103 results on '"Tachdjian, Gerard"'
Search Results
2. KDM1A genotyping and expression in 146 sporadic somatotroph pituitary adenomas
3. Disrupted filamin A/αIIbβ3 interaction induces macrothrombocytopenia by increasing RhoA activity
4. Stepwise GATA1 and SMC3 mutations alter megakaryocyte differentiation in a Down syndrome leukemia model
5. OR17-05 Lysine Demethylase KDM1A And Ectopic Expression Of GIP-Receptor In Somatotropinomas Of Patients With Paradoxical Response To Oral Glucose
6. Transplantation of Human Embryonic Stem Cell–Derived Cardiovascular Progenitors for Severe Ischemic Left Ventricular Dysfunction
7. Lysine demethylase KDM1A and ectopic expression of GIP-receptor in somatotropinomas of patients with paradoxical response to oral glucose
8. A case of germline mosaicism for a 7q32.1q33 deletion in a sperm donor: consequences on pregnancy follow-up and recommendations
9. Complex translocation t(1;12;14)(q42;q14;q32) and HMGA2 deletion in a fetus presenting growth delay and bilateral cataracts
10. Inherited 1q21.1q21.2 duplication and 16p11.2 deletion: A two-hit case with more severe clinical manifestations
11. Level of RUNX1 activity is critical for leukemic predisposition but not for thrombocytopenia
12. OR04-4 Loss of KDM1A in Bilateral Macronodular Adrenal Hyperplasia With GIP-Dependent Cushing's Syndrome and in Acromegaly With Paradoxical GH Response to Oral Glucose
13. Abstract 14798: Human Embryonic Stem Cell-derived Cardiac Progenitors for Heart Failure. One-year Results of the ESCORT Trial
14. Loss of lysine demethylase KDM1A in GIP-dependent bilateral macronodular adrenal hyperplasia with Cushing's syndrome
15. Risk of tumorigenicity in mesenchymal stromal cell–based therapies—Bridging scientific observations and regulatory viewpoints
16. OR04-4 Loss of KDM1A in Bilateral Macronodular Adrenal Hyperplasia With GIP-Dependent Cushing's Syndrome and in Acromegaly With Paradoxical GH Response to Oral Glucose
17. OR04-4 Loss of KDM1A in Bilateral Macronodular Adrenal Hyperplasia With GIP-Dependent Cushing's Syndrome and in Acromegaly With Paradoxical GH Response to Oral Glucose
18. Generation of human induced pluripotent stem cell lines from five patients with Myofibrillar myopathy carrying different heterozygous mutations in the DES gene
19. Genotype–phenotype correlation in 13q13.3–q21.3 deletion
20. Preimplantation genetic diagnosis: State of the art
21. An early onset benign myopathy with glycogen storage caused by a de novo 1.4 Mb-deletion of chromosome 14
22. Coelomic fluid analysis: the absolute necessity to prove its fetal origin
23. Impact of early cleaved zygote morphology on embryo development and in vitro fertilization–embryo transfer outcome: a prospective study
24. Adequate ovarian follicular status does not prevent the decrease in pregnancy rates associated with high sperm DNA fragmentation
25. Functional variabilities of different stem cell-derived cardiomyocytes affected by several desmin mutations
26. Five years’ experience of preimplantation genetic diagnosis in the Parisian Center: outcome of the first 441 started cycles
27. SEMA3A deletion in a family with Kallmann syndrome validates the role of semaphorin 3A in human puberty and olfactory system development
28. Improvement of IVF results and optimisation of quality control by using intermittent activity
29. 15q24.1 BP4-BP1 microdeletion unmasking paternally inherited functional polymorphisms combined with distal 15q24.2q24.3 duplication in a patient with epilepsy, psychomotor delay, overweight, ventricular arrhythmia
30. First prenatal case of proximal 19p13.12 microdeletion syndrome: New insights and new delineation of the syndrome
31. First prenatal case of Kagami-Ogata syndrome associated with a small supernumerary marker chromosome derived from chromosome 15
32. Le diagnostic génétique préimplantatoire: premier bilan du groupe parisien
33. Prenatal diagnosis of isochromosome 20q in a fetus with vertebral anomaly and rocker-bottom feet
34. De novo complex intra chromosomal rearrangement after ICSI: characterisation by BACs micro array-CGH
35. Cytogenetic analysis from DNA by comparative genomic hybridization
36. Superoxide dismutase 2 (SOD2) contributes to genetic stability of native and T315I-mutated BCR-ABL expressing leukemic cells
37. Modeling Acute Megakaryoblastic Leukemia of Down Syndrome Using Induced Pluripotent Stem Cells
38. Shortening gametes co-incubation time improves live birth rate for couples with a history of fragmented embryos
39. Adrenal GIPR expression and chromosome 19q13 microduplications in GIP-dependent Cushing's syndrome
40. Small supernumerary marker chromosomes derived from chromosomes 6 and 20 in a woman with recurrent spontaneous abortions
41. Anophthalmia, hearing loss, abnormal pituitary development and response to growth hormone therapy in three children with microdeletions of 14q22q23
42. Modeling the influence of stromal microenvironment in the selection of ENU-induced BCR-ABL1 mutants by tyrosine kinase inhibitors
43. Superoxide Dismutase 2 (Sod2) Expression Is Highly Decreased In Chronic Myeloid Leukemia (CML): Contribution To Genetic Instability In Bcr-Abl-Expressing Leukemic Cells
44. A Single Chronic Myeloid Leukemia (CML) Stem Cell Harboring Both BCR-ABL and JAK2-V617F Mutation Modeled by Induced Pluripotency
45. MODELING GENETIC Diseases through Reprogramming of HUMAN Amniotic Liquid Derived CELLS
46. De novo complex intra chromosomal rearrangement after ICSI: characterisation by BACs micro array-CGH
47. Human embryonic stem cells reveal recurrent genomic instability at 20q11.21
48. Fear of Pregnancy Loss and Fetal Karyotyping: A Place for Third-Trimester Amniocentesis?
49. In Vitro Fertilization and Embryo Transfer in Seminatural Cycles for Patients With Ovarian Aging
50. In vitro fertilization and embryo transfer in seminatural cycles for patients with ovarian aging
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