1996
DOI: 10.1093/humrep/11.suppl_5.95
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Clinical assessment of human gonadotrophins produced by recombinant DNA technology

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Cited by 44 publications
(32 citation statements)
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“…More recently recombinant hormones have also been developed with a similar activity profile. 105 Deglycosylated hCG has been described as an antagonist of the LH receptor. 106 Recently, another hormonal antagonist was identified, which was generated by fusing two hCG b-subunits.…”
Section: L H R E C E P T O R a G O N I S T Smentioning
confidence: 99%
See 1 more Smart Citation
“…More recently recombinant hormones have also been developed with a similar activity profile. 105 Deglycosylated hCG has been described as an antagonist of the LH receptor. 106 Recently, another hormonal antagonist was identified, which was generated by fusing two hCG b-subunits.…”
Section: L H R E C E P T O R a G O N I S T Smentioning
confidence: 99%
“…Urinary and recombinant FSH is also used in the treatment of infertility. 105 Recombinant gonadotropins need to be administered daily and therefore effort was made to develop gonadotropins with a longer half-life. Long-acting FSH may be produced by fusing the carboxyl terminal extension of the b-subunit of hCG to the b-subunit of FSH or by additional glycosylation of FSH.…”
Section: F S H R E C E P T O R L I G a N D Smentioning
confidence: 99%
“…Subcutaneous rhCG has been recently introduced for final follicular maturation and ovulation induction in infertile women undergoing ART. rhCG preparations are derived from genetically engineered Chinese hamster ovary cells through recombinant DNA technology [5]. This product is purified by repeated chromatographic steps to produce a high specific activity outcome which makes the drug free from urinary contaminations and suitable for subcutaneous injection and self administration with lower local reactions and higher tolerability [6][7][8].…”
Section: Introductionmentioning
confidence: 99%
“…The consulting physician was blinded as to the randomization arm of the patient, and all the patients gave their signed informed consent. Inclusion criteria were: [1] female age <36 years, [2] rank trial %2, [3] FSH on day 3 of the cycle %12 IU/mL, [4] male or tubal infertility, and [5] one embryo (n ¼ 1) at the blastocyst stage to be transferred in each group. The primary outcome was the blastulation rate.…”
mentioning
confidence: 99%