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1

Genotype-phenotype correlations in cystic fibrosis حسب Eitan Kerem, Batsheva Kerem

منشور في 1996

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Revisão

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2

Molecular Pharmacology of the Sodium Channel Mutation D1790G Linked to the Long-QT Syndrome حسب Hugues Abriel, Xander H.T. Wehrens, Jesaia Benhorin, Batsheva Kerem, Robert S. Kass

منشور في 2000

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Artigo

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3

The efficiency of nonsense-mediated mRNA decay is an inherent character and varies among different cells حسب Liat Linde, Stephanie Boelz, Gabriele Neu‐Yilik, Andreas E. Kulozik, Batsheva Kerem

منشور في 2007

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Artigo

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4

Oncogenes create a unique landscape of fragile sites حسب Karin Miron, Tamar Golan‐Lev, Raz Dvir, Eyal Ben‐David, Batsheva Kerem

منشور في 2015

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Artigo

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محفوظ في:
5

Gene, RNA, and ASO-based therapeutic approaches in Cystic Fibrosis حسب Norm Allaire, Uta Griesenbach, Batsheva Kerem, John D. Lueck, Noemie Stanleigh, Yifat S. Oren

منشور في 2023

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Artigo

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6

Failure of Origin Activation in Response to Fork Stalling Leads to Chromosomal Instability at Fragile Sites حسب E. Ozeri-Galai, Ronald Lebofsky, Ayelet Rahat, Assaf C. Bester, Aaron Bensimon, Batsheva Kerem

منشور في 2011

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Artigo

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7

Replication Delay along FRA7H, a Common Fragile Site on Human Chromosome 7, Leads to Chromosomal Instability حسب Asaf Hellman, Ayelet Rahat, Stephen W. Scherer, Ariel Darvasi, Lap‐Chee Tsui, Batsheva Kerem

منشور في 2000

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Artigo

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8

Genomic Instability in Human Pluripotent Stem Cells Arises from Replicative Stress and Chromosome Condensation Defects حسب Noa Lamm, Uri Ben‐David, Tamar Golan‐Lev, Zuzana Štorchová, Nissim Benvenisty, Batsheva Kerem

منشور في 2015

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Artigo

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9

Novel LQT-3 Mutation Affects Na + Channel Activity Through Interactions Between α- and β 1 -Subunits حسب Rui-Hai An, X. L. Wang, Batsheva Kerem, Jesaia Benhorin, Aharon Medina, Maya Goldmit, Robert S. Kass

منشور في 1998

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Artigo

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10

AT-dinucleotide rich sequences drive fragile site formation حسب Michal Irony‐Tur Sinai, Anita Salamon, Noemie Stanleigh, Tchelet Goldberg, Aryeh Weiss, Yuh‐Hwa Wang, Batsheva Kerem

منشور في 2019

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Artigo

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11

New approaches to genetic therapies for cystic fibrosis حسب A. Christopher Boyd, Shuling Guo, Lulu Huang, Batsheva Kerem, Yifat S. Oren, Amy J. Walker, Stephen L. Hart

منشور في 2020

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Revisão

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12

A role for common fragile site induction in amplification of human oncogenes حسب Asaf Hellman, Eitan Zlotorynski, Stephen W. Scherer, Joseph Cheung, John B. Vincent, Jeremy C. Smith, Luba Trakhtenbrot, Batsheva Kerem

منشور في 2002

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Artigo

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13

The Relation between Genotype and Phenotype in Cystic Fibrosis — Analysis of the Most Common Mutation (ΔF508) حسب Eitan Kerem, Mary Corey, Batsheva Kerem, Johanna M. Rommens, D. Markiewicz, Henry Levison, Lap‐Chee Tsui, Peter R. Durie

منشور في 1990

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Artigo

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14

The presence of extra chromosomes leads to genomic instability حسب Verena Passerini, E. Ozeri-Galai, Mirjam S. de Pagter, Neysan Donnelly, Sarah Schmalbrock, Wigard P. Kloosterman, Batsheva Kerem, Zuzana Štorchová

