Hasil Pencarian - Mustafa K. Khokha
- Menampilkan 1 - 20 hasil dari 20
-
1
Breeding based remobilization of Tol2 transposon in Xenopus tropicalis. oleh Maura A Lane, Megan Kimber, Mustafa K Khokha
Diterbitkan 2013-01-01
Artikel -
2
-
3
Quantitative Phenotyping of Xenopus Embryonic Heart Pathophysiology Using Hemoglobin Contrast Subtraction Angiography to Screen Human Cardiomyopathies oleh Engin Deniz, Stephan Jonas, Mustafa K. Khokha, Mustafa K. Khokha, Michael A. Choma, Michael A. Choma, Michael A. Choma, Michael A. Choma
Diterbitkan 2019-09-01
Artikel -
4
-
5
-
6
Kap-β2/Transportin mediates β-catenin nuclear transport in Wnt signaling oleh Woong Y Hwang, Valentyna Kostiuk, Delfina P González, C Patrick Lusk, Mustafa K Khokha
Diterbitkan 2022-10-01
Artikel -
7
Cytotoxic T-Lymphocyte-Associated Protein 4 Haploinsufficiency-Associated Inflammation Can Occur Independently of T-Cell Hyperproliferation oleh Carole Le Coz, Brian E. Nolan, Melissa Trofa, Alicia M. Kamsheh, Mustafa K. Khokha, Mustafa K. Khokha, Mustafa K. Khokha, Saquib A. Lakhani, Saquib A. Lakhani, Antonio Novelli, Elaine H. Zackai, Elaine H. Zackai, Kathleen E. Sullivan, Kathleen E. Sullivan, Silvana Briuglia, Tricia R. Bhatti, Tricia R. Bhatti, Neil Romberg, Neil Romberg
Diterbitkan 2018-07-01
Artikel -
8
-
9
-
10
Identification of novel mutations and phenotype in the steroid resistant nephrotic syndrome gene NUP93: a case report oleh Ibrahim Sandokji, Jonathan Marquez, Weizhen Ji, Cynthia A. Zerillo, Monica Konstantino, Saquib A. Lakhani, Mustafa K. Khokha, Jillian K. Warejko
Diterbitkan 2019-07-01
Artikel -
11
Familial Dilated Cardiomyopathy Associated With a Novel Combination of Compound Heterozygous TNNC1 Variants oleh Maicon Landim-Vieira, Jamie R. Johnston, Weizhen Ji, Emily K. Mis, Joshua Tijerino, Michele Spencer-Manzon, Michele Spencer-Manzon, Lauren Jeffries, E. Kevin Hall, David Panisello-Manterola, Mustafa K. Khokha, Mustafa K. Khokha, Engin Deniz, P. Bryant Chase, Saquib A. Lakhani, Jose Renato Pinto
Diterbitkan 2020-01-01
Artikel -
12
Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development oleh Nick D.L. Owens, Ira L. Blitz, Maura A. Lane, Ilya Patrushev, John D. Overton, Michael J. Gilchrist, Ken W.Y. Cho, Mustafa K. Khokha
Diterbitkan 2016-01-01
Artikel -
13
CRISPR-Cpf1 mediates efficient homology-directed repair and temperature-controlled genome editing oleh Miguel A. Moreno-Mateos, Juan P. Fernandez, Romain Rouet, Charles E. Vejnar, Maura A. Lane, Emily Mis, Mustafa K. Khokha, Jennifer A. Doudna, Antonio J. Giraldez
Diterbitkan 2017-12-01
Artikel -
14
Author Correction: Membrane potential drives the exit from pluripotency and cell fate commitment via calcium and mTOR oleh Emily Sempou, Valentyna Kostiuk, Jie Zhu, M. Cecilia Guerra, Leonid Tyan, Woong Hwang, Elena Camacho-Aguilar, Michael J. Caplan, David Zenisek, Aryeh Warmflash, Nick D. L. Owens, Mustafa K. Khokha
Diterbitkan 2023-06-01
Artikel -
15
