S. Samuel Kim
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Research Interests
S. Samuel Kim has a total of 13 co-authors. Here are the top co-authors by number of shared publications:
Hoi Chang Lee
2 shared publicationsDavid E Battaglia
1 shared publicationDuck Sung Ko
1 shared publicationHang Heun Lee
1 shared publicationHee Gyoo Kang
1 shared publicationHee Gyu Kang
1 shared publication
Latest Publications
- 1 January 2006
- Published by Elsevier in Fertility and Sterility
- Vol. 85 (1) , 1-11
Fertility preservation in female cancer patients: current developments and future directions
- 1 January 2006
- Published by Elsevier in Fertility and Sterility
- Vol. 85 (1) , 1-11
Fertility preservation in female cancer patients: current developments and future directions
- Open Access
- 9 June 2005
- Published by Oxford University Press (OUP) in Human Reproduction
- Vol. 20 (9) , 2502-2508
Assessment of the integrity of human oocytes retrieved from cryopreserved ovarian tissue after xenotransplantation
BACKGROUND: Previous studies showed that immature oocytes stored in ovarian tissue could develop to the mature stage after transplantation. However, the quality and competency of the oocytes developed in xenografted ovarian tissue have never been investigated. As a pilot study to investigate this uncharted issue, we evaluated microtubule organization and chromatin configuration of human oocytes harvested from xenografted frozen–thawed ovarian tissue. METHODS: Frozen–thawed human ovarian tissue was transplanted into severe combined immunodeficient mice. All animals were stimulated with gonadotrophin from 20 weeks after transplantation. Grafts were recovered 36 h after hCG administration. The oocytes were retrieved from the antral follicles (>2 mm diameter), cultured in vitro, stained for microtubule and chromatin localization. RESULTS: Five oocytes from 21 female mice and seven oocytes from nine male mice were retrieved. Immunocytochemical examinations of these oocytes after in vitro maturation revealed only two developed to the metaphase II stage. Most oocytes were between prophase and metaphase with abnormal microtubule organization and chromatin configuration. CONCLUSIONS: Immature oocytes in stored human ovarian tissue can grow to maturity in host animals after xenotransplantation. Retrieval of oocytes from the xenograft can be carried out and is reproducible. However, many oocytes, grown in host animals and further matured in vitro, showed aberrant microtubule organization and chromatin patterns.
- 9 June 2005
- Published by Oxford University Press (OUP) in Human Reproduction
- Vol. 20 (9) , 2502-2508
Open AccessAssessment of the integrity of human oocytes retrieved from cryopreserved ovarian tissue after xenotransplantation
BACKGROUND: Previous studies showed that immature oocytes stored in ovarian tissue could develop to the mature stage after transplantation. However, the quality and competency of the oocytes developed in xenografted ovarian tissue have never been investigated. As a pilot study to investigate this uncharted issue, we evaluated microtubule organization and chromatin configuration of human oocytes harvested from xenografted frozen–thawed ovarian tissue. METHODS: Frozen–thawed human ovarian tissue was transplanted into severe combined immunodeficient mice. All animals were stimulated with gonadotrophin from 20 weeks after transplantation. Grafts were recovered 36 h after hCG administration. The oocytes were retrieved from the antral follicles (>2 mm diameter), cultured in vitro, stained for microtubule and chromatin localization. RESULTS: Five oocytes from 21 female mice and seven oocytes from nine male mice were retrieved. Immunocytochemical examinations of these oocytes after in vitro maturation revealed only two developed to the metaphase II stage. Most oocytes were between prophase and metaphase with abnormal microtubule organization and chromatin configuration. CONCLUSIONS: Immature oocytes in stored human ovarian tissue can grow to maturity in host animals after xenotransplantation. Retrieval of oocytes from the xenograft can be carried out and is reproducible. However, many oocytes, grown in host animals and further matured in vitro, showed aberrant microtubule organization and chromatin patterns.
- 1 October 2004
- Published by Elsevier in Fertility and Sterility
- Vol. 82 (4) , 930-932
Heterotopic autotransplantation of cryobanked human ovarian tissue as a strategy to restore ovarian function
- 1 October 2004
- Published by Elsevier in Fertility and Sterility
- Vol. 82 (4) , 930-932
Heterotopic autotransplantation of cryobanked human ovarian tissue as a strategy to restore ovarian function
- 1 September 2004
- Published by Elsevier in Fertility and Sterility
- Vol. 82 (3) , 679-685
Quantitative assessment of ischemic tissue damage in ovarian cortical tissue with or without antioxidant (ascorbic acid) treatment
- 1 September 2004
- Published by Elsevier in Fertility and Sterility
- Vol. 82 (3) , 679-685
Quantitative assessment of ischemic tissue damage in ovarian cortical tissue with or without antioxidant (ascorbic acid) treatment
- Open Access
- 1 September 2003
- Published by Oxford University Press (OUP) in Human Reproduction
- Vol. 18 (9) , 1759-1761
Ovarian tissue banking for cancer patients: To do or not to do?
A large proportion of childhood and young cancer patients will lose their fertility after aggressive cancer therapy because of the gonadotoxicities of chemotherapy and radiotherapy. One of the strategies to preserve fertility for those facing premature ovarian failure is ovarian tissue banking. We are seeing a growing enthusiasm about this emerging technology. At the same time, scepticism is prevalent, as the efficacy of ovarian tissue banking for fertility restoration in humans has not yet been proved. However, there is ample evidence of its efficacy in animal studies. Ovarian tissue banking requires further investigations and should be considered experimental in humans at present.
- 1 September 2003
- Published by Oxford University Press (OUP) in Human Reproduction
- Vol. 18 (9) , 1759-1761
Open AccessOvarian tissue banking for cancer patients: To do or not to do?
A large proportion of childhood and young cancer patients will lose their fertility after aggressive cancer therapy because of the gonadotoxicities of chemotherapy and radiotherapy. One of the strategies to preserve fertility for those facing premature ovarian failure is ovarian tissue banking. We are seeing a growing enthusiasm about this emerging technology. At the same time, scepticism is prevalent, as the efficacy of ovarian tissue banking for fertility restoration in humans has not yet been proved. However, there is ample evidence of its efficacy in animal studies. Ovarian tissue banking requires further investigations and should be considered experimental in humans at present.
- 1 July 2002
- Published by Elsevier in Fertility and Sterility
- Vol. 78 (1) , 77-82
Follicular development, ovulation, and corpus luteum formation in cryopreserved human ovarian tissue after xenotransplantation
- 1 July 2002
- Published by Elsevier in Fertility and Sterility
- Vol. 78 (1) , 77-82
Follicular development, ovulation, and corpus luteum formation in cryopreserved human ovarian tissue after xenotransplantation