130 results on '"Jaruzelska, Jadwiga"'
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2. RNAlign2D: a rapid method for combined RNA structure and sequence-based alignment using a pseudo-amino acid substitution matrix
3. PUM1 and PUM2 exhibit different modes of regulation for SIAH1 that involve cooperativity with NANOS paralogues
4. Human Pumilio-2 Is Expressed in Embryonic Stem Cells and Germ Cells and Interacts with DAZ (Deleted in AZoospermia) and DAZ-Like Proteins
5. Emerging Roles of NANOS RNA-Binding Proteins in Cancer
6. Distinct Roles of NANOS1 and NANOS3 in the Cell Cycle and NANOS3-PUM1-FOXM1 Axis to Control G2/M Phase in a Human Primordial Germ Cell Model
7. A Novel WT1 Mutation Identified in a 46,XX Testicular/Ovotesticular DSD Patient Results in the Retention of Intron 9
8. Additional file 1 of RNAlign2D: a rapid method for combined RNA structure and sequence-based alignment using a pseudo-amino acid substitution matrix
9. NANOS1 and PUMILIO2 bind microRNA biogenesis factor GEMIN3, within chromatoid body in human germ cells
10. The FKBP4 gene, encoding a regulator of the androgen receptor signaling pathway, is a novel candidate gene for androgen insensitivity syndrome
11. Role of PUM RNA-Binding Proteins in Cancer
12. Conservation of a Pumilio-Nanos complex from Drosophila germ plasm to human germ cells
13. Mutations of NANOS1, a human homologue of the Drosophila morphogen, are associated with a lack of germ cells in testes or severe oligo-astheno-teratozoospermia
14. The FKBP4 Gene, Encoding a Regulator of the Androgen Receptor Signaling Pathway, Is a Novel Candidate Gene for Androgen Insensitivity Syndrome
15. RNAlign2D – a rapid method for combined RNA structure and sequence-based alignment using a pseudo-amino acid substitution matrix
16. Human NANOS1 Represses Apoptosis by Downregulating Pro-Apoptotic Genes in the Male Germ Cell Line
17. Characterization of RNP Networks of PUM1 and PUM2 Post-Transcriptional Regulators in TCam-2 Cells, a Human Male Germ Cell Model
18. The gene encoding the ketogenic enzyme HMGCS2 displays a unique expression during gonad development in mice
19. Kinesin KIF18A is a novel PUM regulated target promoting mitotic progression and survival of human male germ cell line
20. The codon 408 mutation associated with haplotype 2 is predominant in Polish families with phenylketonuria
21. Mosaicism for 45,X cell line may accentuate the severity of spermatogenic defects in men with AZFc deletion
22. Incomplete masculinisation of XX subjects carrying the SRY gene on an inactive X chromosome
23. A Case of Two Sisters Suffering from 46,XY Gonadal Dysgenesis and Carrying a Mutation of a Novel Candidate Sex-Determining Gene STARD8 on the X Chromosome
24. A male infertility mutation reverts NANOS1 activity from anti-apoptotic to pro-apoptotic by disrupting repression ofGADD45A,GADD45B,GADD45GandRHOBgenes
25. Kinesin KIF18A is a novel PUM regulated target promoting mitotic progression and survival of human male germ cell line - TCam-2
26. T-psi-C: user friendly database of tRNA sequences and structures
27. Human PUM1 and PUM2 exhibit regulation of divergent mRNA targets in male germ cells
28. The phenylketonuria G272X haplotype 7 mutation in European populations
29. Deletion mapping of interval 6 of the human Y chromosome
30. Human Y-chromosome variation in the Western Mediterranean area: implications for the peopling of the region
31. Kinesin KIF18A is a novel PUM-regulated target promoting mitotic progression and survival of a human male germ cell line.
32. T-psi-C: user friendly database of tRNA sequences and structures.
33. PUM1 and PUM2 exhibit different modes of regulation for SIAH1 that involve cooperativity with NANOS paralogues
34. SPIN1 is a proto-oncogene and SPIN3 is a tumor suppressor in human seminoma
35. Small nuclear RNAs synthesis in PHA-stimulated and nonstimulated human peripheral blood lymphocytes
36. A Case of Wiedemann-Steiner Syndrome Associated with a 46,XY Disorder of Sexual Development and Gonadal Dysgenesis
37. Loss of Function Mutation in the Palmitoyl-Transferase HHAT Leads to Syndromic 46,XY Disorder of Sex Development by Impeding Hedgehog Protein Palmitoylation and Signaling
38. Mutations ofNANOS1, a human homologue of theDrosophilamorphogen, are associated with a lack of germ cells in testes or severe oligo-astheno-teratozoospermia
39. A Case of Wiedemann-Steiner Syndrome Associated with a 46,XY Disorder of Sexual Development and Gonadal Dysgenesis.
40. NANOS3 gene mutations in men with isolated sterility phenotype
41. A simplified method for detection of the mutations predominantly causing cystic fibrosis and phenylketonuria in Polish families
42. Identification of a novel gene, DZIP (DAZ-interacting protein), that encodes a protein that interacts with DAZ (deleted in azoospermia) and is expressed in embryonic stem cells and germ cells
43. Spatial and temporal distribution of the neutral polymorphisms in the last ZFX intron: analysis of the haplotype structure and genealogy
44. In Vitro Splicing Deficiency Induced by a C to T Mutation at Position −3 in the Intron 10 Acceptor Site of the Phenylalanine Hydroxylase Gene in a Patient with Phenylketonuria
45. A region of human chromosome 9p required for testis development contains two genes related to known sexual regulators.
46. In VitroSplicing Deficiency Induced by a C to T Mutation at Position −3 in the Intron 10 Acceptor Site of the Phenylalanine Hydroxylase Gene in a Patient with Phenylketonuria(∗)
47. Candidate mRNAs interacting with fertility protein PUMILIO2 in the human germ line
48. Human fertility protein PUMILIO2 interacts in vitro with testis mRNA encoding Cdc42 effector 3 (CEP3)
49. The FKBP4 gene, encoding a regulator of the androgen receptor signaling pathway, is a novel candidate gene for androgen insensitivity syndrome
50. A simplified method for detection of the mutations predominantly causing cystic fibrosis and phenylketonuria in Polish families.
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