Qinjie Tian

Summary

Publications

  1. ncbi request reprint Development of low-dose reproductive hormone therapies in China
    Qinsheng Ge
    Division of Reproductive Endocrinology, Department of Obstetrics and Gynecology, Peking Union Medical College Hospital, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing, China
    Gynecol Endocrinol 22:636-45. 2006
  2. doi request reprint Partial 17alpha-hydroxylase/17,20-lyase deficiency-clinical report of five Chinese 46,XX cases
    Qinjie Tian
    Department of Obstetrics and Gynecology, Peking Union Medical College Hospital, Chinese Academy of Medical Science, Beijing, People s Republic of China
    Gynecol Endocrinol 24:362-7. 2008
  3. doi request reprint Gender verification in athletes with disorders of sex development
    Qinjie Tian
    Division of Reproductive Endocrinology, Department of Obstetrics and Gynecology, Peking Union Medical College Hospital, Peking Union Medical College, Chinese Academy of Medical Science, Beijing, China
    Gynecol Endocrinol 25:117-21. 2009
  4. doi request reprint Genotyping of a Chinese family with 46,XX and 46,XY 17-hydroxylase deficiency
    Qinjie Tian
    Department of Obstetrics and Gynecology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China
    Gynecol Endocrinol 25:485-90. 2009
  5. doi request reprint CYP17A1 mutations identified in 17 Chinese patients with 17α-hydroxylase/17,20-lyase deficiency
    Fengxia Yao
    Clinical Research Lab, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, People s Republic of China
    Gynecol Endocrinol 29:10-5. 2013
  6. doi request reprint Molecular study of five Chinese patients with 46XX partial 17a-hydroxylase/17,20-lyase deficiency
    Qinjie Tian
    Peking Union Medical College Hospital, Department of Obstetrics and Gynecology, Beijing, China
    Gynecol Endocrinol 28:234-8. 2012

Collaborators

Detail Information

Publications6

  1. ncbi request reprint Development of low-dose reproductive hormone therapies in China
    Qinsheng Ge
    Division of Reproductive Endocrinology, Department of Obstetrics and Gynecology, Peking Union Medical College Hospital, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing, China
    Gynecol Endocrinol 22:636-45. 2006
    ..These results highlight the urgent need for larger, prospective trials of long-term low-dose HRT started during the perimenopausal period...
  2. doi request reprint Partial 17alpha-hydroxylase/17,20-lyase deficiency-clinical report of five Chinese 46,XX cases
    Qinjie Tian
    Department of Obstetrics and Gynecology, Peking Union Medical College Hospital, Chinese Academy of Medical Science, Beijing, People s Republic of China
    Gynecol Endocrinol 24:362-7. 2008
    ..To summarize the clinical characteristics of partial 17alpha-hydroxylase/17,20-lyase deficiency (17OHD) in 46,XX Chinese patients...
  3. doi request reprint Gender verification in athletes with disorders of sex development
    Qinjie Tian
    Division of Reproductive Endocrinology, Department of Obstetrics and Gynecology, Peking Union Medical College Hospital, Peking Union Medical College, Chinese Academy of Medical Science, Beijing, China
    Gynecol Endocrinol 25:117-21. 2009
    ....
  4. doi request reprint Genotyping of a Chinese family with 46,XX and 46,XY 17-hydroxylase deficiency
    Qinjie Tian
    Department of Obstetrics and Gynecology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China
    Gynecol Endocrinol 25:485-90. 2009
    ..17-Hydroxylase deficiency is a rare form of congenital adrenal hyperplasia caused by CYP17A1 gene mutations...
  5. doi request reprint CYP17A1 mutations identified in 17 Chinese patients with 17α-hydroxylase/17,20-lyase deficiency
    Fengxia Yao
    Clinical Research Lab, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, People s Republic of China
    Gynecol Endocrinol 29:10-5. 2013
    ..Human CYP17A1 gene is located on chromosome 10q24.3. It consists of eight exons encoding 508 amino acids. To date, more than 50 mutations in exons and introns of the CYP17A1 gene have been reported to cause complete or partial 17OHD...
  6. doi request reprint Molecular study of five Chinese patients with 46XX partial 17a-hydroxylase/17,20-lyase deficiency
    Qinjie Tian
    Peking Union Medical College Hospital, Department of Obstetrics and Gynecology, Beijing, China
    Gynecol Endocrinol 28:234-8. 2012
    ..Partial 17a-hydroxylase/17,20 lyase deficiency (17OHD) is a rare subtype of 17OHD caused by CYP17 gene mutations...