The Manton Center for Orphan Disease Research
January 2011 - April 2011
A novel gene required for male fertility and functional CATSPER channel formation in spermatozoa.
Chung, J-J, Navarro, B, Krapivinsky, G, Krapivinsky, L, and Clapham, DE. 2011.
1] Howard Hughes Medical Institute, Manton Center for Orphan Disease, Children's Hospital, Boston, Massachusetts 02115, USA..  Department of Neurobiology, Harvard Medical School, Enders 1309, 320 Longwood Avenue, Boston, Massachusetts 02115, USA.
Myotubularin controls desmin intermediate filament architecture and mitochondrial dynamics in human and mouse skeletal muscle.
Hnia K, Tronchère H, Tomczak KK, Amoasii L, Schultz P, Beggs AH, Payrastre B, Mandel JL, Laporte J.
Department of Neurobiology and Genetics, Institut de Génétique et de Biologie Moléculaire et Cellulaire, Illkirch, France.
Novel mutations in NEB cause abnormal nebulin expression and markedly impaired muscle force generation in severe nemaline myopathy.
Lawlor MW, Ottenheijm CA, Lehtokari V-L, Cho K, Pelin K, Wallgren-Pettersson C, Granzier H, Beggs AH.
Division of Genetics and Program in Genomics, The Manton Center for Orphan Disease Research, Boston Children's Hospital, Harvard Medical School, 300 Longwood Avenue, CLSB 15026, Boston, MA 02115, USA. email@example.com.
Gene therapy for primary immunodeficiencies: Looking ahead, toward gene correction.
Pessach IM, Notarangelo LD.
Department of Pediatric Critical Care and Talpiot Medical Leadership Program, Safra Children's Hospital, Sheba Medical Center, Tel-Hashomer, Israel.
Structural grading of foveal hypoplasia using spectral domain optical coherence tomography: A predictor of visual acuity?
Thomas MG, Kumar A, Proudlock FA, Engle EC, Andrews C, Chan W-M, Thomas S, Gottlob, I.
Ophthalmology Group, School of Medicine, University of Leicester, Leicester, United Kingdom.
Two novel CHN1 mutations in two families with Duane's retraction syndrome.
Chan W-M, Miyake N, Zhu-Tam L, Andrews C, Engle EC.
Department of Neurology, Boston Children's Hospital, 300 Longwood Ave, Boston, MA 02115, USA.
Inhibition of activin receptor type IIB increases strength and lifespan in myotubularin-deficient mice.
Lawlor MW, Read BP, Edelstein R, Yang N, Pierson CR, Stein MJ, Wermer-Colan A, Buj-Bello A, Lachey JL, Seehra JS, Beggs AH.
Division of Genetics and Program in Genomics, The Manton Center for Orphan Disease Research, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Ultra fast and sensitive liquid chromatography andem mass spectrometry based assay for galactose-1-phosphate uridylyltransferase and galactokinase deficiencies.
Li Y, Ptolemy AS, Harmonay L, Kellogg M, Berry GT.
The Manton Center for Orphan Disease Research, Division of Genetics, Department of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
A 9-month-old boy with seizures and discrepant urine tryptophan concentrations.
Ptolemy AS, Li Y, Sanderson T, Khwaja O, Berry GT, Kellogg M.
Department of Laboratory Medicine, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA. firstname.lastname@example.org.
Tet1 and Tet2 regulate 5-hydroxymethylcytosine production and cell lineage specification in mouse embryonic stem cells.
Koh KP, Yabuuchi A, Rao S, Huang Y, Cunniff K, Nardone J, Laiho A, Tahiliani M, Sommer CA, Mostoslavsky G, Lahesmaa R, Orkin SH, Rodig SJ, Daley GQ, Rao A.
Immune Disease Institute and Program in Cellular and Molecular Medicine, Boston Children's Hospital, Boston, MA 02115, USA.
Cellular therapy for fanconi anemia: the past, present, and future.
MacMillan ML, Hughes MR, Agarwal S, Daley GQ.
The Division of Pediatric Hematology, Oncology, and Blood and Marrow Transplantation, University of Minnesota Blood and Marrow Transplant Program, Minneapolis, Minnesota, USA. email@example.com.
Stage-specific signaling through TGFβ family members and WNT regulates patterning and pancreatic specification of human pluripotent stem cells.
Nostro MC, Sarangi F, Ogawa S, Holtzinger A, Corneo B, Li X, Micallef SJ, Park IH, Basford C, Wheeler MB, Daley GQ, Elefanty AG, Stanley EG, Keller G.
McEwen Centre for Regenerative Medicine, University Health Network, Toronto, Ontario, Canada.
Hematopoietic differentiation of induced pluripotent stem cells from patients with mucopolysaccharidosis type I (Hurler syndrome).
