Search

Your search keyword '"Department of Genetic Medicine and Development [Geneva]"' showing total 52 results

Search Constraints

Start Over You searched for: Author "Department of Genetic Medicine and Development [Geneva]" Remove constraint Author: "Department of Genetic Medicine and Development [Geneva]"
52 results on '"Department of Genetic Medicine and Development [Geneva]"'

Search Results

1. Ultrafast pulse shaping modulates perceived visual brightness in living animals

2. Sawfly Genomes Reveal Evolutionary Acquisitions That Fostered the Mega-Radiation of Parasitoid and Eusocial Hymenoptera

3. Brown marmorated stink bug, Halyomorpha halys (Stål), genome: putative underpinnings of polyphagy, insecticide resistance potential and biology of a top worldwide pest

4. Retinoic acid synthesis by ALDH1A proteins is dispensable for meiosis initiation in the mouse fetal ovary

5. Human model of IRX5 mutations reveals key role for this transcription factor in ventricular conduction

6. Molecular evolutionary trends and feeding ecology diversification in the Hemiptera, anchored by the milkweed bug genome

7. Accurate, scalable and integrative haplotype estimation

8. NRG1 signalling regulates the establishment of Sertoli cell stock in the mouse testis

9. The ReproGenomics Viewer: a multi-omics and cross-species resource compatible with single-cell studies for the reproductive science community

10. Mutations in CFAP43 and CFAP44 cause male infertility and flagellum defects in $Trypanosoma$ and human

11. Research Resource: The Dynamic Transcriptional Profile of Sertoli Cells During the Progression of Spermatogenesis

12. LKB1 and AMPKα1 are required in pancreatic alpha cells for the normal regulation of glucagon secretion and responses to hypoglycemia

13. An integrated expression atlas of miRNAs and their promoters in human and mouse

14. SPINK2 deficiency causes infertility by inducing sperm defects in heterozygotes and azoospermia inhomozygotes

15. X-linked primary ciliary dyskinesia due to mutations in the cytoplasmic axonemal dynein assembly factor PIH1D3

16. An essential role for insulin and IGF1 receptors in regulating Sertoli cells proliferation, testis size and FSH action in mice

17. HGVS Recommendations for the Description of Sequence Variants: 2016 Update

18. Systematic review of outcome domains and instruments used in clinical trials of tinnitus treatments in adults

19. Tmprss3, a Transmembrane Serine Protease Deficient in Human DFNB8/10 Deafness, Is Critical for Cochlear Hair Cell Survival at the Onset of Hearing

20. DICER Regulates the Formation and Maintenance of Cell-Cell Junctions in the Mouse Seminiferous Epithelium

21. 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

22. C2orf62 and TTC17 Are Involved in Actin Organization and Ciliogenesis in Zebrafish and Human

23. Loss of Dicer in Sertoli cells has a major impact on the testicular proteome of mice

24. A high-resolution anatomical atlas of the transcriptome in the mouse embryo

25. An Isotope-Coded Protein Labelling (ICPL) approach to assess critical roles for microRNAs in mouse spermatogenesis

26. Sertoli cell Dicer is essential for spermatogenesis in mice

27. Genome-Wide Epigenomic Analyses in Patients With Nociceptive and Neuropathic Chronic Pain Subtypes Reveals Alterations in Methylation of Genes Involved in the Neuro-Musculoskeletal System.

28. Generation of three human induced pluripotent stem cell lines with IRX5 knockout and knockin genetic editions using CRISPR-Cas9 system.

29. Human model of IRX5 mutations reveals key role for this transcription factor in ventricular conduction.

30. Gestational trophoblastic disease in Switzerland: retrospective study of the impact of a regional reference centre.

31. Hepatocellular type II fibrinogen inclusions in a patient with severe COVID-19 and hepatitis.

32. Altered BDNF Methylation in Patients with Chronic Musculoskeletal Pain and High Biopsychosocial Complexity.

33. Genetic resistance to DEHP-induced transgenerational endocrine disruption.

34. Rare single gene disorders: estimating baseline prevalence and outcomes worldwide.

35. ASSESSMENT OF KNOWLEDGE, ATTITUDE AND PRACTICE TOWARDS CONSANGUINEOUS MARRIAGES AMONG A COHORT OF MULTIETHNIC HEALTH CARE PROVIDERS IN SAUDI ARABIA.

36. Assessment of copy number variations in 120 patients with Poland syndrome.

37. Glucose-Dependent Insulinotropic Peptide Stimulates Glucagon-Like Peptide 1 Production by Pancreatic Islets via Interleukin 6, Produced by α Cells.

38. Loss of Iroquois homeobox transcription factors 3 and 5 in osteoblasts disrupts cranial mineralization.

39. HIV-1 Nef promotes infection by excluding SERINC5 from virion incorporation.

40. Prenatal Exposure to DEHP Affects Spermatogenesis and Sperm DNA Methylation in a Strain-Dependent Manner.

41. Katanin p80 regulates human cortical development by limiting centriole and cilia number.

42. Fractalkine (CX3CL1), a new factor protecting β-cells against TNFα.

43. The ethnic distribution of sickle cell disease in Sudan.

44. Consanguineous marriages : Preconception consultation in primary health care settings.

45. Homozygous deletion of a gene-free region of 4p15 in a child with multiple anomalies: could biallelic loss of conserved, non-coding elements lead to a phenotype?

46. Superovulation in mice alters the methylation pattern of imprinted genes in the sperm of the offspring.

47. Evolutionary appearance of mononucleotide repeats in the coding sequences of four genes in primates.

50. Quantification of insect genome divergence.

Catalog

Books, media, physical & digital resources