144 results on '"Röpke, Albrecht"'
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2. Cytogenetic and Molecular Genetic Diagnostics
3. Strukturelle Chromosomenveränderungen
4. Zyto- und molekulargenetische Untersuchungen
5. Genetic Architecture of Azoospermia—Time to Advance the Standard of Care
6. Severe, very early onset preeclampsia in a Covid 19-positive woman with a twin pregnancy presenting with a hydatidiform mole and coexisting normal fetus: a case report
7. Zyto- und molekulargenetische Untersuchungen
8. The human RHOX gene cluster: target genes and functional analysis of gene variants in infertile men.
9. Human fertilization in vivo and in vitro requires the CatSper channel to initiate sperm hyperactivation
10. Extrinsic immune cell-derived, but not intrinsic oligodendroglial factors contribute to oligodendroglial differentiation block in multiple sclerosis
11. Initial experience with [18F]DPA-714 TSPO-PET to image inflammation in primary angiitis of the central nervous system
12. X-Linked TEX11 Mutations, Meiotic Arrest, and Azoospermia in Infertile Men
13. Action of steroids and plant triterpenoids on CatSper Ca 2+ channels in human sperm
14. Genetics of Male Infertility
15. The first versatile human iPSC-based model of ectopic virus induction allows new insights in RNA-virus disease
16. Disorders of spermatogenesis: Perspectives for novel genetic diagnostics after 20 years of unchanged routine
17. WWC2 expression in the testis: Implications for spermatogenesis and male fertility
18. Intrafamilial phenotypic variability of Specific Language Impairment
19. Congenital Limb Defects: A Retrospective Cohort Study and Overview of the Literature.
20. A no-stop mutation in MAGEB4 is a possible cause of rare X-linked azoospermia and oligozoospermia in a consanguineous Turkish family
21. Congenital Limb Defects: A Retrospective Cohort Study and Overview of the Literature
22. Genetics of Male Infertility
23. Generation of a human iPSC line (MPIi008-A) from a patient with Denys-Drash syndrome
24. Translokationstrisomie 21 mit Isochromosom: unerwartete Diagnose bei atypischen sonografischen Befunden und unauffälligem NIPT
25. Azoospermia and ring chromosome 9—a case report
26. Generation of a human iPSC line (MPIi007-A) from a patient with Metachromatic leukodystrophy
27. Reprogramming competence of OCT factors is determined by transactivation domains
28. The Ca2+ channel CatSper is not activated by cAMP/PKA signaling but directly affected by chemicals used to probe the action of cAMP and PKA
29. Bi-allelic Mutations in M1AP Are a Frequent Cause of Meiotic Arrest and Severely Impaired Spermatogenesis Leading to Male Infertility
30. Generation of a human iPSC line (MPIi006-A) from a patient with Pelizaeus-Merzbacher disease
31. Crisponi syndrome/cold-induced sweating syndrome type 2: Reprogramming of CS/CISS2 individual derived fibroblasts into three clones of one iPSC line
32. Generation of induced pluripotent stem cell lines from a Crisponi/Cold induced sweating syndrome type 1 individual
33. Shedding light on the control of CatSper Ca2+channels by cAMP and chemicals used to probe cAMP signaling
34. Rotational motion and rheotaxis of human sperm do not require functional CatSper channels and transmembrane Ca 2+ signaling
35. Cardiac Subtype-Specific Modeling of Kv1.5 Ion Channel Deficiency Using Human Pluripotent Stem Cells
36. Rotational motion and rheotaxis of human sperm do not require functional CatSper channels and transmembrane Ca2+ signaling.
37. Disorders of spermatogenesis
38. Cardiogenic programming of human pluripotent stem cells by dose-controlled activation of EOMES
39. MECHANISMS IN ENDOCRINOLOGY: Aberrations of the X chromosome as cause of male infertility
40. Generation and cardiac subtype-specific differentiation of PITX2-deficient human iPS cell lines for exploring familial atrial fibrillation
41. Astrocyte pathology in a human neural stem cell model of frontotemporal dementia caused by mutant TAU protein
42. The humanRHOXgene cluster: target genes and functional analysis of gene variants in infertile men
43. Aberrations of the X chromosome as cause of male infertility.
44. Distinct Neurodegenerative Changes in an Induced Pluripotent Stem Cell Model of Frontotemporal Dementia Linked to Mutant TAU Protein
45. Universal Cardiac Induction of Human Pluripotent Stem Cells in Two and Three-Dimensional Formats: Implications for In Vitro Maturation
46. Genetic Variants of DICE1/INTS6 in German Prostate Cancer Families with Linkage to 13q14
47. Azoospermia and ring chromosome 9—a case report
48. Cardiac Subtype-Specific Modeling of Kv1.5 Ion Channel Deficiency Using Human Pluripotent Stem Cells.
49. Action of steroids and plant triterpenoids on CatSper Ca2+ channels in human sperm.
50. The Ca2+channel CatSper is not activated by cAMP/PKA signaling but directly affected by chemicals used to probe the action of cAMP and PKA.
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