Hematol. 2002 Jul;30(7):679-88. doi: 10.1016/s0301-472x(02)00838-x. Exp Hematol. 2002. PMID: 12135664 Free article.

4

Fetal demise with Smith-Lemli-Opitz syndrome confirmed by tissue sterol analysis and the absence of measurable 7-dehydrocholesterol Delta(7)-reductase activity in chorionic villi.

Linck LM, Hayflick SJ, Lin DS, Battaile KP, Ginat S, Burlingame T, Gibson KM, Honda M, Honda A, Salen G, Tint GS, Connor WE, Steiner RD. Linck LM, et al. Among authors: battaile kp. Prenat Diagn. 2000 Mar;20(3):238-40. Prenat Diagn. 2000. PMID: 10719329

5

An African-Specific Variant of TP53 Reveals PADI4 as a Regulator of p53-Mediated Tumor Suppression.

Indeglia A, Leung JC, Miller SA, Leu JI, Dougherty JF, Clarke NL, Kirven NA, Shao C, Ke L, Lovell S, Barnoud T, Lu DY, Lin C, Kannan T, Battaile KP, Yang THL, Batista Oliva I, Claiborne DT, Vogel P, Liu L, Liu Q, Nefedova Y, Cassel J, Auslander N, Kossenkov AV, Karanicolas J, Murphy ME. Indeglia A, et al. Among authors: battaile kp. Cancer Discov. 2023 Jul 7;13(7):1696-1719. doi: 10.1158/2159-8290.CD-22-1315. Cancer Discov. 2023. PMID: 37140445 Free PMC article.

6

Smith-Lemli-Opitz syndrome: the first malformation syndrome associated with defective cholesterol synthesis.

Battaile KP, Steiner RD. Battaile KP, et al. Mol Genet Metab. 2000 Sep-Oct;71(1-2):154-62. doi: 10.1006/mgme.2000.3020. Mol Genet Metab. 2000. PMID: 11001806 Review.

7

Mutation analysis and description of sixteen RSH/Smith-Lemli-Opitz syndrome patients: polymerase chain reaction-based assays to simplify genotyping.

Krakowiak PA, Nwokoro NA, Wassif CA, Battaile KP, Nowaczyk MJ, Connor WE, Maslen C, Steiner RD, Porter FD. Krakowiak PA, et al. Among authors: battaile kp. Am J Med Genet. 2000 Sep 18;94(3):214-27. Am J Med Genet. 2000. PMID: 10995508

8

In vivo selection of wild-type hematopoietic stem cells in a murine model of Fanconi anemia.

Battaile KP, Bateman RL, Mortimer D, Mulcahy J, Rathbun RK, Bagby G, Fleming WH, Grompe M. Battaile KP, et al. Blood. 1999 Sep 15;94(6):2151-8. Blood. 1999. PMID: 10477746 Free article.

9

Biochemical, phenotypic and neurophysiological characterization of a genetic mouse model of RSH/Smith--Lemli--Opitz syndrome.

Wassif CA, Zhu P, Kratz L, Krakowiak PA, Battaile KP, Weight FF, Grinberg A, Steiner RD, Nwokoro NA, Kelley RI, Stewart RR, Porter FD. Wassif CA, et al. Among authors: battaile kp. Hum Mol Genet. 2001 Mar 15;10(6):555-64. doi: 10.1093/hmg/10.6.555. Hum Mol Genet. 2001. PMID: 11230174

10

A simple PCR-based assay allows detection of a common mutation, IVS8-1G-->C, in DHCR7 in Smith-Lemli-Opitz syndrome.

Battaile KP, Maslen CL, Wassif CA, Krakowiak P, Porter FD, Steiner RD. Battaile KP, et al. Genet Test. 1999;3(4):361-3. doi: 10.1089/gte.1999.3.361. Genet Test. 1999. PMID: 10627944

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