Tachdjian, Gérard
Gérard Tachdjian médecin français
VIAF ID: 42076980 (Personal)
Permalink: http://viaf.org/viaf/42076980
Preferred Forms
- 100 0 _ ‡a Gérard Tachdjian ‡c médecin français
- 200 _ | ‡a Tachdjian ‡b Gérard
- 100 1 _ ‡a Tachdjian, Gérard
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- 100 1 _ ‡a Tachdjian, Gérard
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4xx's: Alternate Name Forms (2)
Works
Title | Sources |
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AMH signaling pathway and its target genes in female reproductive tract. | |
Analyse des variations du nombre de copies d'ADN dans une cohorte d'hommes infertiles et génération de modèles génétiques d'étude de la méiose à partir de cellules iPS de patients infertiles | |
Analyse moléculaire du syndrome de persistance des canaux de Müller | |
Anophthalmia, hearing loss, abnormal pituitary development and response to growth hormone therapy in three children with microdeletions of 14q22q23 | |
Apport de l'hybridation génomique comparative sur puce à ADN pour l'étude cytogénétique des anomalies du développement humain | |
Array comparative genomic hybridization analysis of small supernumerary marker chromosomes in human infertility. | |
An atypical human induced pluripotent stem cell line with a complex, stable, and balanced genomic rearrangement including a large de novo 1q uniparental disomy. | |
The cAMP pathway in Schwann cell behavior and peripheral myelination. | |
La cellule et les tissus : UE 2 | |
Les cellules souches embryonnaires humaines, un modèle d'étude des étapes précoces de la lymphopoïèse | |
Complex translocation t(1;12;14)(q42;q14;q32) and HMGA2 deletion in a fetus presenting growth delay and bilateral cataracts. | |
Confined blood chimerism in a monochorionic dizygotic sex discordant twin pregnancy conceived after induced ovulation | |
Contribution of comparative genomic hybridization on DNA microarrays for the cytogenetic study of the human development anomalies. | |
Détermination du taux d'aneuploi͏̈die pour les chromosomes 8, 9, 13, 18, 21, X et Y dans les spermatozoi͏̈des de patients présentant des echecs répétés d'implantation aprés ICSI | |
Disrupted filamin A/αβ interaction induces macrothrombocytopenia by increasing RhoA activity | |
DNA copy number variations study in a cohort of infertile men and generation of an in vitro model for the study of meiosis from infertile patient's iPS cells. | |
Du chromosome au gène par un criblage global des altérations génomiques dans la malignité pour isoler de nouvelles cibles thérapeutiques | |
Embryologie et histologie humaines | |
Embryonic and somatic reprogramming at the time of embryonic genome activation in the bovine embryo. | |
Etude de la corrélation entre la morphologie ovocytaire, le développement embryonnaire et les taux de grossesse après ICSI | |
Facteurs morphologiques et génétiques impliqués dans le développement de l'embryon humain et la dérivation de cellules souches embryonnaires | |
LES FRAGMENTS CHROMOSOMIQUES SURNUMERAIRES : A PROPOS D'UNE OBSERVATION FAMILIALE | |
From Chromosome to Gene by Mapping Chromosomal Abnormalities in Cancer in Order to Find Targeted Pharmaceutical Agents. | |
Genomic instability of human embryonic stem cell lines using different passaging culture methods. | |
Human embryonic stem cells, a model to study the early steps of lymphopoiesis. | |
Implication of the IRXB cluster genes in the anterior segment ocular dysgenesis. | |
Induced pluripotent stem cell generation from a man carrying a complex chromosomal rearrangement as a genetic model for infertility studies | |
Inherited 1q21.1q21.2 duplication and 16p11.2 deletion: a two-hit case with more severe clinical manifestations | |
L'assistance médicale à la procréation | |
Level of RUNX1 activity is critical for leukemic predisposition but not for thrombocytopenia. | |
Messenger RNA- versus retrovirus-based induced pluripotent stem cell reprogramming strategies: analysis of genomic integrity. | |
Modeling the influence of stromal microenvironment in the selection of ENU-induced BCR-ABL1 mutants by tyrosine kinase inhibitors. | |
Molecular cytogenetics applications to human diseases. | |
Prenatal Diagnosis of a 2.5 Mb De Novo 17q24.1q24.2 Deletion Encompassing KPNA2 and PSMD12 Genes in a Fetus with Craniofacial Dysmorphism, Equinovarus Feet, and Syndactyly | |
Reprogrammation embryonnaire et somatique au moment de la mise en route du génome dans l'embryon bovin | |
Risk of tumorigenicity in mesenchymal stromal cell-based therapies--bridging scientific observations and regulatory viewpoints | |
Rôles des androgènes et de leur récepteur AR dans le dimorphisme et la réparation de la myéline | |
SALL4 and NFATC2: two major actors of interstitial 20q13.2 duplication. | |
SEMA3A deletion in a family with Kallmann syndrome validates the role of semaphorin 3A in human puberty and olfactory system development | |
Shortening gametes co-incubation time improves live birth rate for couples with a history of fragmented embryos. | |
Small supernumerary marker chromosomes derived from chromosomes 6 and 20 in a woman with recurrent spontaneous abortions. | |
Study of the correlation between the oocyte morphology, the embryonic development and the pregnancy rates after ICSI. | |
Tetrasomy 13q31.1qter due to an inverted duplicated neocentric marker chromosome in a fetus with multiple malformations | |
Towards a clinical use of human embryonic stem cell-derived cardiac progenitors: a translational experience | |
Transplantation of Macaca cynomolgus iPS-derived hematopoietic cells in NSG immunodeficient mice | |
La voie de l'AMPc dans le comportement des cellules de Schwann et la myélinisation périphérique | |
Voie de signalisation et gènes cibles de l'AMH dans le tractus génital femelle | |
WAGR syndrome and congenital hypothyroidism in a child with a Mosaic 11p13 deletion. |