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Nazneen Rahman

Showing results (51-60 of 154) with videos related to

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The Journal of Clinical Investigation|July 24, 2018
Mosaic-variegated aneuploidy syndrome mutation or haploinsufficiency in Cep57 impairs tumor suppressionKhaled Aziz, Cynthia J Sieben, Karthik B Jeganathan, et al.
Journal of Health, Population, and Nutrition|November 15, 2014
Recognition of and Response to neonatal intrapartum-related complications in home-birth settings in BangladeshKristin E VanderEnde, Allisyn C Moran, Karen Leasure, et al.
Current Topics in Medicinal Chemistry|April 27, 2022
Solanum pubescens Wild Fruits Essential Oil - A Golden Casket for its Antimicrobial and Anti-inflammatory Mediated Wound Healing Efficacy in Vertebrate Model Mus musculusHaseebur Rahman, Nazneen Rahman, Mir Haris, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 10, 2010
Generation of trisomies in cancer cells by multipolar mitosis and incomplete cytokinesisDavid Gisselsson, Yuesheng Jin, David Lindgren, et al.
Cancer Research|December 26, 2003
Evaluation of Fanconi Anemia genes in familial breast cancer predispositionSheila Seal, Rita Barfoot, Hiran Jayatilake, et al.
Human Mutation|March 14, 2013
Simple detection of germline microsatellite instability for diagnosis of constitutional mismatch repair cancer syndromeDanielle Ingham, Christine P Diggle, Ian Berry, et al.
Breast Cancer Research and Treatment|June 1, 2010
Mutation and association analysis of GEN1 in breast cancer susceptibilityClare Turnbull, Sarah Hines, Anthony Renwick, et al.
Scientific Reports|July 14, 2016
Implementing rapid, robust, cost-effective, patient-centred, routine genetic testing in ovarian cancer patientsAngela George, Daniel Riddell, Sheila Seal, et al.
American Journal of Medical Genetics. Part A|October 14, 2005
Familial gigantism caused by an NSD1 mutationMieke M van Haelst, Jeannette J M Hoogeboom, Genevieve Baujat, et al.
Human Molecular Genetics|May 15, 2015
Mutations in the PP2A regulatory subunit B family genes PPP2R5B, PPP2R5C and PPP2R5D cause human overgrowthChey Loveday, Katrina Tatton-Brown, Matthew Clarke, et al.
Pageof 16

Showing results (51-60 of 154) with videos related to

Sort By:
Pageof 16
The Journal of Clinical Investigation|July 24, 2018
Mosaic-variegated aneuploidy syndrome mutation or haploinsufficiency in Cep57 impairs tumor suppressionKhaled Aziz, Cynthia J Sieben, Karthik B Jeganathan, et al.
Journal of Health, Population, and Nutrition|November 15, 2014
Recognition of and Response to neonatal intrapartum-related complications in home-birth settings in BangladeshKristin E VanderEnde, Allisyn C Moran, Karen Leasure, et al.
Current Topics in Medicinal Chemistry|April 27, 2022
Solanum pubescens Wild Fruits Essential Oil - A Golden Casket for its Antimicrobial and Anti-inflammatory Mediated Wound Healing Efficacy in Vertebrate Model Mus musculusHaseebur Rahman, Nazneen Rahman, Mir Haris, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 10, 2010
Generation of trisomies in cancer cells by multipolar mitosis and incomplete cytokinesisDavid Gisselsson, Yuesheng Jin, David Lindgren, et al.
Cancer Research|December 26, 2003
Evaluation of Fanconi Anemia genes in familial breast cancer predispositionSheila Seal, Rita Barfoot, Hiran Jayatilake, et al.
Human Mutation|March 14, 2013
Simple detection of germline microsatellite instability for diagnosis of constitutional mismatch repair cancer syndromeDanielle Ingham, Christine P Diggle, Ian Berry, et al.
Breast Cancer Research and Treatment|June 1, 2010
Mutation and association analysis of GEN1 in breast cancer susceptibilityClare Turnbull, Sarah Hines, Anthony Renwick, et al.
Scientific Reports|July 14, 2016
Implementing rapid, robust, cost-effective, patient-centred, routine genetic testing in ovarian cancer patientsAngela George, Daniel Riddell, Sheila Seal, et al.
American Journal of Medical Genetics. Part A|October 14, 2005
Familial gigantism caused by an NSD1 mutationMieke M van Haelst, Jeannette J M Hoogeboom, Genevieve Baujat, et al.
Human Molecular Genetics|May 15, 2015
Mutations in the PP2A regulatory subunit B family genes PPP2R5B, PPP2R5C and PPP2R5D cause human overgrowthChey Loveday, Katrina Tatton-Brown, Matthew Clarke, et al.
Pageof 16