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Edwina Popek

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

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American Journal of Medical Genetics. Part A|July 5, 2016
Phenotypic expansion of TBX4 mutations to include acinar dysplasia of the lungsPrzemyslaw Szafranski, Zeynep H Coban-Akdemir, Rosemarie Rupps, et al.
Clinical Genetics|July 17, 2019
Heterozygous CTNNB1 and TBX4 variants in a patient with abnormal lung growth, pulmonary hypertension, microcephaly, and spasticityJustyna A Karolak, Przemyslaw Szafranski, David Kilner, et al.
Blood|October 27, 2005
Immunotherapy of high-risk acute leukemia with a recipient (autologous) vaccine expressing transgenic human CD40L and IL-2 after chemotherapy and allogeneic stem cell transplantationRaphaël F Rousseau, Ettore Biagi, Aurélie Dutour, et al.
Blood|October 31, 2002
Local and systemic effects of an allogeneic tumor cell vaccine combining transgenic human lymphotactin with interleukin-2 in patients with advanced or refractory neuroblastomaRaphaël F Rousseau, Ann E Haight, Charlotte Hirschmann-Jax, et al.
Human Genetics|November 6, 2019
Association of rare non-coding SNVs in the lung-specific FOXF1 enhancer with a mitigation of the lethal ACDMPV phenotypePrzemyslaw Szafranski, Qian Liu, Justyna A Karolak, et al.
The Journal of Molecular Diagnostics : JMD|February 10, 2020
Highly Sensitive Blocker Displacement Amplification and Droplet Digital PCR Reveal Low-Level Parental FOXF1 Somatic Mosaicism in Families with Alveolar Capillary Dysplasia with Misalignment of Pulmonary VeinsJustyna A Karolak, Qian Liu, Nina G Xie, et al.
Fetal Diagnosis and Therapy|June 26, 2017
Outcome and Treatment of Antenatally Diagnosed Nonimmune Hydrops FetalisAhmed A Nassr, Amen Ness, Pardis Hosseinzadeh, et al.
Human Mutation|August 8, 2018
LINE- and Alu-containing genomic instability hotspot at 16q24.1 associated with recurrent and nonrecurrent CNV deletions causative for ACDMPVPrzemyslaw Szafranski, Ewelina Kośmider, Qian Liu, et al.
American Journal of Human Genetics|January 15, 2019
Complex Compound Inheritance of Lethal Lung Developmental Disorders Due to Disruption of the TBX-FGF PathwayJustyna A Karolak, Marie Vincent, Gail Deutsch, et al.
Human Genetics|April 14, 2016
Pathogenetics of alveolar capillary dysplasia with misalignment of pulmonary veinsPrzemyslaw Szafranski, Tomasz Gambin, Avinash V Dharmadhikari, et al.
Pageof 3

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

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 30 results.
American Journal of Medical Genetics. Part A|July 5, 2016
Phenotypic expansion of TBX4 mutations to include acinar dysplasia of the lungsPrzemyslaw Szafranski, Zeynep H Coban-Akdemir, Rosemarie Rupps, et al.
Clinical Genetics|July 17, 2019
Heterozygous CTNNB1 and TBX4 variants in a patient with abnormal lung growth, pulmonary hypertension, microcephaly, and spasticityJustyna A Karolak, Przemyslaw Szafranski, David Kilner, et al.
Blood|October 27, 2005
Immunotherapy of high-risk acute leukemia with a recipient (autologous) vaccine expressing transgenic human CD40L and IL-2 after chemotherapy and allogeneic stem cell transplantationRaphaël F Rousseau, Ettore Biagi, Aurélie Dutour, et al.
Blood|October 31, 2002
Local and systemic effects of an allogeneic tumor cell vaccine combining transgenic human lymphotactin with interleukin-2 in patients with advanced or refractory neuroblastomaRaphaël F Rousseau, Ann E Haight, Charlotte Hirschmann-Jax, et al.
Human Genetics|November 6, 2019
Association of rare non-coding SNVs in the lung-specific FOXF1 enhancer with a mitigation of the lethal ACDMPV phenotypePrzemyslaw Szafranski, Qian Liu, Justyna A Karolak, et al.
The Journal of Molecular Diagnostics : JMD|February 10, 2020
Highly Sensitive Blocker Displacement Amplification and Droplet Digital PCR Reveal Low-Level Parental FOXF1 Somatic Mosaicism in Families with Alveolar Capillary Dysplasia with Misalignment of Pulmonary VeinsJustyna A Karolak, Qian Liu, Nina G Xie, et al.
Fetal Diagnosis and Therapy|June 26, 2017
Outcome and Treatment of Antenatally Diagnosed Nonimmune Hydrops FetalisAhmed A Nassr, Amen Ness, Pardis Hosseinzadeh, et al.
Human Mutation|August 8, 2018
LINE- and Alu-containing genomic instability hotspot at 16q24.1 associated with recurrent and nonrecurrent CNV deletions causative for ACDMPVPrzemyslaw Szafranski, Ewelina Kośmider, Qian Liu, et al.
American Journal of Human Genetics|January 15, 2019
Complex Compound Inheritance of Lethal Lung Developmental Disorders Due to Disruption of the TBX-FGF PathwayJustyna A Karolak, Marie Vincent, Gail Deutsch, et al.
Human Genetics|April 14, 2016
Pathogenetics of alveolar capillary dysplasia with misalignment of pulmonary veinsPrzemyslaw Szafranski, Tomasz Gambin, Avinash V Dharmadhikari, et al.
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