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Clinical Immunology (Orlando, Fla.)
|
June 1, 2011
Novel mutations in RAG1/2 and ADA genes in Israeli patients presenting with T-B-SCID or Omenn syndrome
Ilan Dalal, Diana Tasher, Raz Somech, et al.
Journal of Cellular Biochemistry
|
June 22, 2010
Beclin 1 self-association is independent of autophagy induction by amino acid deprivation and rapamycin treatment
Shelly Adi-Harel, Shlomit Erlich, Eran Schmukler, et al.
Journal of Clinical Pharmacology
|
July 1, 2021
Physiologically Based Pharmacokinetic Modeling for Selumetinib to Evaluate Drug-Drug Interactions and Pediatric Dose Regimens
Sarit Cohen-Rabbie, Li Zhou, Karthick Vishwanathan, et al.
Journal of Genetic Counseling
|
November 24, 2011
Genetic counseling and testing for FSHD (facioscapulohumeral muscular dystrophy) in the Israeli population
Miri Yanoov-Sharav, Esther Leshinsky-Silver, Sarit Cohen, et al.
Molecular Genetics and Metabolism
|
April 15, 2009
NDUFS4 mutations cause Leigh syndrome with predominant brainstem involvement
E Leshinsky-Silver, Anne-Sophie Lebre, Limor Minai, et al.
Cancer Chemotherapy and Pharmacology
|
April 27, 2021
Population pharmacokinetics and exposure-response of selumetinib and its N-desmethyl metabolite in pediatric patients with neurofibromatosis type 1 and inoperable plexiform neurofibromas
Stein Schalkwijk, Li Zhou, Sarit Cohen-Rabbie, et al.
European Journal of Immunology
|
February 22, 2021
Commensal fungi and their cell-wall β-glucans direct differential responses in human intestinal epithelial cells
Sarit Cohen-Kedar, Danielle Keizer, Suzana Schwartz, et al.
British Journal of Clinical Pharmacology
|
August 20, 2021
Concentration-QT modelling in early clinical oncology settings: Simulation evaluation of performance
Gael Cantet, Alienor Berges, Rhianna O'Sullivan, et al.
Scientific Reports
|
September 30, 2018
Live Cell Imaging of Bioorthogonally Labelled Proteins Generated With a Single Pyrrolysine tRNA Gene
Noa Aloush, Tomer Schvartz, Andres I König, et al.
European Journal of Human Genetics : EJHG
|
November 25, 2010
A large homozygous deletion in the SAMHD1 gene causes atypical Aicardi-Goutiéres syndrome associated with mtDNA deletions
Esther Leshinsky-Silver, Gustavo Malinger, Liat Ben-Sira, et al.
Page
of 6
Search research articles
Search
Showing results (41-50 of 59) with videos related to
Sort By:
Page
of 6
Clinical Immunology (Orlando, Fla.)
|
June 1, 2011
Novel mutations in RAG1/2 and ADA genes in Israeli patients presenting with T-B-SCID or Omenn syndrome
Ilan Dalal, Diana Tasher, Raz Somech, et al.
Journal of Cellular Biochemistry
|
June 22, 2010
Beclin 1 self-association is independent of autophagy induction by amino acid deprivation and rapamycin treatment
Shelly Adi-Harel, Shlomit Erlich, Eran Schmukler, et al.
Journal of Clinical Pharmacology
|
July 1, 2021
Physiologically Based Pharmacokinetic Modeling for Selumetinib to Evaluate Drug-Drug Interactions and Pediatric Dose Regimens
Sarit Cohen-Rabbie, Li Zhou, Karthick Vishwanathan, et al.
Journal of Genetic Counseling
|
November 24, 2011
Genetic counseling and testing for FSHD (facioscapulohumeral muscular dystrophy) in the Israeli population
Miri Yanoov-Sharav, Esther Leshinsky-Silver, Sarit Cohen, et al.
Molecular Genetics and Metabolism
|
April 15, 2009
NDUFS4 mutations cause Leigh syndrome with predominant brainstem involvement
E Leshinsky-Silver, Anne-Sophie Lebre, Limor Minai, et al.
Cancer Chemotherapy and Pharmacology
|
April 27, 2021
Population pharmacokinetics and exposure-response of selumetinib and its N-desmethyl metabolite in pediatric patients with neurofibromatosis type 1 and inoperable plexiform neurofibromas
Stein Schalkwijk, Li Zhou, Sarit Cohen-Rabbie, et al.
European Journal of Immunology
|
February 22, 2021
Commensal fungi and their cell-wall β-glucans direct differential responses in human intestinal epithelial cells
Sarit Cohen-Kedar, Danielle Keizer, Suzana Schwartz, et al.
British Journal of Clinical Pharmacology
|
August 20, 2021
Concentration-QT modelling in early clinical oncology settings: Simulation evaluation of performance
Gael Cantet, Alienor Berges, Rhianna O'Sullivan, et al.
Scientific Reports
|
September 30, 2018
Live Cell Imaging of Bioorthogonally Labelled Proteins Generated With a Single Pyrrolysine tRNA Gene
Noa Aloush, Tomer Schvartz, Andres I König, et al.
European Journal of Human Genetics : EJHG
|
November 25, 2010
A large homozygous deletion in the SAMHD1 gene causes atypical Aicardi-Goutiéres syndrome associated with mtDNA deletions
Esther Leshinsky-Silver, Gustavo Malinger, Liat Ben-Sira, et al.
Page
of 6