Bi-Hua Tan: search on Z-Library

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1

Sinus slowing caused by adenosine-5′-triphosphate in patients with and without sick sinus syndrome under various autonomic states

Bi-Hua Tan, Hiroki Shimizu, Yoshio Furukawa, Tetsuzou Kanemori, Mitsumasa Ohyanagi

Journal:

Journal of Electrocardiology

Year:

2004

Language:

english

File:

PDF, 84 KB

english, 2004

2

Wavelet transform analysis of heart rate variability to assess the autonomic changes associated with spontaneous coronary spasm of variant angina

Bi-Hua Tan, Hiroki Shimizu, Kenji Hiromoto, Yoshio Furukawa, Mitsumasa Ohyanagi, Tadaaki Iwasaki

Journal:

Journal of Electrocardiology

Year:

2003

Language:

english

File:

PDF, 175 KB

english, 2003

3

Gain-of-function mutation S422L in the KCNJ8-encoded cardiac KATP channel Kir6.1 as a pathogenic substrate for J-wave syndromes

Medeiros-Domingo, Argelia, Tan, Bi-Hua, Crotti, Lia, Tester, David J., Eckhardt, Lee, Cuoretti, Alessandra, Kroboth, Stacie L., Song, Chunhua, Zhou, Qing, Kopp, Doug, Schwartz, Peter J., Makielski, Jo

Journal:

Year:

2010

Language:

english

File:

PDF, 1.09 MB

english, 2010

4

Sudden infant death syndrome–associated mutations in the sodium channel beta subunits

Tan, Bi-Hua, Pundi, Kavitha N., Van Norstrand, David W., Valdivia, Carmen R., Tester, David J., Medeiros-Domingo, Argelia, Makielski, Jonathan C., Ackerman, Michael J.

Journal:

Year:

2010

Language:

english

File:

PDF, 1.64 MB

english, 2010

5

PARISIAN MEDICAL INTELLIGENCE.

Tan, Bi-Hua, Pundi, Kavitha N., Van Norstrand, David W., Valdivia, Carmen R., Tester, David J., Medeiros-Domingo, Argelia, Makielski, Jonathan C., Ackerman, Michael J.

Journal:

Year:

1861

Language:

english

File:

PDF, 400 KB

english, 1861

6

THE DALRYMPLE HOME FOR INEBRIATES: AN INTERESTING REPORT.

Tan, Bi-Hua, Valdivia, Carmen R., Ruwaldt, Karen M., Ye, Bin, Tester, David J., Ackerman, Michael J., Makielski, Jonathan C.

Journal:

Year:

1908

Language:

english

File:

PDF, 183 KB

english, 1908

7

Expression defects of the common polymorphisms S524Y and H558R in the Q1077 SCN5A variant can be rescued by mexiletine

Tan, Bi-Hua, Valdivia, Carmen R., Ruwaldt, Karen M., Ye, Bin, Tester, David J., Ackerman, Michael J., Makielski, Jonathan C.

Journal:

Year:

2005

Language:

english

File:

PDF, 66 KB

english, 2005

8

Functional Characterization of the Andersen-Tawil Syndrome Associated Mutation (M307I) in KCNJ2

Tan, Bi-Hua, Song, Chunhua, Kroboth, Stacie L., Zhou, Qing, Dovat, Sinisa, Ackerman, Michael J., Makielski, Janathan C., Eckhardt, Lee L.

Journal:

Biophysical Journal

Year:

2010

Language:

english

File:

PDF, 62 KB

english, 2010

9

Mutations in SNTA1 and SCN5A Interact to Increase Late Sodium Current in a Patient with Syncope

Hu, Roumu, Tan, Bi-Hua, Valdivia, Carmen, Orland, Kate M., Peterson, Amber, He, Yang, Park, Daniel J., Pu, Jielin, Makielski, Jonathan C.

