Amar J. Majmundar : rechercher sur Z-Library

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1

Combined millimeter wave and cyclophosphamide therapy of an experimental murine melanoma

Mahendra K. Logani, Ashok Bhanushali, Altaf Anga, Amar Majmundar, Imre Szabo, Marvin C. Ziskin

Journal:

Bioelectromagnetics

Année:

2004

Langue:

english

Fichier:

PDF, 298 KB

english, 2004

2

Hemodynamic and metabolic diffuse optical monitoring in a mouse model of hindlimb ischemia

Majmundar, Amar J., Simon, M. Celeste, Yodh, Arjun G., Mesquita, Rickson C., Skuli, Nicolas, Kim, Meeri N., Liang, Jiaming, Schenkel, Steve

Journal:

Biomedical Optics Express

Année:

2010

Langue:

english

Fichier:

PDF, 1.39 MB

english, 2010

3

Hypoxia-Inducible Factors and the Response to Hypoxic Stress

Amar J. Majmundar, Waihay J. Wong, M. Celeste Simon

Journal:

Année:

2010

Langue:

english

Fichier:

PDF, 761 KB

english, 2010

4

Epigenetic downregulation of the DNA repair gene MED1/MBD4 in colorectal and ovarian cancer

Howard, J. Harrison, Frolov, Andrey, Tzeng, Ching-Wei D., Stewart, Ashley, Midzak, Andrew, Majmundar, Amar, Godwin, Andrew, Heslin, Martin, Heslin, Martin, Bellacosa, Alfonso, Arnoletti, J. Pablo

Journal:

Cancer Biology & Therapy

Année:

2009

Fichier:

PDF, 517 KB

2009

5

Epigenetic downregulation of the DNA repair gene MED1/MBD4 in colorectal and ovarian cancer

Howard, J. Harrison, Frolov, Andrey, Tzeng, Ching-Wei D., Stewart, Ashley, Midzak, Andrew, Majmundar, Amar, Godwin, Andrew, Heslin, Martin, Heslin, Martin, Bellacosa, Alfonso, Arnoletti, J. Pablo

Journal:

Cancer Biology & Therapy

Année:

2009

Langue:

english

Fichier:

PDF, 517 KB

english, 2009

6

Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis

Daga, Ankana, Majmundar, Amar J., Braun, Daniela A., Gee, Heon Yung, Lawson, Jennifer A., Shril, Shirlee, Jobst-Schwan, Tilman, Vivante, Asaf, Schapiro, David, Tan, Weizhen, Warejko, Jillian K., Widme

Journal:

Kidney International

Année:

2017

Langue:

english

Fichier:

PDF, 948 KB

english, 2017

7

Genetic variants in the LAMA5 gene in pediatric nephrotic syndrome

Braun, Daniela A, Warejko, Jillian K, Ashraf, Shazia, Tan, Weizhen, Daga, Ankana, Schneider, Ronen, Hermle, Tobias, Jobst-Schwan, Tilman, Widmeier, Eugen, Majmundar, Amar J, Nakayama, Makiko, Schapiro

Journal:

Nephrology Dialysis Transplantation

Année:

2018

Langue:

english

Fichier:

PDF, 808 KB

english, 2018

8

Acute multi-sgRNA knockdown of KEOPS complex genes reproduces the microcephaly phenotype of the stable knockout zebrafish model

Jobst-Schwan, Tilman, Schmidt, Johanna Magdalena, Schneider, Ronen, Hoogstraten, Charlotte A., Ullmann, Jeremy F. P., Schapiro, David, Majmundar, Amar J., Kolb, Amy, Eddy, Kaitlyn, Shril, Shirlee, Bra

Journal:

Année:

2018

Langue:

english

Fichier:

PDF, 4.32 MB

english, 2018

9

Panel sequencing distinguishes monogenic forms of nephritis from nephrosis in children

Schapiro, David, Daga, Ankana, Lawson, Jennifer A, Majmundar, Amar J, Lovric, Svjetlana, Tan, Weizhen, Warejko, Jillian K, Fessi, Inés, Rao, Jia, Airik, Merlin, Gee, Heon Yung, Schneider, Ronen, Widme

Journal:

Nephrology Dialysis Transplantation

Année:

2018

Langue:

english

Fichier:

