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Showing results (461-470 of 482) with videos related to

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The Journal of Clinical Investigation|October 17, 2023
OSR1 disruption contributes to uterine factor infertility via impaired Müllerian duct development and endometrial receptivityAdriana Lofrano-Porto, Sidney Alcântara Pereira, Andrew Dauber, et al.
European Journal of Endocrinology|September 22, 2025
Natural history of nonfunctioning pituitary microadenomas: a systematic review and individual participant data meta-analysisVictor B Boesen, Tue H Hansen, Mohammad Motawea, et al.
The Journal of Clinical Endocrinology and Metabolism|March 22, 2017
Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious PubertyAndrew Dauber, Marina Cunha-Silva, Delanie B Macedo, et al.
Nature Reviews. Endocrinology|August 17, 2023
Pituitary adenoma or neuroendocrine tumour: the need for an integrated prognostic classificationKen K Y Ho, Ursula B Kaiser, Phillippe Chanson, et al.
Plos Biology|November 8, 2019
Hypothalamic miR-30 regulates puberty onset via repression of the puberty-suppressing factor, Mkrn3Violeta Heras, Susana Sangiao-Alvarellos, Maria Manfredi-Lozano, et al.
The New England Journal of Medicine|October 24, 2003
The GPR54 gene as a regulator of pubertyStephanie B Seminara, Sophie Messager, Emmanouella E Chatzidaki, et al.
The New England Journal of Medicine|June 7, 2013
Central precocious puberty caused by mutations in the imprinted gene MKRN3Ana Paula Abreu, Andrew Dauber, Delanie B Macedo, et al.
Molecular Cell|December 25, 2012
LSD2/KDM1B and its cofactor NPAC/GLYR1 endow a structural and molecular model for regulation of H3K4 demethylationRui Fang, Fei Chen, Zhenghong Dong, et al.
Cell|December 11, 2012
Tet3 CXXC domain and dioxygenase activity cooperatively regulate key genes for Xenopus eye and neural developmentYufei Xu, Chao Xu, Akiko Kato, et al.
The Journal of Clinical Endocrinology and Metabolism|September 2, 2011
GnRH-deficient phenotypes in humans and mice with heterozygous variants in KISS1/Kiss1Yee-Ming Chan, Sarabeth Broder-Fingert, Sophia Paraschos, et al.
Pageof 49

Showing results (461-470 of 482) with videos related to

Sort By:
Pageof 49
The Journal of Clinical Investigation|October 17, 2023
OSR1 disruption contributes to uterine factor infertility via impaired Müllerian duct development and endometrial receptivityAdriana Lofrano-Porto, Sidney Alcântara Pereira, Andrew Dauber, et al.
European Journal of Endocrinology|September 22, 2025
Natural history of nonfunctioning pituitary microadenomas: a systematic review and individual participant data meta-analysisVictor B Boesen, Tue H Hansen, Mohammad Motawea, et al.
The Journal of Clinical Endocrinology and Metabolism|March 22, 2017
Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious PubertyAndrew Dauber, Marina Cunha-Silva, Delanie B Macedo, et al.
Nature Reviews. Endocrinology|August 17, 2023
Pituitary adenoma or neuroendocrine tumour: the need for an integrated prognostic classificationKen K Y Ho, Ursula B Kaiser, Phillippe Chanson, et al.
Plos Biology|November 8, 2019
Hypothalamic miR-30 regulates puberty onset via repression of the puberty-suppressing factor, Mkrn3Violeta Heras, Susana Sangiao-Alvarellos, Maria Manfredi-Lozano, et al.
The New England Journal of Medicine|October 24, 2003
The GPR54 gene as a regulator of pubertyStephanie B Seminara, Sophie Messager, Emmanouella E Chatzidaki, et al.
The New England Journal of Medicine|June 7, 2013
Central precocious puberty caused by mutations in the imprinted gene MKRN3Ana Paula Abreu, Andrew Dauber, Delanie B Macedo, et al.
Molecular Cell|December 25, 2012
LSD2/KDM1B and its cofactor NPAC/GLYR1 endow a structural and molecular model for regulation of H3K4 demethylationRui Fang, Fei Chen, Zhenghong Dong, et al.
Cell|December 11, 2012
Tet3 CXXC domain and dioxygenase activity cooperatively regulate key genes for Xenopus eye and neural developmentYufei Xu, Chao Xu, Akiko Kato, et al.
The Journal of Clinical Endocrinology and Metabolism|September 2, 2011
GnRH-deficient phenotypes in humans and mice with heterozygous variants in KISS1/Kiss1Yee-Ming Chan, Sarabeth Broder-Fingert, Sophia Paraschos, et al.
Pageof 49