712 results on '"Fellous, M."'
Search Results
2. Loss of Sequences 3′ to the Testis-Determining Gene, SRY, Including the Y Pseudoautosomal Boundary Associated with Partial Testicular Determination
3. EP08.02-148 Extended Follow-up of Efficacy and Safety of Larotrectinib in Patients With TRK Fusion Lung Cancer
4. SO-31 Long-term efficacy and safety of larotrectinib in patients with tropomyosin receptor kinase (TRK) fusion gastrointestinal (GI) cancer: An expanded dataset
5. 61P Updated efficacy and ctDNA analysis of patients with TRK fusion lung cancer treated with larotrectinib
6. A non-sense MCM9 mutation in a familial case of primary ovarian insufficiency
7. 536P Incidence of fractures in TRK fusion cancer patients treated with larotrectinib
8. 104P Matching-adjusted indirect comparison for treatment of NTRK fusion cancer with larotrectinib versus entrectinib
9. 534P Larotrectinib in non-CNS TRK fusion cancer patients: Outcomes by prior therapy and performance status
10. Tumeurs juvéniles de la granulosa : expression clinique et moléculaire
11. Human Chromosome 16 Encodes a Factor Involved in Induction of Class II Major Histocompatibility Antigens by Interferon γ
12. Genetic Counseling for the Orthodox Jewish Couple Undergoing Preimplantation Genetic Diagnosis
13. Analyse génétique des insuffisances ovariennes prématurées : implication des gènes forkhead et TGF-β
14. Deletions involving long-range conserved nongenic sequences upstream and downstream of FOXL2 as a novel disease-causing mechanism in blepharophimosis syndrome
15. PCN178 Challenges of Descriptive Epidemiology in RARE Diseases: A Systematic Literature Review (SLR) and Meta-Analysis (MA) of SOLID Tumors with Neurotrophic Tyrosine Receptor Kinase (NTRK) GENE Fusions
16. Linkage and association of the glutamate receptor 6 gene with autism
17. 604TiP ON-TRK: A non-interventional study of larotrectinib in patients with TRK fusion cancer
18. 542P Growth modulation index (GMI) of larotrectinib versus prior systemic treatments for TRK fusion cancer patients
19. Co-occurrence of NTRK fusions with other genomic biomarkers in cancer patients
20. Growth modulation index (GMI) as a comparative measure of clinical activity of larotrectinib versus prior systemic treatments in adult and pediatric TRK fusion cancer patients
21. Functional evidence implicating FOXL2 in non-syndromic premature ovarian failure and in the regulation of the transcription factor OSR2
22. Mutations and sequence variants in the testis-determining region of the Y chromosome in individuals with a 46,XY female phenotype
23. Interferon alpha inhibits a Src-mediated pathway necessary for Shigella-induced cytoskeletal rearrangements in epithelial cells
24. FOXL2 and SOX9 as parameters of female and male gonadal differentiation in patients with various forms of disorders of sex development (DSD)#
25. Genetic mapping of the autosomal region involved in XX sex-reversal and horn development in goats
26. Swyer syndrome and 46,XY partial gonadal dysgenesis associated with 9p deletions in the absence of monosomy-9p syndrome
27. Population Structure in the Mediterranean Basin: A Y Chromosome Perspective
28. Hormonal and molecular genetic findings in 46,XX subjects with sexual ambiguity and testicular differentiation
29. Genetics analysis of human infertility
30. Y chromosome haplogroups in autistic subjects
31. A Glycolipid Antigen Associated with Burkitt Lymphoma Defined by a Monoclonal Antibody
32. A recurrent polyalanine expansion in the transcription factor FOXL2 induces extensive nuclear and cytoplasmic protein aggregation
33. GermOnline, a cross-species community knowledgebase on germ cell differentiation
34. Evolution and expression of FOXL2
35. Transmission of an unbalanced (Y;1) translocation in Brittany, France
36. FOXL2 mutation screening in a large panel of POF patients and XX males
37. Deletion of 9p associated with gonadal dysfunction in 46,XY but not in 46,XX human fetuses
38. A High Frequency of Y Chromosome Deletions in Males with Nonidiopathic Infertility*
39. Infertilité masculine et les microdélétions du chromosome Y
40. SRY-negative XX fetus with complete male phenotype
41. Association of FOXD1 variants with adverse pregnancy outcomes in mice and humans
42. Relationship Between Y-Chromosome and H-Y Antigen Expression in Human Spermatozoa
43. Expression and Characterization of Leucocyte Antigens
44. 485P - Growth modulation index (GMI) as a comparative measure of clinical activity of larotrectinib versus prior systemic treatments in adult and pediatric TRK fusion cancer patients
45. 102P - Co-occurrence of NTRK fusions with other genomic biomarkers in cancer patients
46. P-015: Association of FOXD1 variants with pregnancy failures in mice and humans
47. Identification of human SRY-interacting factors
48. Cloacal extrophy in an infant with 9q34-qter deletion resulting from a de novo unbalanced tranlocation between chromosome 9q and Yq
49. Spectrum and distribution of FOXL2 gene mutations and variants in BPES, POF and XX male patients: tentative genotype-phenotype correlation
50. Linkage and association of the glutamate receptor 6 gene with autism
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