Year |
Citation |
Score |
2009 |
Claassen DA, Desler MM, Rizzino A. ROCK inhibition enhances the recovery and growth of cryopreserved human embryonic stem cells and human induced pluripotent stem cells. Molecular Reproduction and Development. 76: 722-32. PMID 19235204 DOI: 10.1002/Mrd.21021 |
0.598 |
|
2007 |
Claassen DA, Lahue RS. Expansions of CAG.CTG repeats in immortalized human astrocytes. Human Molecular Genetics. 16: 3088-96. PMID 17881653 DOI: 10.1093/Hmg/Ddm270 |
0.37 |
|
Low-probability matches (unlikely to be authored by this person) |
2004 |
Huizing M, Hess R, Dorward H, Claassen DA, Helip-Wooley A, Kleta R, Kaiser-Kupfer MI, White JG, Gahl WA. Cellular, molecular and clinical characterization of patients with Hermansky-Pudlak syndrome type 5. Traffic (Copenhagen, Denmark). 5: 711-22. PMID 15296495 DOI: 10.1111/J.1600-0854.2004.00208.X |
0.288 |
|
2003 |
Anderson PD, Huizing M, Claassen DA, White J, Gahl WA. Hermansky-Pudlak syndrome type 4 (HPS-4): clinical and molecular characteristics. Human Genetics. 113: 10-7. PMID 12664304 DOI: 10.1007/S00439-003-0933-5 |
0.267 |
|
2005 |
Griffin AE, Cobb BR, Anderson PD, Claassen DA, Helip-Wooley A, Huizing M, Gahl WA. Detection of hemizygosity in Hermansky - Pudlak syndrome by quantitative real-time PCR Clinical Genetics. 68: 23-30. PMID 15952982 DOI: 10.1111/J.1399-0004.2005.00461.X |
0.245 |
|
2009 |
Boer B, Cox JL, Claassen D, Mallanna SK, Desler M, Rizzino A. Regulation of the Nanog gene by both positive and negative cis-regulatory elements in embryonal carcinoma cells and embryonic stem cells. Molecular Reproduction and Development. 76: 173-82. PMID 18537119 DOI: 10.1002/Mrd.20943 |
0.215 |
|
2003 |
Huizing M, Helip-Wooley A, Dorward H, Claassen D, Hess R, Gahl WA. IL-25 Hermansky-Pudlak syndrome: a model for abnormal vesicle formation and trafficking Pigment Cell Research. 16: 584-584. DOI: 10.1034/J.1600-0749.2003.08341.X |
0.173 |
|
2022 |
Ibrahim A, Sharathkumar A, McLaughlin H, Claassen D, Bhagavathi S. Congenital Neutropenia with Specific Granulocyte Deficiency Caused by Novel Double Heterozygous Mutations. Hematology Reports. 14: 270-275. PMID 36135322 DOI: 10.3390/hematolrep14030038 |
0.116 |
|
2018 |
Claassen D, Boals M, Bowling KM, Cooper GM, Cox J, Hershfield M, Lewis S, Wlodarski M, Weiss MJ, Estepp JH. Complexities of genetic diagnosis illustrated by an atypical case of congenital hypoplastic anemia. Cold Spring Harbor Molecular Case Studies. 4. PMID 30559313 DOI: 10.1101/mcs.a003384 |
0.096 |
|
1995 |
De Graaf AS, Lombard CJ, Claassen DA. Influence of ethnic and geographic factors on the classic photoparoxysmal response in the electroencephalogram of epilepsy patients Epilepsia. 36: 219-223. PMID 7614903 DOI: 10.1111/j.1528-1157.1995.tb00987.x |
0.047 |
|
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