19 results on '"Zhang, Xianqin"'
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2. Novel splicing mutations in PATL2 and WEE2 cause oocyte degradation and fertilization failure
3. A Mettl16/m6A/mybl2b/Igf2bp1 axis ensures cell cycle progression of embryonic hematopoietic stem and progenitor cells
4. A novel mutation in the GALC gene causes Krabbe disease accompanied with extensive Mongolian spots in a consanguineous family
5. A novel homozygous mutation in ACTL7A leads to male infertility
6. Coexistence of tet(A) and blaKPC-2 in the ST11 hypervirulent tigecycline- and carbapenem-resistant Klebsiella pneumoniae isolated from a blood sample
7. A Novel Homozygous Nonsense Mutation in ZP1 Causes Female Infertility due to Empty Follicle Syndrome
8. Novel Heterozygous Mutations in ZP2 Cause Abnormal Zona Pellucida and Female Infertility
9. Novel Compound Heterozygous Mutation in FSIP2 Causes Multiple Morphological Abnormalities of the Sperm Flagella (MMAF) and Male Infertility
10. Novel mutations in ZP2 and ZP3 cause female infertility in three patients
11. TUBB8 Mutations Cause Female Infertility with Large Polar Body Oocyte and Fertilization Failure
12. A novel mutation in ZP3 causes empty follicle syndrome and abnormal zona pellucida formation
13. Novel mutations in ZP1 and ZP2 cause primary infertility due to empty follicle syndrome and abnormal zona pellucida
14. Deficiency of SCAMP5 leads to pediatric epilepsy and dysregulation of neurotransmitter release in the brain
15. Novel compound heterozygous mutations in WEE2 causes female infertility and fertilization failure
16. SLCO4C1 promoter methylation is a potential biomarker for prognosis associated with biochemical recurrence-free survival after radical prostatectomy
17. FOXS1 is regulated by GLI1 and miR-125a-5p and promotes cell proliferation and EMT in gastric cancer
18. Identification of a new lamin A/C mutation in a chinese family affected with atrioventricular block as the prominent phenotype
19. Novel CACNA1S mutation causes autosomal dominant hypokalemic periodic paralysis in a Chinese family
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