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Kristen M Pike

Showing results (1-10 of 8) with videos related to

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Journal of Medical Genetics|April 24, 2026
VHL gene fragment analysis: large inversion detection in <i>Alu</i> region for clinical applicationsRyan N Baugher, Stephanie D Mellott, Kristen M Pike, et al.
Journal of Clinical Laboratory Analysis|March 30, 2026
UGT1A1 Fragment Analysis: Genotyping the (TA)<sub>n</sub> Variable Repeat Polymorphism for Clinical ApplicationsRyan N Baugher, Kristen M Pike, Teri M Plona, et al.
Familial Cancer|May 27, 2011
Lack of germline PALB2 mutations in melanoma-prone families with CDKN2A mutations and pancreatic cancerXiaohong R Yang, Lea Jessop, Timothy Myers, et al.
The New England Journal of Medicine|December 31, 2010
Residual NADPH oxidase and survival in chronic granulomatous diseaseDouglas B Kuhns, W Gregory Alvord, Theo Heller, et al.
International Journal of Molecular Sciences|February 6, 2020
Comparison of Eight Technologies to Determine Genotype at the UGT1A1 (TA)<sub>n</sub> Repeat Polymorphism: Potential Clinical Consequences of Genotyping Errors?Tristan M Sissung, Roberto H Barbier, Douglas K Price, et al.
Journal of Medical Genetics|November 25, 2010
Cancer and neurologic degeneration in xeroderma pigmentosum: long term follow-up characterises the role of DNA repairPorcia T Bradford, Alisa M Goldstein, Deborah Tamura, et al.
Cell Death & Disease|September 7, 2021
A novel mouse model of PMS2 founder mutation that causes mismatch repair defect due to aberrant splicingKajal Biswas, Martin Couillard, Luca Cavallone, et al.
Journal of Clinical Pharmacology|September 19, 2017
Pharmacogenomics Implementation at the National Institutes of Health Clinical CenterTristan M Sissung, Jon W McKeeby, Jharana Patel, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Journal of Medical Genetics|April 24, 2026
VHL gene fragment analysis: large inversion detection in <i>Alu</i> region for clinical applicationsRyan N Baugher, Stephanie D Mellott, Kristen M Pike, et al.
Journal of Clinical Laboratory Analysis|March 30, 2026
UGT1A1 Fragment Analysis: Genotyping the (TA)<sub>n</sub> Variable Repeat Polymorphism for Clinical ApplicationsRyan N Baugher, Kristen M Pike, Teri M Plona, et al.
Familial Cancer|May 27, 2011
Lack of germline PALB2 mutations in melanoma-prone families with CDKN2A mutations and pancreatic cancerXiaohong R Yang, Lea Jessop, Timothy Myers, et al.
The New England Journal of Medicine|December 31, 2010
Residual NADPH oxidase and survival in chronic granulomatous diseaseDouglas B Kuhns, W Gregory Alvord, Theo Heller, et al.
International Journal of Molecular Sciences|February 6, 2020
Comparison of Eight Technologies to Determine Genotype at the UGT1A1 (TA)<sub>n</sub> Repeat Polymorphism: Potential Clinical Consequences of Genotyping Errors?Tristan M Sissung, Roberto H Barbier, Douglas K Price, et al.
Journal of Medical Genetics|November 25, 2010
Cancer and neurologic degeneration in xeroderma pigmentosum: long term follow-up characterises the role of DNA repairPorcia T Bradford, Alisa M Goldstein, Deborah Tamura, et al.
Cell Death & Disease|September 7, 2021
A novel mouse model of PMS2 founder mutation that causes mismatch repair defect due to aberrant splicingKajal Biswas, Martin Couillard, Luca Cavallone, et al.
Journal of Clinical Pharmacology|September 19, 2017
Pharmacogenomics Implementation at the National Institutes of Health Clinical CenterTristan M Sissung, Jon W McKeeby, Jharana Patel, et al.
Pageof 1