PDF, 268 KB

english, 2018

10

Mutations in WDR4 as a new cause of Galloway-Mowat syndrome

Braun, Daniela A., Shril, Shirlee, Sinha, Aditi, Schneider, Ronen, Tan, Weizhen, Ashraf, Shazia, Hermle, Tobias, Jobst-Schwan, Tilman, Widmeier, Eugen, Majmundar, Amar J., Daga, Ankana, Warejko, Jilli

Journal:

American Journal of Medical Genetics Part A

Année:

2018

Langue:

english

Fichier:

PDF, 1001 KB

english, 2018

11

Gene panel sequencing identifies a likely monogenic cause in 7% of 235 Pakistani families with nephrolithiasis

Amar, Ali, Majmundar, Amar J., Ullah, Ihsan, Afzal, Ayesha, Braun, Daniela A., Shril, Shirlee, Daga, Ankana, Jobst-Schwan, Tilman, Ahmad, Mumtaz, Sayer, John A., Gee, Heon Yung, Halbritter, Jan, Knöpf

Journal:

Année:

2019

Fichier:

PDF, 956 KB

2019

12

Corticosteroid treatment exacerbates nephrotic syndrome in a zebrafish model of magi2a knockout

Jobst-Schwan, Tilman, Hoogstraten, Charlotte A., Kolvenbach, Caroline M., Schmidt, Johanna Magdalena, Kolb, Amy, Eddy, Kaitlyn, Schneider, Ronen, Ashraf, Shazia, Widmeier, Eugen, Majmundar, Amar J., H

Journal:

Kidney International

Année:

2019

Fichier:

PDF, 2.86 MB

2019

13

Corticosteroid treatment exacerbates nephrotic syndrome in a zebrafish model of magi2a knockout

Jobst-Schwan, Tilman, Hoogstraten, Charlotte A., Kolvenbach, Caroline M., Schmidt, Johanna Magdalena, Kolb, Amy, Eddy, Kaitlyn, Schneider, Ronen, Ashraf, Shazia, Widmeier, Eugen, Majmundar, Amar J., H

Journal:

Kidney International

Année:

2019

Langue:

english

Fichier:

PDF, 2.86 MB

english, 2019

14

Mutations in KIRREL1, a slit diaphragm component, cause steroid-resistant nephrotic syndrome

Solanki, Ashish K., Widmeier, Eugen, Arif, Ehtesham, Sharma, Shailza, Daga, Ankana, Srivastava, Pankaj, Kwon, Sang-Ho, Hugo, Hannah, Nakayama, Makiko, Mann, Nina, Majmundar, Amar J., Tan, Wei, Gee, He

Journal:

Kidney International

Année:

2019

Langue:

english

Fichier:

PDF, 1.95 MB

english, 2019

15

CAKUT and Autonomic Dysfunction Caused by Acetylcholine Receptor Mutations

Mann, Nina, Kause, Franziska, Henze, Erik K., Gharpure, Anant, Shril, Shirlee, Connaughton, Dervla M., Nakayama, Makiko, Klämbt, Verena, Majmundar, Amar J., Wu, Chen-Han W., Kolvenbach, Caroline M., D

Journal:

The American Journal of Human Genetics

Année:

2019

Langue:

english

Fichier:

PDF, 996 KB

english, 2019

16

Mutations in transcription factor CP2-like 1 may cause a novel syndrome with distal renal tubulopathy in humans

KlÃ¤mbt, Verena, Werth, Max, Onuchic-Whitford, Ana C, Getwan, Maike, Kitzler, Thomas M, Buerger, Florian, Mao, Youying, Deutsch, Konstantin, Mann, Nina, Majmundar, Amar J, Kaminski, Michael M, Shen, T

Journal:

Nephrology Dialysis Transplantation

Année:

2020

Fichier:

PDF, 1010 KB

2020

17

DAAM2 Variants Cause Nephrotic Syndrome via Actin Dysregulation

Schneider, Ronen, Deutsch, Konstantin, Hoeprich, Gregory J., Marquez, Jonathan, Hermle, Tobias, Braun, Daniela A., Seltzsam, Steve, Kitzler, Thomas M., Mao, Youying, Buerger, Florian, Majmundar, Amar

Journal:

The American Journal of Human Genetics

Année:

2020

Fichier:

PDF, 175 KB

2020