Membrane potential drives the exit from pluripotency and cell fate commitment via calcium and mTOR oleh Emily Sempou, Valentyna Kostiuk, Jie Zhu, M. Cecilia Guerra, Leonid Tyan, Woong Hwang, Elena Camacho-Aguilar, Michael J. Caplan, David Zenisek, Aryeh Warmflash, Nick D. L. Owens, Mustafa K. Khokha
Diterbitkan 2022-11-01
Artikel -
16
<i>SMC5</i> Plays Independent Roles in Congenital Heart Disease and Neurodevelopmental Disability oleh Matthew P. O’Brien, Marina V. Pryzhkova, Evelyn M. R. Lake, Francesca Mandino, Xilin Shen, Ruchika Karnik, Alisa Atkins, Michelle J. Xu, Weizhen Ji, Monica Konstantino, Martina Brueckner, Laura R. Ment, Mustafa K. Khokha, Philip W. Jordan
Diterbitkan 2023-12-01
Artikel -
17
A nonsense variant in Rap Guanine Nucleotide Exchange Factor 5 (RAPGEF5) is associated with equine familial isolated hypoparathyroidism in Thoroughbred foals. oleh Victor N Rivas, K Gary Magdesian, Sophia Fagan, Nathan M Slovis, Daniela Luethy, Laura H Javsicas, Brian G Caserto, Andrew D Miller, Anna R Dahlgren, Janel Peterson, Erin N Hales, Sichong Peng, Katherine D Watson, Mustafa K Khokha, Carrie J Finno
Diterbitkan 2020-09-01
Artikel -
18
AP2A2 mutation and defective endocytosis in a Malian family with hereditary spastic paraplegia oleh Salimata Diarra, Saikat Ghosh, Lassana Cissé, Thomas Coulibaly, Abdoulaye Yalcouyé, George Harmison, Salimata Diallo, Seybou H. Diallo, Oumar Coulibaly, Alice Schindler, Cheick A.K. Cissé, Alassane B. Maiga, Salia Bamba, Oumar Samassekou, Mustafa K. Khokha, Emily K. Mis, Saquib A. Lakhani, Frank X. Donovan, Steve Jacobson, Craig Blackstone, Cheick O. Guinto, Guida Landouré, Juan S. Bonifacino, Kenneth H. Fischbeck, Christopher Grunseich
Diterbitkan 2024-08-01
Artikel -
19
Genetic profile of progressive myoclonic epilepsy in Mali reveals novel findings oleh Lassana Cissé, Lassana Cissé, Salia Bamba, Salia Bamba, Seybou H. Diallo, Seybou H. Diallo, Weizhen Ji, Mohamed Emile Dembélé, Abdoulaye Yalcouyé, Abdoulaye Yalcouyé, Toumany Coulibaly, Ibrahima Traoré, Lauren Jeffries, Salimata Diarra, Salimata Diarra, Alassane Dit Baneye Maiga, Salimata Diallo, Karamoko Nimaga, Amadou Touré, Oumou Traoré, Mahamadou Kotioumbé, Emily Kathryn Mis, Cheick Abdel Kader Cissé, Cheick Oumar Guinto, Cheick Oumar Guinto, Kenneth H. Fischbeck, Mustafa K. Khokha, Saquib A. Lakhani, Guida Landouré, Guida Landouré
Diterbitkan 2024-09-01
Artikel -
20
Conserved chromatin and repetitive patterns reveal slow genome evolution in frogs oleh Jessen V. Bredeson, Austin B. Mudd, Sofia Medina-Ruiz, Therese Mitros, Owen Kabnick Smith, Kelly E. Miller, Jessica B. Lyons, Sanjit S. Batra, Joseph Park, Kodiak C. Berkoff, Christopher Plott, Jane Grimwood, Jeremy Schmutz, Guadalupe Aguirre-Figueroa, Mustafa K. Khokha, Maura Lane, Isabelle Philipp, Mara Laslo, James Hanken, Gwenneg Kerdivel, Nicolas Buisine, Laurent M. Sachs, Daniel R. Buchholz, Taejoon Kwon, Heidi Smith-Parker, Marcos Gridi-Papp, Michael J. Ryan, Robert D. Denton, John H. Malone, John B. Wallingford, Aaron F. Straight, Rebecca Heald, Dirk Hockemeyer, Richard M. Harland, Daniel S. Rokhsar
Diterbitkan 2024-01-01
Artikel