منشور في 2016

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Artigo

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15

Identification of mutations in regions corresponding to the two putative nucleotide (ATP)-binding folds of the cystic fibrosis gene. حسب Batsheva Kerem, Julian Zielenski, D. Markiewicz, Dominique Bozon, Ephraim Gazit, Jacob Yahav, Derek Kennedy, J.R. Riordan, Francis S. Collins, Johanna M. Rommens

منشور في 1990

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Artigo

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16

Molecular Basis for Expression of Common and Rare Fragile Sites حسب Eitan Zlotorynski, Ayelet Rahat, Jennifer Skaug, N Ben-Porat, Efrat Ozeri, Ruth Hershberg, Ayala Levi, Stephen W. Scherer, Hanah Margalit, Batsheva Kerem

منشور في 2003

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Artigo

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17

Nucleotide Deficiency Promotes Genomic Instability in Early Stages of Cancer Development حسب Assaf C. Bester, Maayan Roniger, Yifat S. Oren, Michael M. Im, Dan Sarni, Malka Chaoat, Aaron Bensimon, Gideon Zamir, Donna S. Shewach, Batsheva Kerem

منشور في 2011

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Artigo

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18

3D genome organization contributes to genome instability at fragile sites حسب Dan Sarni, Takayo Sasaki, Michal Irony Tur-Sinai, Karin Miron, Juan Carlos Rivera‐Mulia, Brian Magnuson, Mats Ljungman, David M. Gilbert, Batsheva Kerem

منشور في 2020

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Artigo

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19

Homologous recombination and nonhomologous end-joining repair pathways regulate fragile site stability حسب Michal Schwartz, Eitan Zlotorynski, Michal Goldberg, Efrat Ozeri, Ayelet Rahat, Carlos le Sage, Benjamin P.C. Chen, David J. Chen, Reuven Agami, Batsheva Kerem

منشور في 2005

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Artigo

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محفوظ في:
20

Nonsense-mediated mRNA decay affects nonsense transcript levels and governs response of cystic fibrosis patients to gentamicin حسب Liat Linde, Stephanie Boelz, Malka Nissim‐Rafinia, Yifat S. Oren, Michael Wilschanski, Yasmin Yaacov, Dov Virgilis, Gabriele Neu‐Yilik, Andreas E. Kulozik, Eitan Kerem, Batsheva Kerem

منشور في 2007

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Artigo

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محفوظ في:

Genotype-phenotype correlations in cystic fibrosis حسب Eitan Kerem, Batsheva Kerem

Molecular Pharmacology of the Sodium Channel Mutation D1790G Linked to the Long-QT Syndrome حسب Hugues Abriel, Xander H.T. Wehrens, Jesaia Benhorin, Batsheva Kerem, Robert S. Kass

The efficiency of nonsense-mediated mRNA decay is an inherent character and varies among different cells حسب Liat Linde, Stephanie Boelz, Gabriele Neu‐Yilik, Andreas E. Kulozik, Batsheva Kerem

Oncogenes create a unique landscape of fragile sites حسب Karin Miron, Tamar Golan‐Lev, Raz Dvir, Eyal Ben‐David, Batsheva Kerem

Gene, RNA, and ASO-based therapeutic approaches in Cystic Fibrosis حسب Norm Allaire, Uta Griesenbach, Batsheva Kerem, John D. Lueck, Noemie Stanleigh, Yifat S. Oren

Failure of Origin Activation in Response to Fork Stalling Leads to Chromosomal Instability at Fragile Sites حسب E. Ozeri-Galai, Ronald Lebofsky, Ayelet Rahat, Assaf C. Bester, Aaron Bensimon, Batsheva Kerem

Replication Delay along FRA7H, a Common Fragile Site on Human Chromosome 7, Leads to Chromosomal Instability حسب Asaf Hellman, Ayelet Rahat, Stephen W. Scherer, Ariel Darvasi, Lap‐Chee Tsui, Batsheva Kerem

