Up a level
Export as [feed] Atom [feed] RSS 1.0 [feed] RSS 2.0
Group by: Item Type | Date | No Grouping
Number of items: 10.

Journal Article

Chen, Jing, Isachenko, Evgenia, Wang, Wanxue, Du, Xinxin, Wang, Mengying, Rahimi, Gohar, Mallmann, Peter and Isachenko, Vladimir ORCID: 0000-0002-3674-543X . Optimization of Follicle Isolation for Bioengineering of Human Artificial Ovary. Biopreserv. Biobank.. NEW ROCHELLE: MARY ANN LIEBERT, INC. ISSN 1947-5543

Chen, Jing ORCID: 0000-0003-0538-689X, Liao, Hai-Jun, Xie, Hai-Dong, Han, Xing-Jie, Huang, Rui-Zhen, Cheng, Song, Wei, Zhong-Chao, Xie, Zhi-Yuan and Xiang, Tao ORCID: 0000-0001-5998-7338 (2017). Phase Transition of the q-State Clock Model: Duality and Tensor Renormalization. Chin. Phys. Lett., 34 (5). BRISTOL: IOP PUBLISHING LTD. ISSN 1741-3540

Chen, Jing ORCID: 0000-0001-8923-9971, Todorov, Plamen ORCID: 0000-0003-3731-6116, Isachenko, Evgenia, Rahimi, Gohar, Mallmann, Peter and Isachenko, Vladimir ORCID: 0000-0002-3674-543X . Construction and cryopreservation of an artificial ovary in cancer patients as an element of cancer therapy and a promising approach to fertility restoration. Hum. Fertil.. ABINGDON: TAYLOR & FRANCIS LTD. ISSN 1742-8149

Kohl, Stefan, Chen, Jing, Vivante, Asaf, Hwang, Daw-Yang, Shril, Shirlee, Dworschak, Gabriel C., Van der Ven, Amelie, Sanna-Cherchi, Simone, Bauer, Stuart B., Lee, Richard S., Soliman, Neveen A., Kehinde, Elijah O., Reutter, Heiko M., Tasic, Velibor ORCID: 0000-0002-3377-1245 and Hildebrandt, Friedhelm (2016). Targeted sequencing of 96 renal developmental microRNAs in 1213 individuals from 980 families with congenital anomalies of the kidney and urinary tract. Nephrol. Dial. Transplant., 31 (8). S. 1280 - 1284. OXFORD: OXFORD UNIV PRESS. ISSN 1460-2385

Li, Jianhua, Chen, Jing, Sun, Tiecheng, Zhang, Shuiwen, Jiao, Tingting, Chian, Ri-Cheng, Li, Youzhu and Xu, Ye ORCID: 0000-0003-4649-3624 (2021). Chromosome aneuploidy analysis in embryos derived from in vivo and in vitro matured human oocytes. J. Transl. Med., 19 (1). LONDON: BMC. ISSN 1479-5876

Liang, Lei, Mei, Libin, Shi, Yingying, Huang, Lingling, Su, Zhiying, Zeng, Yu, Gao, Haijie, He, Xuemei, Huang, Hui, Huang, Yanru, Li, Ping and Chen, Jing (2021). Turner syndrome with Xp deletions and rare endometrial abnormalities A case report. Medicine (Baltimore), 100 (46). PHILADELPHIA: LIPPINCOTT WILLIAMS & WILKINS. ISSN 1536-5964

Sha, Yanwei, Liu, Wensheng, Li, Lin, Serafimovski, Mario, Isachenko, Vladimir, Li, Youzhu, Chen, Jing, Zhao, Bangrong, Wang, Yifeng and Wei, Xiaoli (2021). Pathogenic Variants in ACTRT1 Cause Acephalic Spermatozoa Syndrome. Front. Cell. Dev. Biol., 9. LAUSANNE: FRONTIERS MEDIA SA. ISSN 2296-634X

Vivante, Asaf, Hwang, Daw-Yang, Kohl, Stefan, Chen, Jing, Shril, Shirlee, Schulz, Julian, van der Ven, Annelle, Daouk, Ghaleb, Soliman, Neveen A., Kumar, Aravind Selvin, Senguttuvan, Prabha, Kehinde, Elijah O., Tasic, Velibor ORCID: 0000-0002-3377-1245 and Hildebrandt, Friedhelm (2017). Exome Sequencing Discerns Syndromes in Patients from Consanguineous Families with Congenital Anomalies of the Kidneys and Urinary Tract. J. Am. Soc. Nephrol., 28 (1). S. 69 - 76. WASHINGTON: AMER SOC NEPHROLOGY. ISSN 1533-3450

Wei, Xiaoli, Liu, Wensheng, Zhu, Xingshen, Li, Youzhu, Zhang, Xiaoya, Chen, Jing, Isachenko, Vladimir, Sha, Yanwei and Lu, Zhongxian (2021). Biallelic mutations in KATNAL2 cause male infertility due to oligo-astheno-teratozoospermia. Clin. Genet., 100 (4). S. 376 - 386. HOBOKEN: WILEY. ISSN 1399-0004

van der Ven, Amelie T., Kobbe, Birgit, Kohl, Stefan, Shril, Shirlee, Pogoda, Hans-Martin, Imhof, Thomas, Ityel, Hadas, Vivante, Asaf, Chen, Jing, Hwang, Daw-Yang, Connaughton, Dervla M., Mann, Nina, Widmeier, Eugen ORCID: 0000-0002-7773-5190, Taglienti, Mary, Schmidt, Johanna Magdalena, Nakayama, Makiko, Senguttuvan, Prabha, Kumar, Selvin, Tasic, Velibor ORCID: 0000-0002-3377-1245, Kehinde, Elijah O., Mane, Shrikant M., Lifton, Richard P., Soliman, Neveen ORCID: 0000-0002-8942-1973, Lu, Weining ORCID: 0000-0002-6570-3044, Bauer, Stuart B., Hammerschmidt, Matthias, Wagener, Raimund and Hildebrandt, Friedhelm (2018). A homozygous missense variant in VWA2, encoding an interactor of the Fraser-complex, in a patient with vesicoureteral refluxy. PLoS One, 13 (1). SAN FRANCISCO: PUBLIC LIBRARY SCIENCE. ISSN 1932-6203

This list was generated on Mon May 23 05:48:49 2022 CEST.