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Michael Field

Showing results (71-80 of 136) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 30, 2016
Streamlined genetic education is effective in preparing women newly diagnosed with breast cancer for decision making about treatment-focused genetic testing: a randomized controlled noninferiority trialVeronica F Quinn, Bettina Meiser, Judy Kirk, et al.
Mucosal Immunology|August 17, 2018
High-dimensional immune phenotyping and transcriptional analyses reveal robust recovery of viable human immune and epithelial cells from frozen gastrointestinal tissueLiza Konnikova, Gilles Boschetti, Adeeb Rahman, et al.
Elife|July 6, 2017
Macrophage dysfunction initiates colitis during weaning of infant mice lacking the interleukin-10 receptorNaresh S Redhu, Vasudevan Bakthavatchalu, Evan A Conaway, et al.
Nature Communications|May 5, 2018
WASP-mediated regulation of anti-inflammatory macrophages is IL-10 dependent and is critical for intestinal homeostasisAmlan Biswas, Dror S Shouval, Alexandra Griffith, et al.
Scientific Reports|July 18, 2020
FMR1 mRNA from full mutation alleles is associated with ABC-C<sub>FX</sub> scores in males with fragile X syndromeEmma K Baker, Marta Arpone, Claudine Kraan, et al.
American Journal of Human Genetics|September 25, 2012
A noncoding, regulatory mutation implicates HCFC1 in nonsyndromic intellectual disabilityLingli Huang, Lachlan A Jolly, Saffron Willis-Owen, et al.
Human Mutation|May 8, 2007
Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardationReinhard Ullmann, Gillian Turner, Maria Kirchhoff, et al.
Digestive Diseases and Sciences|February 28, 2018
Genetic and Structural Analysis of a SKIV2L Mutation Causing Tricho-hepato-enteric SyndromeIddo Vardi, Ortal Barel, Michal Sperber, et al.
Oncotarget|March 1, 2018
Rapid detection of <i>BRCA1/2</i> recurrent mutations in Chinese breast and ovarian cancer patients with multiplex SNaPshot genotyping panelsAva Kwong, John C W Ho, Vivian Y Shin, et al.
Plos Genetics|June 23, 2009
Disease-causing 7.4 kb cis-regulatory deletion disrupting conserved non-coding sequences and their interaction with the FOXL2 promotor: implications for mutation screeningBarbara D'haene, Catia Attanasio, Diane Beysen, et al.
Pageof 14

Showing results (71-80 of 136) with videos related to

Sort By:
Pageof 14
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 30, 2016
Streamlined genetic education is effective in preparing women newly diagnosed with breast cancer for decision making about treatment-focused genetic testing: a randomized controlled noninferiority trialVeronica F Quinn, Bettina Meiser, Judy Kirk, et al.
Mucosal Immunology|August 17, 2018
High-dimensional immune phenotyping and transcriptional analyses reveal robust recovery of viable human immune and epithelial cells from frozen gastrointestinal tissueLiza Konnikova, Gilles Boschetti, Adeeb Rahman, et al.
Elife|July 6, 2017
Macrophage dysfunction initiates colitis during weaning of infant mice lacking the interleukin-10 receptorNaresh S Redhu, Vasudevan Bakthavatchalu, Evan A Conaway, et al.
Nature Communications|May 5, 2018
WASP-mediated regulation of anti-inflammatory macrophages is IL-10 dependent and is critical for intestinal homeostasisAmlan Biswas, Dror S Shouval, Alexandra Griffith, et al.
Scientific Reports|July 18, 2020
FMR1 mRNA from full mutation alleles is associated with ABC-C<sub>FX</sub> scores in males with fragile X syndromeEmma K Baker, Marta Arpone, Claudine Kraan, et al.
American Journal of Human Genetics|September 25, 2012
A noncoding, regulatory mutation implicates HCFC1 in nonsyndromic intellectual disabilityLingli Huang, Lachlan A Jolly, Saffron Willis-Owen, et al.
Human Mutation|May 8, 2007
Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardationReinhard Ullmann, Gillian Turner, Maria Kirchhoff, et al.
Digestive Diseases and Sciences|February 28, 2018
Genetic and Structural Analysis of a SKIV2L Mutation Causing Tricho-hepato-enteric SyndromeIddo Vardi, Ortal Barel, Michal Sperber, et al.
Oncotarget|March 1, 2018
Rapid detection of <i>BRCA1/2</i> recurrent mutations in Chinese breast and ovarian cancer patients with multiplex SNaPshot genotyping panelsAva Kwong, John C W Ho, Vivian Y Shin, et al.
Plos Genetics|June 23, 2009
Disease-causing 7.4 kb cis-regulatory deletion disrupting conserved non-coding sequences and their interaction with the FOXL2 promotor: implications for mutation screeningBarbara D'haene, Catia Attanasio, Diane Beysen, et al.
Pageof 14