Hasil Pencarian - Shanling Liu

Perbaiki Hasil
  1. 1
    Factors Affecting the Fetal Fraction in Noninvasive Prenatal Screening: A Review

    Factors Affecting the Fetal Fraction in Noninvasive Prenatal Screening: A Review oleh Cechuan Deng, Cechuan Deng, Shanling Liu, Shanling Liu

    Diterbitkan 2022-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  2. 2
    Potentials and challenges of chromosomal microarray analysis in prenatal diagnosis

    Potentials and challenges of chromosomal microarray analysis in prenatal diagnosis oleh Xijing Liu, Xijing Liu, Xijing Liu, Shanling Liu, Shanling Liu, Shanling Liu, He Wang, He Wang, He Wang, Ting Hu, Ting Hu, Ting Hu

    Diterbitkan 2022-07-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  3. 3
    Case Report: Novel Compound Heterozygous Variants in TRIOBP Associated With Congenital Deafness in a Chinese Family

    Case Report: Novel Compound Heterozygous Variants in TRIOBP Associated With Congenital Deafness in a Chinese Family oleh Cong Zhou, Cong Zhou, Yuanyuan Xiao, Yuanyuan Xiao, Hanbing Xie, Hanbing Xie, Jing Wang, Jing Wang, Shanling Liu, Shanling Liu

    Diterbitkan 2021-11-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  4. 4
    A novel USH2A variant in a patient with hearing loss and prenatal diagnosis of a familial fetus: a case report

    A novel USH2A variant in a patient with hearing loss and prenatal diagnosis of a familial fetus: a case report oleh Cong Zhou, Yuanyuan Xiao, Hanbing Xie, Shanling Liu, Jing Wang

    Diterbitkan 2021-08-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  5. 5
    Expression of ITPR2 regulated by lncRNA-NONMMUT020270.2 in LPS-stimulated HT22 cells

    Expression of ITPR2 regulated by lncRNA-NONMMUT020270.2 in LPS-stimulated HT22 cells oleh Lan Liu, Liang Tang, Yan Wang, Shanling Liu, Yongcang Zhang

    Diterbitkan 2024-07-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  6. 6
    Enhanced antifungal activity of bovine lactoferrin-producing probiotic Lactobacillus casei in the murine model of vulvovaginal candidiasis

    Enhanced antifungal activity of bovine lactoferrin-producing probiotic Lactobacillus casei in the murine model of vulvovaginal candidiasis oleh Hong Liao, Shanling Liu, He Wang, Hang Su, Zhenjun Liu

    Diterbitkan 2019-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  7. 7
    Case Report: Whole exome sequencing identifies compound heterozygous variants in the TRAPPC9 gene in a child with developmental delay

    Case Report: Whole exome sequencing identifies compound heterozygous variants in the TRAPPC9 gene in a child with developmental delay oleh Bingxuan Yu, Bingxuan Yu, Jing Chen, Jing Chen, Shuo Yang, Shuo Yang, He Wang, He Wang, Yuanyuan Xiao, Yuanyuan Xiao, Shanling Liu, Shanling Liu

    Diterbitkan 2024-08-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  8. 8
    Case report: Whole exome sequencing reveals a novel splicing variant of ANKRD17 gene in a Chinese male juvenile with developmental delay and transient tic disorder

    Case report: Whole exome sequencing reveals a novel splicing variant of ANKRD17 gene in a Chinese male juvenile with developmental delay and transient tic disorder oleh Jing Chen, Jing Chen, Shuo Yang, Shuo Yang, He Wang, He Wang, Hongjing Wang, Hongjing Wang, Yuanyuan Xiao, Yuanyuan Xiao, Shanling Liu, Shanling Liu

    Diterbitkan 2024-09-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  9. 9
    Case report: Genetic diagnoses in a pediatric patient with retinoblastoma and comorbid global developmental delay: three distinct entities diagnosed by whole exome sequencing in a single patient

    Case report: Genetic diagnoses in a pediatric patient with retinoblastoma and comorbid global developmental delay: three distinct entities diagnosed by whole exome sequencing in a... oleh Jing Chen, Jing Chen, Shuo Yang, Shuo Yang, He Wang, He Wang, Hongjing Wang, Hongjing Wang, Yuanyuan Xiao, Yuanyuan Xiao, Shanling Liu, Shanling Liu

    Diterbitkan 2024-07-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  10. 10
    Natural phytochemicals prevent side effects in BRCA-mutated ovarian cancer and PARP inhibitor treatment

    Natural phytochemicals prevent side effects in BRCA-mutated ovarian cancer and PARP inhibitor treatment oleh Chuanlin Wang, Chuanlin Wang, Pengning Gao, Pengning Gao, Jiali Xu, Jiali Xu, Shanling Liu, Shanling Liu, Wenda Tian, Wenda Tian, Jiayu Liu, Lan Zhou, Lan Zhou

    Diterbitkan 2022-12-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  11. 11
    Novel compound heterozygous variants in lectin mannose-binding 2-like gene identified in a Chinese autosomal recessive mental retardation-52 (MRT52) patient with phenotype expansion

    Novel compound heterozygous variants in lectin mannose-binding 2-like gene identified in a Chinese autosomal recessive mental retardation-52 (MRT52) patient with phenotype expansio... oleh Cong Zhou, Xing Wei, Yuanyuan Xiao, Shanling Liu, Jing Wang, Jing Ni

