日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Long-acting parathyroid hormone receptor agonist rectifies hypocalcemia in autosomal dominant hypocalcemia type 1 mice

长效甲状旁腺激素受体激动剂可纠正常染色体显性低钙血症1型小鼠的低钙血症。

Hannan, Fadil M; Stevenson, Mark; Elajnaf, Taha; Rostom, Hussam; Lines, Kate E; Stewart, Michelle; Wells, Sara; Moir, Lee; Gardella, Thomas J; Thakker, Rajesh V

Genetic variants predisposing to an increased risk of kidney stone disease.

导致肾结石疾病风险增加的基因变异

Lovegrove Catherine E, Goldsworthy Michelle, Haley Jeremy, Smelser Diane, Gorvin Caroline, Hannan Fadil M, Mahajan Anubha, Suri Mohnish, Sadeghi-Alavijeh Omid, Moochhala Shabbir H, Gale Daniel P, Carey David, Holmes Michael V, Furniss Dominic, Thakker Rajesh V, Howles Sarah A

Characterization of quinazolinone calcilytic therapy for autosomal dominant hypocalcemia type 1 (ADH1)

喹唑啉酮钙溶解疗法治疗常染色体显性低钙血症1型(ADH1)的特征分析

Hannan, Fadil M; Kooblall, Kreepa G; Stevenson, Mark; Elajnaf, Taha; Liu, Fangyu; Lines, Kate E; Meng, Xin; Stewart, Michelle; Wells, Sara; Nemeth, Edward F; Shoichet, Brian K; Kneissel, Michaela; Gasser, Juerg A; Thakker, Rajesh V

Cohort Profile for the Heat in Pregnancy- India (HiP-India) Study

印度妊娠期高温(HiP-India)研究的队列概况

Thiruvengadam, Ramachandran; Raghavan, Sreevatsan; Shanmugam, Rekha; Isaac, Tanya; Cipriano Flores, Gabriela De Jesus; Thonikund Sathishkumar, Arya; Bulla, Sudhakar Reddy; Dayal, Prakriti; Ayushi; Gosain, Mudita; Parmar, Neera; Kaur, Lovejeet; Arya, Divya; Singh, Savita; Misra, Sumit; Sharma, Dharmendra; Rattan, Taruna; Juyal, Mukesh; Nanda, Sunil Kumar; Daniel, Mary; Alaganandam, Padma; Jain, Rachna; Nigam, Prashanth; Pathak, Shantanu; Jones, Gabriel; Hannan, Fadil M; Desiraju, Koundinya; Sopory, Shailaja; Kshetrapal, Pallavi; Prabakaran, Stalin; Jogi, Sangeeta Raman; Devarsetty, Praveen; Singh, Alka; Vatish, Manu; Thilagnathan, Basky; Dey, Sagnik; Venugopal, Vidhya; Khurana, Ashok; Papageorghiou, Aris T; Jain, Yogesh; Woodward, Mark; Hirst, Jane E; Bhatnagar, Shinjini; Wadhwa, Nitya

GNAQ/GNA11 Mosaicism Is Associated with Abnormal Serum Calcium Indices and Microvascular Neurocalcification

GNAQ/GNA11嵌合体与血清钙指标异常和微血管神经钙化相关

Knöpfel, Nicole; Zecchin, Davide; Richardson, Hanna; Polubothu, Satyamaanasa; Barberan-Martin, Sara; Cullup, Thomas; Gholam, Karolina; Heales, Simon; Krywawych, Steve; López-Balboa, Pablo; Muwanga-Nanyonjo, Noreen; Ogunbiyi, Olumide; Puvirajasinghe, Clinda; Solman, Lea; Swarbrick, Katherine; Syed, Samira B; Tahir, Zubair; Tisdall, Martin M; Allgrove, Jeremy; Chesover, Alexander D; Aylett, Sarah E; Jacques, Thomas S; Hannan, Fadil M; Löbel, Ulrike; Semple, Robert K; Thakker, Rajesh V; Kinsler, Veronica A

GNAQ/GNA11 Mosaicism Causes Aberrant Calcium Signaling Susceptible to Targeted Therapeutics

GNAQ/GNA11嵌合体导致异常钙信号传导,这种异常钙信号传导对靶向治疗敏感

Davide Zecchin,Nicole Knöpfel,Anna K Gluck,Mark Stevenson,Aimie Sauvadet,Satyamaanasa Polubothu,Sara Barberan-Martin,Fanourios Michailidis,Dale Bryant,Asuka Inoue,Kate E Lines,Fadil M Hannan,Robert K Semple,Rajesh V Thakker,Veronica A Kinsler

Central Adiposity Increases Risk of Kidney Stone Disease through Effects on Serum Calcium Concentrations

中心性肥胖通过影响血清钙浓度增加肾结石风险

Lovegrove, Catherine E; Bešević, Jelena; Wiberg, Akira; Lacey, Ben; Littlejohns, Thomas J; Allen, Naomi E; Goldsworthy, Michelle; Kim, Jihye; Hannan, Fadil M; Curhan, Gary C; Turney, Ben W; McCarthy, Mark I; Mahajan, Anubha; Thakker, Rajesh V; Holmes, Michael V; Furniss, Dominic; Howles, Sarah A

GNA11 Variants Identified in Patients with Hypercalcemia or Hypocalcemia

在高钙血症或低钙血症患者中发现的 GNA11 变异

Sarah A Howles, Caroline M Gorvin, Treena Cranston, Angela Rogers, Anna K Gluck, Hannah Boon, Kate Gibson, Mushtaqur Rahman, Allen Root, M Andrew Nesbit, Fadil M Hannan, Rajesh V Thakker

Genome-Wide Mining of Selaginella moellendorffii for Hevein-like Lectins and Their Potential Molecular Mimicry with SARS-CoV-2 Spike Glycoprotein

利用卷柏基因组进行全基因组挖掘,寻找类橡胶蛋白凝集素及其与SARS-CoV-2刺突糖蛋白的潜在分子模拟作用

Alsolami, Ahmed; Dirar, Amina I; Konozy, Emadeldin Hassan E; Osman, Makarim El-Fadil M; Ibrahim, Mohanad A; Alshammari, Khalid Farhan; Alshammari, Fawwaz; Alazmi, Meshari; Said, Kamaleldin B

A Mouse Model with a Frameshift Mutation in the Nuclear Factor I/X (NFIX) Gene Has Phenotypic Features of Marshall-Smith Syndrome

核因子 I/X (NFIX) 基因移码突变的小鼠模型具有马歇尔-史密斯综合征的表型特征

Kooblall, Kreepa G; Stevenson, Mark; Stewart, Michelle; Harris, Lachlan; Zalucki, Oressia; Dewhurst, Hannah; Butterfield, Natalie; Leng, Houfu; Hough, Tertius A; Ma, Da; Siow, Bernard; Potter, Paul; Cox, Roger D; Brown, Stephen D M; Horwood, Nicole; Wright, Benjamin; Lockstone, Helen; Buck, David; Vincent, Tonia L; Hannan, Fadil M; Bassett, J H Duncan; Williams, Graham R; Lines, Kate E; Piper, Michael; Wells, Sara; Teboul, Lydia; Hennekam, Raoul C; Thakker, Rajesh V