Genomic Instability in Human Pluripotent Stem Cells Arises from Replicative Stress and Chromosome Condensation Defects حسب Noa Lamm, Uri Ben‐David, Tamar Golan‐Lev, Zuzana Štorchová, Nissim Benvenisty, Batsheva Kerem

Novel LQT-3 Mutation Affects Na <sup>+</sup> Channel Activity Through Interactions Between α- and β <sub>1</sub> -Subunits حسب Rui-Hai An, X. L. Wang, Batsheva Kerem, Jesaia Benhorin, Aharon Medina, Maya Goldmit, Robert S. Kass

AT-dinucleotide rich sequences drive fragile site formation حسب Michal Irony‐Tur Sinai, Anita Salamon, Noemie Stanleigh, Tchelet Goldberg, Aryeh Weiss, Yuh‐Hwa Wang, Batsheva Kerem

New approaches to genetic therapies for cystic fibrosis حسب A. Christopher Boyd, Shuling Guo, Lulu Huang, Batsheva Kerem, Yifat S. Oren, Amy J. Walker, Stephen L. Hart

A role for common fragile site induction in amplification of human oncogenes حسب Asaf Hellman, Eitan Zlotorynski, Stephen W. Scherer, Joseph Cheung, John B. Vincent, Jeremy C. Smith, Luba Trakhtenbrot, Batsheva Kerem

The Relation between Genotype and Phenotype in Cystic Fibrosis — Analysis of the Most Common Mutation (ΔF<sub>508</sub>) حسب Eitan Kerem, Mary Corey, Batsheva Kerem, Johanna M. Rommens, D. Markiewicz, Henry Levison, Lap‐Chee Tsui, Peter R. Durie

The presence of extra chromosomes leads to genomic instability حسب Verena Passerini, E. Ozeri-Galai, Mirjam S. de Pagter, Neysan Donnelly, Sarah Schmalbrock, Wigard P. Kloosterman, Batsheva Kerem, Zuzana Štorchová

Molecular Basis for Expression of Common and Rare Fragile Sites حسب Eitan Zlotorynski, Ayelet Rahat, Jennifer Skaug, N Ben-Porat, Efrat Ozeri, Ruth Hershberg, Ayala Levi, Stephen W. Scherer, Hanah Margalit, Batsheva Kerem

Nucleotide Deficiency Promotes Genomic Instability in Early Stages of Cancer Development حسب Assaf C. Bester, Maayan Roniger, Yifat S. Oren, Michael M. Im, Dan Sarni, Malka Chaoat, Aaron Bensimon, Gideon Zamir, Donna S. Shewach, Batsheva Kerem

3D genome organization contributes to genome instability at fragile sites حسب Dan Sarni, Takayo Sasaki, Michal Irony Tur-Sinai, Karin Miron, Juan Carlos Rivera‐Mulia, Brian Magnuson, Mats Ljungman, David M. Gilbert, Batsheva Kerem

Homologous recombination and nonhomologous end-joining repair pathways regulate fragile site stability حسب Michal Schwartz, Eitan Zlotorynski, Michal Goldberg, Efrat Ozeri, Ayelet Rahat, Carlos le Sage, Benjamin P.C. Chen, David J. Chen, Reuven Agami, Batsheva Kerem

نتائج البحث - Batsheva Kerem

Genotype-phenotype correlations in cystic fibrosis حسب Eitan Kerem, Batsheva Kerem

Molecular Pharmacology of the Sodium Channel Mutation D1790G Linked to the Long-QT Syndrome حسب Hugues Abriel, Xander H.T. Wehrens, Jesaia Benhorin, Batsheva Kerem, Robert S. Kass

The efficiency of nonsense-mediated mRNA decay is an inherent character and varies among different cells حسب Liat Linde, Stephanie Boelz, Gabriele Neu‐Yilik, Andreas E. Kulozik, Batsheva Kerem

Oncogenes create a unique landscape of fragile sites حسب Karin Miron, Tamar Golan‐Lev, Raz Dvir, Eyal Ben‐David, Batsheva Kerem

