23 results on '"Zhang, Xianqin"'
Search Results
2. A novel mutation in the GALC gene causes Krabbe disease accompanied with extensive Mongolian spots in a consanguineous family
3. A novel homozygous mutation in ACTL7A leads to male infertility
4. Coexistence of tet(A) and blaKPC-2 in the ST11 hypervirulent tigecycline- and carbapenem-resistant Klebsiella pneumoniae isolated from a blood sample
5. A Novel Homozygous Nonsense Mutation in ZP1 Causes Female Infertility due to Empty Follicle Syndrome
6. Novel Compound Heterozygous Mutation in FSIP2 Causes Multiple Morphological Abnormalities of the Sperm Flagella (MMAF) and Male Infertility
7. Novel Heterozygous Mutations in ZP2 Cause Abnormal Zona Pellucida and Female Infertility
8. Novel mutations in ZP2 and ZP3 cause female infertility in three patients
9. TUBB8 Mutations Cause Female Infertility with Large Polar Body Oocyte and Fertilization Failure
10. A novel mutation in ZP3 causes empty follicle syndrome and abnormal zona pellucida formation
11. Novel mutations in ZP1 and ZP2 cause primary infertility due to empty follicle syndrome and abnormal zona pellucida
12. Novel homozygous mutations in PATL2 lead to female infertility with oocyte maturation arrest
13. Deficiency of SCAMP5 leads to pediatric epilepsy and dysregulation of neurotransmitter release in the brain
14. Novel compound heterozygous mutations in WEE2 causes female infertility and fertilization failure
15. SLCO4C1 promoter methylation is a potential biomarker for prognosis associated with biochemical recurrence-free survival after radical prostatectomy
16. FOXS1 is regulated by GLI1 and miR-125a-5p and promotes cell proliferation and EMT in gastric cancer
17. Bacterial metabolites directly modulate farnesoid X receptor activity
18. Erratum: Human intracellular ISG15 prevents interferon-α/β over-amplification and auto-inflammation
19. Human intracellular ISG15 prevents interferon-α/β over-amplification and auto-inflammation
20. Identification of a new lamin A/C mutation in a chinese family affected with atrioventricular block as the prominent phenotype
21. Protective effect of KCNH2 single nucleotide polymorphism K897T in LQTS families and identification of novel KCNQ1 and KCNH2mutations
22. A novel DSPPmutation is associated with type II dentinogenesis Imperfecta in a chinese family
23. Novel CACNA1S mutation causes autosomal dominant hypokalemic periodic paralysis in a Chinese family
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