Tolar J, Park IH, Xia L, Lees CJ, Peacock B, Webber B, McElmurry RT, Eide CR, Orchard PJ, Kyba M, Osborn MJ, Lund TC, Wagner JE, Daley GQ, Blazar BR.
Division of Hematology-Oncology, Blood and Marrow Transplantation, Department of Pediatrics, University of MN, Minneapolis, MN, USA. firstname.lastname@example.org.
Transplantation of Adult Mouse iPS Cell-Derived Photoreceptor Precursors Restores Retinal Structure and Function in Degenerative Mice.
Tucker BA, Park IH, Qi SD, Klassen HJ, Jiang C, Yao J, Redenti S, Daley GQ, Young MJ.
Department of Ophthalmology, Institute for Vision Research, Carver College of Medicine, University of Iowa, Iowa City, Iowa, United States of America. email@example.com.
Induced pluripotent stem cells for neural tissue engineering.
Wang A, Tang Z, Park IH, Zhu Y, Patel S, Daley GQ, Li S.
Department of Bioengineering, University of California, Berkeley, B108A Stanley Hall, Berkeley, CA 94720-1762, USA.
Investigating monogenic and complex diseases with pluripotent stem cells.
Zhu H, Lensch MW, Cahan P, Daley GQ.
Division of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts 02115, USA.
Congenital Microcephaly with a Simplified Gyral Pattern: Associated Findings and Their Significance.
Adachi Y, Poduri A, Kawaguch A, Yoon G, Salih MA, Yamashita F, Walsh CA, Barkovich AJ.
Department of Radiology and Biomedical Imaging, University of California, San Francisco, San Francisco, California.
Human Mutations in NDE1 Cause Extreme Microcephaly with Lissencephaly.
Alkuraya FS, Cai X, Emery C, Mochida GH, Al-Dosari MS, Felie JM, Hill RS, Barry BJ, Partlow JN, Gascon GG, Kentab A, Jan M, Shaheen R, Feng Y, Walsh CA.
Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh 11211, Saudi Arabia.
A forward genetic screen with a thalamocortical axon reporter mouse yields novel neurodevelopment mutants and a distinct emx2 mutant phenotype.
Dwyer ND, Manning DK, Moran JL, Mudbhary R, Fleming MS, Favero CB, Vock VM, O'Leary DD, Walsh CA, Beier DR.
Howard Hughes Medical Institute, Department of Neurology, Beth Israel Deaconess Medical Center, Boston, MA, USA. firstname.lastname@example.org.
The cerebrospinal fluid provides a proliferative niche for neural progenitor cells.
Lehtinen MK, Zappaterra MW, Chen X, Yang YJ, Hill AD, Lun M, Maynard T, Gonzalez D, Kim S, Ye P, D'Ercole AJ, Wong ET, Lamantia AS, Walsh CA.
Division of Genetics, Howard Hughes Medical Institute, Boston Children's Hospital, Boston, MA 02115, USA.
Loss-of-function mutations in PTPN11 cause metachondromatosis, but not Ollier disease or Maffucci syndrome.
Bowen ME, Boyden ED, Holm IA, Campos-Xavier B, Bonafé L, Superti-Furga A, Ikegawa S, Cormier-Daire V, Bovée JV, Pansuriya TC, de Sousa SB, Savarirayan R, Andreucci E, Vikkula M, Garavelli L, Pottinger C, Ogino T, Sakai A, Regazzoni BM, Wuyts W, Sangiorgi L, Pedrini E, Zhu M, Kozakewich HP, Kasser JR, Seidman JG, Kurek KC, Warman ML.
Department of Orthopaedic Surgery, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts, United States of America.
Gene expression profiling of skeletal muscles treated with a soluble activin type IIB receptor.
Rahimov F, King OD, Warsing LC, Powell RE, Emerson CP Jr, Kunkel LM, Wagner KR.
Program in Genomics, Division of Genetics, Boston Children's Hospital, Harvard Medical School, Boston, USA.
TRPM7, the Mg(2+) Inhibited Channel and Kinase.
Bates-Withers C, Sah R, Clapham DE.
Department of Cardiology, Howard Hughes Medical Institute, Manton Center for Orphan Disease, Boston Children's Hospital, 02115 Boston, MA, USA. email@example.com.
Resveratrol Inhibits Pathological Retinal Neovascularization in Vldlr-/- Mice.
Hua J, Guerin KI, ChenJ, Michan S, Stahl A, Krah NM, Seaward MR, Dennison RJ, Juan AM, Hatton CJ, Sapieha P, Sinclair D, Smith LE.
Department of Ophthalmology, Harvard Medical School, Children's Hospital, Boston, Massachusetts 02115, USA.