Gene, RNA, and ASO-based therapeutic approaches in Cystic Fibrosis حسب Norm Allaire, Uta Griesenbach, Batsheva Kerem, John D. Lueck, Noemie Stanleigh, Yifat S. Oren

Failure of Origin Activation in Response to Fork Stalling Leads to Chromosomal Instability at Fragile Sites حسب E. Ozeri-Galai, Ronald Lebofsky, Ayelet Rahat, Assaf C. Bester, Aaron Bensimon, Batsheva Kerem

Replication Delay along FRA7H, a Common Fragile Site on Human Chromosome 7, Leads to Chromosomal Instability حسب Asaf Hellman, Ayelet Rahat, Stephen W. Scherer, Ariel Darvasi, Lap‐Chee Tsui, Batsheva Kerem

Genomic Instability in Human Pluripotent Stem Cells Arises from Replicative Stress and Chromosome Condensation Defects حسب Noa Lamm, Uri Ben‐David, Tamar Golan‐Lev, Zuzana Štorchová, Nissim Benvenisty, Batsheva Kerem

Novel LQT-3 Mutation Affects Na <sup>+</sup> Channel Activity Through Interactions Between α- and β <sub>1</sub> -Subunits حسب Rui-Hai An, X. L. Wang, Batsheva Kerem, Jesaia Benhorin, Aharon Medina, Maya Goldmit, Robert S. Kass

AT-dinucleotide rich sequences drive fragile site formation حسب Michal Irony‐Tur Sinai, Anita Salamon, Noemie Stanleigh, Tchelet Goldberg, Aryeh Weiss, Yuh‐Hwa Wang, Batsheva Kerem

New approaches to genetic therapies for cystic fibrosis حسب A. Christopher Boyd, Shuling Guo, Lulu Huang, Batsheva Kerem, Yifat S. Oren, Amy J. Walker, Stephen L. Hart

A role for common fragile site induction in amplification of human oncogenes حسب Asaf Hellman, Eitan Zlotorynski, Stephen W. Scherer, Joseph Cheung, John B. Vincent, Jeremy C. Smith, Luba Trakhtenbrot, Batsheva Kerem

The Relation between Genotype and Phenotype in Cystic Fibrosis — Analysis of the Most Common Mutation (ΔF<sub>508</sub>) حسب Eitan Kerem, Mary Corey, Batsheva Kerem, Johanna M. Rommens, D. Markiewicz, Henry Levison, Lap‐Chee Tsui, Peter R. Durie

The presence of extra chromosomes leads to genomic instability حسب Verena Passerini, E. Ozeri-Galai, Mirjam S. de Pagter, Neysan Donnelly, Sarah Schmalbrock, Wigard P. Kloosterman, Batsheva Kerem, Zuzana Štorchová

Molecular Basis for Expression of Common and Rare Fragile Sites حسب Eitan Zlotorynski, Ayelet Rahat, Jennifer Skaug, N Ben-Porat, Efrat Ozeri, Ruth Hershberg, Ayala Levi, Stephen W. Scherer, Hanah Margalit, Batsheva Kerem

Nucleotide Deficiency Promotes Genomic Instability in Early Stages of Cancer Development حسب Assaf C. Bester, Maayan Roniger, Yifat S. Oren, Michael M. Im, Dan Sarni, Malka Chaoat, Aaron Bensimon, Gideon Zamir, Donna S. Shewach, Batsheva Kerem

3D genome organization contributes to genome instability at fragile sites حسب Dan Sarni, Takayo Sasaki, Michal Irony Tur-Sinai, Karin Miron, Juan Carlos Rivera‐Mulia, Brian Magnuson, Mats Ljungman, David M. Gilbert, Batsheva Kerem

Homologous recombination and nonhomologous end-joining repair pathways regulate fragile site stability حسب Michal Schwartz, Eitan Zlotorynski, Michal Goldberg, Efrat Ozeri, Ayelet Rahat, Carlos le Sage, Benjamin P.C. Chen, David J. Chen, Reuven Agami, Batsheva Kerem

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