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1. LARP1 haploinsufficiency is associated with an autosomal dominant neurodevelopmental disorder.

3. Comprehensive EHMT1 variants analysis broadens genotype-phenotype associations and molecular mechanisms in Kleefstra syndrome

4. Diagnostic Utility of Exome Sequencing Among Israeli Children With Kidney Failure

5. Context-dependent functional compensation between Ythdf m6A reader proteins

6. A multidisciplinary nephrogenetic referral clinic for children and adults—diagnostic achievements and insights

7. SUMOylation of linker histone H1 drives chromatin condensation and restriction of embryonic cell fate identity

8. Principles of signaling pathway modulation for enhancing human naive pluripotency induction

9. Comprehensive EHMT1 variants analysis broadens genotype-phenotype associations and molecular mechanisms in Kleefstra syndrome

10. A single center experience with publicly funded clinical exome sequencing for neurodevelopmental disorders or multiple congenital anomalies

11. Deterministic Somatic Cell Reprogramming Involves Continuous Transcriptional Changes Governed by Myc and Epigenetic-Driven Modules

12. Intellectual disability syndrome associated with a homozygous founder variant inSGSM3in Ashkenazi Jews

13. Neutralizing Gatad2a-Chd4-Mbd3/NuRD Complex Facilitates Deterministic Induction of Naive Pluripotency

15. Intellectual disability syndrome associated with a homozygous founder variant in SGSM3 in Ashkenazi Jews.

16. Intellectual disability syndrome associated with a homozygous founder variant in SGSM3in Ashkenazi Jews

17. m 6 A mRNA methylation facilitates resolution of naïve pluripotency toward differentiation

19. FC035: Exome Sequencing of the Israeli Dialysis-Treated Pediatric Population Reveals Monogenic Etiology in ∼44% of Cases

21. Myelin-associated glycoprotein gene mutation causes Pelizaeus-Merzbacher disease-like disorder

22. STEM CELLS: m6A mRNA methylation facilitates resolution of naive pluripotency toward differentiation

23. Deterministic direct reprogramming of somatic cells to pluripotency

24. Context-dependent functional compensation between Ythdf m6A readers

25. Tripartite Inhibition of SRC-WNT-PKC Signalling Consolidates Human Naïve Pluripotency

26. Corrigendum: Deterministic direct reprogramming of somatic cells to pluripotency

28. Neutralizing Gatad2a-Chd4-Mbd3 Axis within the NuRD Complex Facilitates Deterministic Induction of Naïve Pluripotency

29. The Molecular and Functional Foundations of Conducive Somatic Cell Reprogramming to Ground State Pluripotency

30. Myelin-associated glycoprotein gene mutation causes Pelizaeus-Merzbacher disease-like disorder

31. High-Resolution Dissection of Conducive Reprogramming Trajectory to Ground State Pluripotency

32. Erratum: Corrigendum: Deterministic direct reprogramming of somatic cells to pluripotency

34. Myelin-associated glycoprotein gene mutation causes Pelizaeus-Merzbacher disease-like disorder

35. m6A mRNA methylation facilitates resolution of naïve pluripotency toward differentiation.

36. Context-dependent functional compensation between Ythdf m 6 A reader proteins.

37. Characteristics of Synthetic Cannabinoid and Cannabis Users Admitted to a Psychiatric Hospital: A Comparative Study.

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