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L Sherman

Showing results (861-870 of 935) with videos related to

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Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|December 30, 2016
The DART Study: Results from the Dose-Escalation and Expansion Cohorts Evaluating the Combination of Dalantercept plus Axitinib in Advanced Renal Cell CarcinomaMartin H Voss, Rupal S Bhatt, Elizabeth R Plimack, et al.
Journal of the National Cancer Institute|April 1, 2015
Annual Report to the Nation on the Status of Cancer, 1975-2011, Featuring Incidence of Breast Cancer Subtypes by Race/Ethnicity, Poverty, and StateBetsy A Kohler, Recinda L Sherman, Nadia Howlader, et al.
American Journal of Medical Genetics. Part A|February 28, 2013
Fragile X AGG analysis provides new risk predictions for 45-69 repeat allelesSarah L Nolin, Sachin Sah, Anne Glicksman, et al.
Elife|March 5, 2020
Proteome profile of peripheral myelin in healthy mice and in a neuropathy modelSophie B Siems, Olaf Jahn, Maria A Eichel, et al.
Human Molecular Genetics|August 21, 2018
Homozygous mutation in the Neurofascin gene affecting the glial isoform of Neurofascin causes severe neurodevelopment disorder with hypotonia, amimia and areflexiaRobert Smigiel, Diane L Sherman, Malgorzata Rydzanicz, et al.
Cancer|March 13, 2020
Annual report to the nation on the status of cancer, part II: Progress toward Healthy People 2020 objectives for 4 common cancersS Jane Henley, Cheryll C Thomas, Denise Riedel Lewis, et al.
Nature Genetics|December 1, 1996
Susceptible chiasmate configurations of chromosome 21 predispose to non-disjunction in both maternal meiosis I and meiosis IIN E Lamb, S B Freeman, A Savage-Austin, et al.
American Journal of Medical Genetics. Part A|February 13, 2013
Preconception folic acid supplementation and risk for chromosome 21 nondisjunction: a report from the National Down Syndrome ProjectNaTasha D Hollis, Emily G Allen, Tiffany Renee Oliver, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|October 12, 2011
Lack of maternal folic acid supplementation is associated with heart defects in Down syndrome: a report from the National Down Syndrome ProjectLora J H Bean, Emily G Allen, Stuart W Tinker, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 24, 2014
Contribution of copy-number variation to Down syndrome-associated atrioventricular septal defectsDhanya Ramachandran, Jennifer G Mulle, Adam E Locke, et al.
Pageof 94

Showing results (861-870 of 935) with videos related to

Sort By:
Pageof 94
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|December 30, 2016
The DART Study: Results from the Dose-Escalation and Expansion Cohorts Evaluating the Combination of Dalantercept plus Axitinib in Advanced Renal Cell CarcinomaMartin H Voss, Rupal S Bhatt, Elizabeth R Plimack, et al.
Journal of the National Cancer Institute|April 1, 2015
Annual Report to the Nation on the Status of Cancer, 1975-2011, Featuring Incidence of Breast Cancer Subtypes by Race/Ethnicity, Poverty, and StateBetsy A Kohler, Recinda L Sherman, Nadia Howlader, et al.
American Journal of Medical Genetics. Part A|February 28, 2013
Fragile X AGG analysis provides new risk predictions for 45-69 repeat allelesSarah L Nolin, Sachin Sah, Anne Glicksman, et al.
Elife|March 5, 2020
Proteome profile of peripheral myelin in healthy mice and in a neuropathy modelSophie B Siems, Olaf Jahn, Maria A Eichel, et al.
Human Molecular Genetics|August 21, 2018
Homozygous mutation in the Neurofascin gene affecting the glial isoform of Neurofascin causes severe neurodevelopment disorder with hypotonia, amimia and areflexiaRobert Smigiel, Diane L Sherman, Malgorzata Rydzanicz, et al.
Cancer|March 13, 2020
Annual report to the nation on the status of cancer, part II: Progress toward Healthy People 2020 objectives for 4 common cancersS Jane Henley, Cheryll C Thomas, Denise Riedel Lewis, et al.
Nature Genetics|December 1, 1996
Susceptible chiasmate configurations of chromosome 21 predispose to non-disjunction in both maternal meiosis I and meiosis IIN E Lamb, S B Freeman, A Savage-Austin, et al.
American Journal of Medical Genetics. Part A|February 13, 2013
Preconception folic acid supplementation and risk for chromosome 21 nondisjunction: a report from the National Down Syndrome ProjectNaTasha D Hollis, Emily G Allen, Tiffany Renee Oliver, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|October 12, 2011
Lack of maternal folic acid supplementation is associated with heart defects in Down syndrome: a report from the National Down Syndrome ProjectLora J H Bean, Emily G Allen, Stuart W Tinker, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 24, 2014
Contribution of copy-number variation to Down syndrome-associated atrioventricular septal defectsDhanya Ramachandran, Jennifer G Mulle, Adam E Locke, et al.
Pageof 94