Journal:

Biophysical Journal

Year:

2012

Language:

english

File:

PDF, 79 KB

english, 2012

10

SCN5A Missense Mutation from a Patient with Complex Cardiac Rhythm and Conduction Disorder Requires the Common Polymorphism H558R on the Same Allele for Arrhythmogenic Biophysical Phenotype

Tan, Bi-Hua, Medeiros, Argelia, Iturralde, Pedro, Ackerman, Michael J., Makielski, Jonathan C.

Journal:

Biophysical Journal

Year:

2009

Language:

english

File:

PDF, 40 KB

english, 2009

11

Common human SCN5A polymorphisms have altered electrophysiology when expressed in Q1077 splice variants

Tan, Bi-Hua, Valdivia, Carmen R., Rok, Benjamin A., Ye, Bin, Ruwaldt, Karen M., Tester, David J., Ackerman, Michael J., Makielski, Jonathan C.

Journal:

Year:

2005

Language:

english

File:

PDF, 324 KB

english, 2005

12

Reduced PIP2 Binding to KCNJ2 (M307I) Channels is Linked to Type 1 Andersen-Tawil Syndrome

Tan, Bi-Hua, Dovat, Sinisa, Peterson, Blaise Z., Song, Chunhua

Journal:

Biophysical Journal

Year:

2013

Language:

english

File:

PDF, 41 KB

english, 2013

13

AB16-3

Makielski, Jonathan C., Valdivia, Carmen R., Tan, Bi-Hua, Ueda, Kazuo, Kaku, Toshihiko, Ackerman, Michael J.

Journal:

Year:

2006

Language:

english

File:

PDF, 67 KB

english, 2006

14

Unique mixed phenotype and unexpected functional effect revealed by novel compound heterozygosity mutations involving SCN5A

Medeiros-Domingo, Argelia, Tan, Bi-Hua, Iturralde-Torres, Pedro, Tester, David J., Tusié-Luna, Teresa, Makielski, Jonathan C., Ackerman, Michael J.

Journal:

Year:

2009

Language:

english

File:

PDF, 1.52 MB

english, 2009

15

Trafficking-Defective Kir6.1 (KATP) Mutations in Sudden Infant Death Syndrome

Tan, Bi-Hua, Hu, Rou-Mu, Peterson, Blaise, Dovat, Sinisa, Ackerman, Michael J., Makielski, Jonathan C., Song, Chunhua

Journal:

Biophysical Journal

Year:

2014

Language:

english

File:

PDF, 144 KB

english, 2014

16

Arrhythmogenic Biophysical Phenotype for SCN5A Mutation S1787N Depends upon Splice Variant Background and Low pH

Tan, Bi-Hua, Song, Chunhua, Tester, David J., Zhou, Qing, He, Yang, Marion, Robert W., McDonald, Thomas V., Ackerman, Michael J., Makielski, Jonathan C.

Journal:

Biophysical Journal

Year:

2011

Language:

english

File:

PDF, 57 KB

english, 2011

17

The Brugada syndrome SCN5A mutation G1406R expression defect depends upon splice variant background Q1077 and is rescued by mexiletine

Tan, Bi-Hua, Valdivia, Carmen R., Makielski, Jonathan C.

Journal:

Year:

2005

Language:

english

File:

PDF, 95 KB

english, 2005

18

Sudden Unexplained Nocturnal Death Syndrome in Southern China

Cheng, Jianding, Makielski, Jonathan C., Yuan, Ping, Shi, Nianqing, Zhou, Feng, Ye, Bin, Tan, Bi-Hua, Kroboth, Stacie

Journal:

American Journal of Forensic Medicine & Pathology

Year:

2011

Language:

english

File:

PDF, 245 KB

english, 2011

19

Transcriptional Regulation of JARID1B/KDM5B Histone Demethylase by Ikaros, Histone Deacteylase 1 (HDAC1), and Casein Kinase 2 (CK2) in B Cell Acute Lymphoblastic Leukemia