    Diterbitkan 2023-09-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  12. 12
    HIV-1-related factors interact with p53 to influence cellular processes

    HIV-1-related factors interact with p53 to influence cellular processes oleh Shanling Liu, Ting Guo, Jinwei Hu, Weiliang Huang, Pengfei She, Yong Wu

    Diterbitkan 2023-09-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  13. 13
    NGS-based targeted sequencing identified two novel variants in Southwestern Chinese families with oculocutaneous albinism

    NGS-based targeted sequencing identified two novel variants in Southwestern Chinese families with oculocutaneous albinism oleh Yuanyuan Xiao, Cong Zhou, Hanbing Xie, Shuang Huang, Jing Wang, Shanling Liu

    Diterbitkan 2022-04-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  14. 14
    A novel deletion mutation in the BCOR gene is associated with oculo-facio-cardio-dental syndrome: a case report

    A novel deletion mutation in the BCOR gene is associated with oculo-facio-cardio-dental syndrome: a case report oleh Qian Hu, Jingqun Mai, Qinqin Xiang, Bin Zhou, Shanling Liu, Jing Wang

    Diterbitkan 2022-02-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  15. 15
    Case report: A novel de novo deletion mutation of DYRK1A is associated with intellectual developmental disorder, autosomal dominant 7

    Case report: A novel de novo deletion mutation of DYRK1A is associated with intellectual developmental disorder, autosomal dominant 7 oleh Cong Zhou, Cong Zhou, Hongmei Zhu, Hongmei Zhu, Qinqin Xiang, Qinqin Xiang, Jingqun Mai, Jingqun Mai, Xihan Wang, Xihan Wang, Jing Wang, Jing Wang, Shanling Liu, Shanling Liu

    Diterbitkan 2023-05-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  16. 16
    Case Report: The compound heterozygotes variants in FLT4 causes autosomal recessive hereditary lymphedema in a Chinese family

    Case Report: The compound heterozygotes variants in FLT4 causes autosomal recessive hereditary lymphedema in a Chinese family oleh Qinqin Xiang, Qinqin Xiang, Qinqin Xiang, Jing Chen, Jing Chen, Jing Chen, Xiao Xiao, Xiao Xiao, Xiao Xiao, Bocheng Xu, Bocheng Xu, Bocheng Xu, Hanbing Xie, Hanbing Xie, Hanbing Xie, He Wang, He Wang, He Wang, Mei Yang, Mei Yang, Mei Yang, Shanling Liu, Shanling Liu, Shanling Liu

    Diterbitkan 2023-03-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  17. 17
    A novel heterozygous PKD1 variant causing alternative splicing in a Chinese family with autosomal dominant polycystic kidney disease

    A novel heterozygous PKD1 variant causing alternative splicing in a Chinese family with autosomal dominant polycystic kidney disease oleh Qianying Zhao, Yu Tan, Xiao Xiao, Qinqin Xiang, Mei Yang, He Wang, Shanling Liu

    Diterbitkan 2023-08-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  18. 18
    Case report: Prenatal diagnosis of rare chromosome mosaicism: discordant results between chorionic villi and amniotic fluid samples

    Case report: Prenatal diagnosis of rare chromosome mosaicism: discordant results between chorionic villi and amniotic fluid samples oleh Lingping Li, Lingping Li, Lingping Li, Xijing Liu, Xijing Liu, Xijing Liu, Qinqin Li, Qinqin Li, Qinqin Li, Lili Zhang, Lili Zhang, Lili Zhang, Yueyue Xiong, Yueyue Xiong, Yueyue Xiong, Shanling Liu, Shanling Liu, Shanling Liu, He Wang, He Wang, He Wang, Hongmei Zhu, Hongmei Zhu, Hongmei Zhu, Xuemei Zhang, Xuemei Zhang, Xuemei Zhang

    Diterbitkan 2023-06-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  19. 19
    Case Report: Preimplantation Genetic Testing for X-Linked Severe Combined Immune Deficiency Caused by IL2RG Gene Variant

    Case Report: Preimplantation Genetic Testing for X-Linked Severe Combined Immune Deficiency Caused by IL2RG Gene Variant oleh Jun Ren, Jun Ren, Jun Ren, Cuiting Peng, Cuiting Peng, Cuiting Peng, Fan Zhou, Fan Zhou, Fan Zhou, Yutong Li, Yutong Li, Yutong Li, Yuezhi Keqie, Yuezhi Keqie, Yuezhi Keqie, Han Chen, Han Chen, Han Chen, Hongmei Zhu, Hongmei Zhu, Hongmei Zhu, Xinlian Chen, Xinlian Chen, Xinlian Chen, Shanling Liu, Shanling Liu, Shanling Liu

    Diterbitkan 2022-06-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  20. 20
    Carrying both COL1A2 and FBN2 gene heterozygous mutations results in a severe skeletal clinical phenotype: an affected family

    Carrying both COL1A2 and FBN2 gene heterozygous mutations results in a severe skeletal clinical phenotype: an affected family oleh Jing Chen, Qinqin Xiang, Xiao Xiao, Bocheng Xu, Hanbing Xie, He Wang, Mei Yang, Shanling Liu

    Diterbitkan 2022-07-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:

Alat Pencarian: