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G Mehta

Showing results (351-360 of 402) with videos related to

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Clinical Genetics|October 16, 2007
Novel VCP mutations in inclusion body myopathy associated with Paget disease of bone and frontotemporal dementiaG D J Watts, D Thomasova, S K Ramdeen, et al.
Planta Medica|September 11, 2002
Bioactive constituents of the seeds of Brucea javanicaBao-Ning Su, Leng Chee Chang, Eun Jung Park, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|May 31, 2017
Lessons Learned: Early Termination of a Randomized Trial of Calcineurin Inhibitor and Corticosteroid Avoidance Using BelataceptK A Newell, A K Mehta, C P Larsen, et al.
Journal of Medical Genetics|April 18, 2025
Phenotypic heterogeneity in <i>DYNC2H1</i>-related short-rib thoracic dysplasia: antenatal indicators and postnatal outcomesNikhil Pattani, Nour Elkhateeb, Aakash Joshi, et al.
Biology Open|May 6, 2020
A novel and cost-effective <i>ex vivo</i> orthotopic model for the study of human breast cancer in mouse mammary gland organ cultureAkash Gupta, Geetanjali Gupta, Rajeshwari R Mehta, et al.
Prenatal Diagnosis|June 19, 2026
Is There Potential Clinical Utility in Reporting Variants of Uncertain Significance From Prenatal Sequencing?A Gibbs, R Braham, V Ramachandran, et al.
Carcinogenesis|August 19, 2006
Inhibition of estrogen-independent mammary carcinogenesis by disruption of growth hormone signalingXiao Zhang, Rajendra G Mehta, Daniel D Lantvit, et al.
Bone Reports|July 25, 2022
<i>SMAD3</i> mutation in LDS3 causes bone fragility by impairing the TGF-β pathway and enhancing osteoclastogenesisAhmed El-Gazzar, Heeseog Kang, Nadja Fratzl-Zelman, et al.
Biochimica Et Biophysica Acta|October 29, 2013
Mutation of the human mitochondrial phenylalanine-tRNA synthetase causes infantile-onset epilepsy and cytochrome c oxidase deficiencyAbdulraheem Almalki, Charlotte L Alston, Alasdair Parker, et al.
Journal of Medical Genetics|July 16, 2016
Mutations specific to the Rac-GEF domain of <i>TRIO</i> cause intellectual disability and microcephalyReuben J Pengelly, Stephanie Greville-Heygate, Susanne Schmidt, et al.
Pageof 41

Showing results (351-360 of 402) with videos related to

Sort By:
Pageof 41
Clinical Genetics|October 16, 2007
Novel VCP mutations in inclusion body myopathy associated with Paget disease of bone and frontotemporal dementiaG D J Watts, D Thomasova, S K Ramdeen, et al.
Planta Medica|September 11, 2002
Bioactive constituents of the seeds of Brucea javanicaBao-Ning Su, Leng Chee Chang, Eun Jung Park, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|May 31, 2017
Lessons Learned: Early Termination of a Randomized Trial of Calcineurin Inhibitor and Corticosteroid Avoidance Using BelataceptK A Newell, A K Mehta, C P Larsen, et al.
Journal of Medical Genetics|April 18, 2025
Phenotypic heterogeneity in <i>DYNC2H1</i>-related short-rib thoracic dysplasia: antenatal indicators and postnatal outcomesNikhil Pattani, Nour Elkhateeb, Aakash Joshi, et al.
Biology Open|May 6, 2020
A novel and cost-effective <i>ex vivo</i> orthotopic model for the study of human breast cancer in mouse mammary gland organ cultureAkash Gupta, Geetanjali Gupta, Rajeshwari R Mehta, et al.
Prenatal Diagnosis|June 19, 2026
Is There Potential Clinical Utility in Reporting Variants of Uncertain Significance From Prenatal Sequencing?A Gibbs, R Braham, V Ramachandran, et al.
Carcinogenesis|August 19, 2006
Inhibition of estrogen-independent mammary carcinogenesis by disruption of growth hormone signalingXiao Zhang, Rajendra G Mehta, Daniel D Lantvit, et al.
Bone Reports|July 25, 2022
<i>SMAD3</i> mutation in LDS3 causes bone fragility by impairing the TGF-β pathway and enhancing osteoclastogenesisAhmed El-Gazzar, Heeseog Kang, Nadja Fratzl-Zelman, et al.
Biochimica Et Biophysica Acta|October 29, 2013
Mutation of the human mitochondrial phenylalanine-tRNA synthetase causes infantile-onset epilepsy and cytochrome c oxidase deficiencyAbdulraheem Almalki, Charlotte L Alston, Alasdair Parker, et al.
Journal of Medical Genetics|July 16, 2016
Mutations specific to the Rac-GEF domain of <i>TRIO</i> cause intellectual disability and microcephalyReuben J Pengelly, Stephanie Greville-Heygate, Susanne Schmidt, et al.
Pageof 41