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Alka Dwivedi

Showing results (21-30 of 37) with videos related to

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RSC Advances|July 16, 2019
Hydrogel scaffold with substrate elasticity mimicking physiological-niche promotes proliferation of functional keratinocytesPankaj Mogha, Ankita Srivastava, Sushant Kumar, et al.
Human Genetics|February 1, 2014
Clinical and genomic evaluation of 201 patients with Phelan-McDermid syndromeSara M Sarasua, Luigi Boccuto, Julia L Sharp, et al.
American Journal of Physiology. Gastrointestinal and Liver Physiology|August 2, 2008
Serotonin modifies cytoskeleton and brush-border membrane architecture in human intestinal epithelial cellsRavinder K Gill, Le Shen, Jerrold R Turner, et al.
Journal of Medical Genetics|October 11, 2011
Association between deletion size and important phenotypes expands the genomic region of interest in Phelan-McDermid syndrome (22q13 deletion syndrome)Sara M Sarasua, Alka Dwivedi, Luigi Boccuto, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 19, 2013
22q13.2q13.32 genomic regions associated with severity of speech delay, developmental delay, and physical features in Phelan-McDermid syndromeSara M Sarasua, Alka Dwivedi, Luigi Boccuto, et al.
Journal of Immunology (Baltimore, Md. : 1950)|February 15, 2019
Differential Influence of IL-9 and IL-17 on Actin Cytoskeleton Regulates the Migration Potential of Human KeratinocytesSreya Das, Srisathya Srinivasan, Ankita Srivastava, et al.
European Journal of Human Genetics : EJHG|June 2, 2011
17p13.3 microduplications are associated with split-hand/foot malformation and long-bone deficiency (SHFLD)Christine M Armour, Dennis E Bulman, Olga Jarinova, et al.
Molecular Cancer Research : MCR|January 31, 2020
The Th9 Axis Reduces the Oxidative Stress and Promotes the Survival of Malignant T Cells in Cutaneous T-Cell Lymphoma PatientsSushant Kumar, Bhavuk Dhamija, Soumitra Marathe, et al.
Journal of Medical Genetics|June 3, 2015
Microdeletions on 6p22.3 are associated with mesomelic dysplasia Savarirayan typeRicarda Flöttmann, Johannes Wagner, Karolina Kobus, et al.
European Journal of Human Genetics : EJHG|August 16, 2012
Prevalence of SHANK3 variants in patients with different subtypes of autism spectrum disordersLuigi Boccuto, Maria Lauri, Sara M Sarasua, et al.
Pageof 4

Showing results (21-30 of 37) with videos related to

Sort By:
Pageof 4
RSC Advances|July 16, 2019
Hydrogel scaffold with substrate elasticity mimicking physiological-niche promotes proliferation of functional keratinocytesPankaj Mogha, Ankita Srivastava, Sushant Kumar, et al.
Human Genetics|February 1, 2014
Clinical and genomic evaluation of 201 patients with Phelan-McDermid syndromeSara M Sarasua, Luigi Boccuto, Julia L Sharp, et al.
American Journal of Physiology. Gastrointestinal and Liver Physiology|August 2, 2008
Serotonin modifies cytoskeleton and brush-border membrane architecture in human intestinal epithelial cellsRavinder K Gill, Le Shen, Jerrold R Turner, et al.
Journal of Medical Genetics|October 11, 2011
Association between deletion size and important phenotypes expands the genomic region of interest in Phelan-McDermid syndrome (22q13 deletion syndrome)Sara M Sarasua, Alka Dwivedi, Luigi Boccuto, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 19, 2013
22q13.2q13.32 genomic regions associated with severity of speech delay, developmental delay, and physical features in Phelan-McDermid syndromeSara M Sarasua, Alka Dwivedi, Luigi Boccuto, et al.
Journal of Immunology (Baltimore, Md. : 1950)|February 15, 2019
Differential Influence of IL-9 and IL-17 on Actin Cytoskeleton Regulates the Migration Potential of Human KeratinocytesSreya Das, Srisathya Srinivasan, Ankita Srivastava, et al.
European Journal of Human Genetics : EJHG|June 2, 2011
17p13.3 microduplications are associated with split-hand/foot malformation and long-bone deficiency (SHFLD)Christine M Armour, Dennis E Bulman, Olga Jarinova, et al.
Molecular Cancer Research : MCR|January 31, 2020
The Th9 Axis Reduces the Oxidative Stress and Promotes the Survival of Malignant T Cells in Cutaneous T-Cell Lymphoma PatientsSushant Kumar, Bhavuk Dhamija, Soumitra Marathe, et al.
Journal of Medical Genetics|June 3, 2015
Microdeletions on 6p22.3 are associated with mesomelic dysplasia Savarirayan typeRicarda Flöttmann, Johannes Wagner, Karolina Kobus, et al.
European Journal of Human Genetics : EJHG|August 16, 2012
Prevalence of SHANK3 variants in patients with different subtypes of autism spectrum disordersLuigi Boccuto, Maria Lauri, Sara M Sarasua, et al.
Pageof 4