562 results on '"Fellous, Marc"'
Search Results
102. Timing of multikinase inhibitor initiation in differentiated thyroid cancer
103. Association of FOXD1 variants with adverse pregnancy outcomes in mice and humans
104. Association of FOXD1 variants with adverse pregnancy outcomes in mice and humans
105. Genome Editing and Dialogic Responsibility: “What's in a Name?”
106. Further cytologic evidence for Xp-Yp translocation in XX males using in situ hybridization with Y-derived probe
107. Phenotype and surface antigens of mouse teratocarcinoma × fibroblast cell hybrids
108. Monoclonal antibodies as a tool for phylogenetic studies of major histocompatibility antigens and β 2-microglobulin
109. Distinctive properties of fucosyl glycopeptides on human teratoma cells
110. Induction of HLA expression in Daudi cells after cell fusion
111. Presence of an abnormal β 2-microglobulin mRNA in Daudi cells: Induction by interferon
112. Abnormal ovarian morphogenesis in Drosophila melanogaster after injection of embryos with conditioned media from the Daudi cell line
113. HLA-DR-specific monoclonal antibodies cross-react with several self and nonself non-MHC molecules
114. Prendre la mesure d’une culture ouverte et responsable
115. INTERFERON-INDUCED PROTEINS: BIOLOGICAL FUNCTIONS AND CLINICAL APPLICATIONS11This work was supported in part by NCRD (Israel) and GSF (Germany), and in part by InterYeda (Israel).
116. Human genetic of premature ovarian failure: a mendelian and candidate genes approach
117. Human interferon gamma receptor 1 (IFNGR1) gene maps to chromosome region 6q23–6q24
118. Molecular aspects of female and male gonodal development in mammals
119. Final analysis of European patients from the Global Investigation of Therapeutic Decisions in Hepatocellular Carcinoma and of its Treatment with Sorafenib (GIDEON) study: Baseline characteristics and staging systems.
120. Emmanuel Adrien Nunez (1934–2013) vient de nous quitter
121. Molecular genetics of sex determination
122. Linkage and association of the glutamate receptor 6 gene with autism
123. Génétique et infertilité humaine : 'une approche gènes candidats'
124. Le déterminisme du sexe : son contrôle génetique
125. The Human Y Chromosome: The Biological Role of a 'Functional Wasteland'
126. Contribution of domestic animals to the identification of new genes involved in sex determination
127. A 11.7-kb delection triggers intersexuality and polledness in goats
128. sY116, a human Y-linked polymorphic STS
129. Identification of 34 novel and 56 known FOXL2 mutations in patients with Blepharophimosis syndrome.
130. Sex reversal in man and domestic animal. Contribution to the understanding of mammalian sex differentiation
131. Disruption of the principal, progesterone-activated sperm Ca 2+ channel in a CatSper2-deficient infertile patient
132. Genetic mapping of the polled/intersex locus (PIS) in goats
133. Genome-Wide Linkage in a Highly Consanguineous Pedigree Reveals Two Novel Loci on Chromosome 7 for Non-Syndromic Familial Premature Ovarian Failure
134. Physiological and genetical study of polled/intersex goats. Genetic mapping of the chromosomal region involved
135. Distinct domains of the protein tyrosine kinase tyk2 required for binding of interferon-a/b and for signal transduction
136. Analyse moléculaire de chèvres 60, XX pseudohermaphrodite sans corne pour la présence de gènes SRY et ZFY
137. Genetic male infertility and mutation of CATSPER ion channels
138. Functional Exploration of the Adult Ovarian Granulosa Cell Tumor-Associated Somatic FOXL2 Mutation p.Cys134Trp (c.402C>G)
139. The transcription factor FOXL2 in ovarian function and dysfunction.
140. Sex determination : genetic control
141. Antagonism of the testis- and ovary-determining pathways during ovotestis development in mice
142. Identification of Quantitative Trait Loci responsible for embryonic lethality in mice assessed by ultrasonography
143. GMO risk assessment around the world: Some examples
144. Identification of 34 novel and 56 knownFOXL2mutations in patients with blepharophimosis syndrome
145. Genetic investigation of four meiotic genes in women with premature ovarian failure
146. Recent advances in the study of genes involved in non-syndromic premature ovarian failure
147. La determination du sexe dans l'espece humaine
148. FOXO3a variants in patients with premature ovarian failure
149. Recovery of Female Fertility After Chemotherapy, Irradiation, and Bone Marrow Allograft: Further Evidence Against Massive Oocyte Regeneration by Bone Marrow-Derived Germline Stem Cells
150. Mutations and sequence variants in GDF9 and BMP15 in patients with premature ovarian failure
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