Zobrazeno 1 - 10
of 782
pro vyhledávání: '"IHH"'
Publikováno v:
Healthcare Providers Industry Profile: Philippines. Mar2021, p1-35. 35p.
Autor:
Shimaa Medhat Abdellatif Ahmed, Nora ElSaid Badawi, Mohamed Ahmed AbdElSalam, Lubna Fawaz, AbdelKarim Kamel, Mona Mamdouh Hassan
Publikováno v:
Egyptian Pediatric Association Gazette, Vol 72, Iss 1, Pp 1-8 (2024)
Abstract Background Differentiation between isolated hypogonadotropic hypogonadism (IHH) and constitutional delay in puberty (CDP) throughout adolescence can be challenging for doctors. This study examines the withdrawal effects of short-term, low-do
Externí odkaz:
https://doaj.org/article/63492508c83a470ca34a244dbb2adbbd
Autor:
Archana Saikia, Hirendra Nath Sarma
Publikováno v:
Middle East Fertility Society Journal, Vol 29, Iss 1, Pp 1-10 (2024)
Abstract Indian hedgehog (Ihh) is a member of the developmentally regulated morphogens, the hedgehog gene family. The Hh protein family was initially discovered in Drosophila and has since been widely investigated in both Drosophila and higher animal
Externí odkaz:
https://doaj.org/article/832d5313693546d693f907a8ce88f806
Autor:
Mengtian Fan, Nana Geng, Xingyue Li, Danyang Yin, Yuyou Yang, Rong Jiang, Cheng Chen, Naibo Feng, Li Liang, Xiaoli Li, Fengtao Luo, Huabing Qi, Qiaoyan Tan, Yangli Xie, Fengjin Guo
Publikováno v:
Genes and Diseases, Vol 11, Iss 1, Pp 464-478 (2024)
Cartilage development is controlled by the highly synergistic proliferation and differentiation of growth plate chondrocytes, in which the Indian hedgehog (IHH) and parathyroid hormone-related protein-parathyroid hormone-1 receptor (PTHrP-PTH1R) feed
Externí odkaz:
https://doaj.org/article/0e9c70152c8f4b7cbfb4af286d8a2587
Publikováno v:
Acta Medica Lituanica, Vol 31, Iss 1 (2024)
Congenital abdominal adhesions are a rare condition that can result in a small bowel obstruction at any age, more frequently in pediatric populations. The cause remains unknown, and the importance of aberrant congenital bands is related to the diffic
Externí odkaz:
https://doaj.org/article/52d0a6cf5a46462a930bb55963a53f49
Publikováno v:
International Medical Case Reports Journal, Vol Volume 16, Pp 699-704 (2023)
Ying-Jie Ma,1,* Meng-Yao Li,1,2,* Jing-Yan Song,1,3 Zhen-Gao Sun1,3 1The First Clinical College, Shandong University of Traditional Chinese Medicine, Jinan, Shandong, People’s Republic of China; 2Department of Medical Oncology, Shuguang Hos
Externí odkaz:
https://doaj.org/article/ce3b53ce68da4becb605a46148421a47
Publikováno v:
Health Care Providers Industry Profile: Singapore. 6/ 1/2014, p1-31. 31p.
Publikováno v:
FRPT- M&A Snapshot. 12/2/2023, p1-1. 1/2p.
Autor:
Qian Cong, Yingzi Yang
Publikováno v:
Biomolecules, Vol 14, Iss 3, p 347 (2024)
Fibrodysplasia ossificans progressiva (FOP) is a rare congenital disorder characterized by abnormal bone formation due to ACVR1 gene mutations. The identification of the molecular mechanisms underlying the ectopic bone formation and expansion in FOP
Externí odkaz:
https://doaj.org/article/2072bb541e244ee8863ebf96991b11a5
Publikováno v:
FRPT- M&A Snapshot. 11/28/2023, p3-3. 2/3p.