Wang, Haijun, Song, Chunhua, Ding, Yali, Pan, Xiaokang, Ge, Zheng, Tan, Bi-Hua, Gowda, Chandrika, Sachdev, Mansi, Muthusami, Sunil, Ouyang, Hongsheng, Lai, Liangxue, Francis, Olivia L., Morris, Christ

Journal:

Journal of Biological Chemistry

Year:

2015

Language:

english

File:

PDF, 2.66 MB

english, 2015

20

Mechanisms Underlying the Loss-Of-Functional Kir6.1 KATP Channel Mutations in Sudden Infant Death Syndrome

Tan, Bi-Hua, Peterson, Blaise Z., Li, Ryan, Sun, Tianyu, Dovat, Sinisa, Ackerman, Michael J., Song, Chunhua

Journal:

Biophysical Journal

Year:

2015

Language:

english

File:

PDF, 43 KB

english, 2015

21

Loss-Of-Functional Kir6.1 KATP Channel Mutations Induce Cell Apoptosis through ROS Production and Mitochondrial Dysfunction

Tan, Bi-Hua, Xie, Shengyi, Sun, Tianyu, Dovat, Sinisa, Peterson, Blaise Z., Song, Chunhua

Journal:

Biophysical Journal

Year:

2016

Language:

english

File:

PDF, 51 KB

english, 2016

22

Dysfunction of Inward Rectifier Potassium Channel in Rbm20-/- Rats

Tan, Bi-Hua, Guo, Wei, Song, Chunhua, Greaser, Marion

Journal:

Biophysical Journal

Year:

2017

Language:

english

File:

PDF, 48 KB

english, 2017

23

Mexiletine rescues a mixed biophysical phenotype of the cardiac sodium channel arising from the SCN5A mutation, N406K, found in LQT3 patients

Hu, Rou-Mu, Tester, David J., Li, Ryan, Sun, Tianyu, Peterson, Blaise Z., Ackerman, Michael J., Makielski, Jonathan C., Tan, Bi-Hua

Journal:

Year:

2018

Language:

english

File:

PDF, 1.37 MB

english, 2018

24

LQTS-associated mutation A257G in α1-syntrophin interacts with the intragenic variant P74L to modify its biophysical phenotype

Cheng, Jianding, Van Norstrand, David W., Medeiros-Domingo, Argelia, Tester, David J., Valdivia, Carmen R., Tan, Bi-Hua, Vatta, Matteo, Makielski, Jonathan C., Ackerman, Michael J.

Journal:

Year:

2011

Language:

english

File:

PDF, 410 KB

english, 2011

25

Properties of a Stable and Sustained-Release Formulation of Recombinant Human Parathyroid Hormone (rhPTH) with Chitosan and Silk Fibroin Microparticles

Lv, Bi-Hua, Tan, Wei, Zhu, Chang-Cai, Shang, Xuejun, Zhang, Ling

Journal:

Medical Science Monitor

Year:

2018

Language:

english

File:

PDF, 962 KB

english, 2018

26

Evaluation of clinical effectiveness of paclitaxel and ursolic acid co-loaded liposomes as enhanced treatment for head and neck squamous cell carcinoma

Lv, Bi-Hua, Tan, Wei, Shang, Xuejun, Zhang, Ling

Journal:

Tropical Journal of Pharmaceutical Research

Year:

2019

File:

PDF, 590 KB

2019

27

A novel G6PD deleterious variant identified in three families with severe glucose-6-phosphate dehydrogenase deficiency

Tong, Yongqing, Liu, Bei, Zheng, Hongyun, Bao, Anyu, Wu, Zegang, Gu, Jian, Tan, Bi-Hua, McGrath, Mary, Kane, Shriya, Song, Chunhua, Li, Yan

Journal:

BMC Medical Genetics

Year:

2020

File:

PDF, 2.83 MB

2020

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