Melita D. Irving: search on Z-Library

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1

All systems go: converging synthetic biology and combinatorial treatment for CAR-T cell therapy

Lanitis, Evripidis, Coukos, George, Irving, Melita

Journal:

Current Opinion in Biotechnology

Year:

2020

File:

PDF, 776 KB

2020

2

Infantile onset myofibrillar myopathy due to recessive CRYAB mutations

Katharine M.L. Forrest, Safa Al-Sarraj, Caroline Sewry, Stefan Buk, S. Veronica Tan, Matthew Pitt, Andrew Durward, Marilyn McDougall, Melita Irving, Michael G. Hanna, Emma Matthews, Anna Sarkozy, Judi

Journal:

Neuromuscular Disorders

Year:

2011

Language:

english

File:

PDF, 528 KB

english, 2011

3

Bisphosphonate therapy for spinal osteoporosis in Hajdu-Cheney syndrome – new data and literature review

Pittaway, James F. H., Harrison, Christopher, Rhee, Yumie, Holder-Espinasse, Muriel, Fryer, Alan E., Cundy, Tim, Drake, William M., Irving, Melita D.

Journal:

Orphanet Journal of Rare Diseases

Year:

2018

Language:

english

File:

PDF, 927 KB

english, 2018

4

Correction to: Bisphosphonate therapy for spinal osteoporosis in Hajdu-Cheney syndrome – new data and literature review

Pittaway, James F. H., Harrison, Christopher, Rhee, Yumie, Holder-Espinasse, Muriel, Fryer, Alan E., Cundy, Tim, Drake, William M., Irving, Melita D.

Journal:

Orphanet Journal of Rare Diseases

Year:

2019

Language:

english

File:

PDF, 256 KB

english, 2019

5

Best practice guidelines for management of spinal disorders in skeletal dysplasia

White, Klane K., Bober, Michael B., Cho, Tae-Joon, Goldberg, Michael J., Hoover-Fong, Julie, Irving, Melita, Kamps, Shawn E., Mackenzie, William G., Raggio, Cathleen, Spencer, Samantha A., Bompadre, V

Journal:

Orphanet Journal of Rare Diseases

Year:

2020

File:

PDF, 538 KB

2020

6

Deletion of the distal long arm of chromosome 10; is there a characteristic phenotype? A report of 15 de novo and familial cases

Melita Irving, Helen Hanson, Peter Turnpenny, Carole Brewer, Caroline Mackie Ogilvie, Angela Davies, Jonathan Berg

Journal:

American Journal of Medical Genetics Part A

Year:

2003

Language:

english

File:

PDF, 234 KB

english, 2003

7

Segmental paternal uniparental disomy (patUPD) of 14q32 with abnormal methylation elicits the characteristic features of complete patUPD14

Melita D. Irving, Karin Buiting, Deniz Kanber, Celia Donaghue, Reiner Schulz, Amaka Offiah, Shehla N. Mohammed, Rebecca J. Oakey

Journal:

American Journal of Medical Genetics Part A

Year:

2010

Language:

english

File:

PDF, 177 KB

english, 2010

8

Breast cancer genetics: Unsolved questions and open perspectives in an expanding clinical practice

Shirley V. Hodgson, Patrick J. Morrison, Melita Irving

Journal:

American Journal of Medical Genetics Part C: Seminars in Medical Genetics

Year:

2004

Language:

english

File:

PDF, 125 KB

english, 2004

9

Collagen VI glycine mutations: Perturbed assembly and a spectrum of clinical severity

Rishika A. Pace, Rachel A. Peat, Naomi L. Baker, Laura Zamurs, Matthias Mörgelin, Melita Irving, Naomi E. Adams, John F. Bateman, David Mowat, Nicholas J. C. Smith, Phillipa J. Lamont, Steven A. Moore

Journal:

Annals of Neurology

Year:

2008

Language:

english

File:

PDF, 937 KB

english, 2008

10

Random-peptide libraries and antigen-fragment libraries for epitope mapping and the development of vaccines and diagnostics

Melita B Irving, Oscar Pan, Jamie K Scott

Journal:

Current Opinion in Chemical Biology

Year:

2001

Language:

english

File:

PDF, 120 KB

english, 2001

11

Two Novel COL2A1 Mutations Associated with a Legg-Calvé-Perthes Disease-like Presentation

Peter Kannu, Melita Irving, Salim Aftimos, Ravi Savarirayan

Journal:

Clinical Orthopaedics and Related Research®

Year:

2011

Language:

english

File:

PDF, 260 KB

english, 2011

12

Clinical utility gene card for: 3M syndrome

Holder-Espinasse, Muriel, Irving, Melita, Cormier-Daire, Valérie

Journal:

European Journal of Human Genetics

Year:

2011

Language:

english

File:

PDF, 164 KB

english, 2011

13

Mutations in NOTCH2 cause Hajdu-Cheney syndrome, a disorder of severe and progressive bone loss

Simpson, Michael A, Irving, Melita D, Asilmaz, Esra, Gray, Mary J, Dafou, Dimitra, Elmslie, Frances V, Mansour, Sahar, Holder, Sue E, Brain, Caroline E, Burton, Barbara K

Journal:

Nature Genetics

Year:

2011

Language:

english

File:

PDF, 331 KB

english, 2011

14

Structure of a High-affinity “Mimotope” Peptide Bound to HIV-1-neutralizing Antibody b12 Explains its Inability to Elicit gp120 Cross-reactive Antibodies

Erica Ollmann Saphire, Marinieve Montero, Alfredo Menendez, Nienke E. van Houten, Melita B. Irving, Ralph Pantophlet, Michael B. Zwick, Paul W.H.I. Parren, Dennis R. Burton, Jamie K. Scott, Ian A. Wil

Journal:

Journal of Molecular Biology

Year:

2007

Language:

english

File:

PDF, 651 KB

english, 2007

15

Exploring peptide mimics for the production of antibodies against discontinuous protein epitopes

Melita B. Irving, Lisa Craig, Alfredo Menendez, Beechanahalli P. Gangadhar, Marinieve Montero, Nienke E. van Houten, Jamie K. Scott

Journal:

Molecular Immunology

Year:

2010

Language:

english

File:

PDF, 1014 KB

english, 2010

16

De Novo Mutations in MLL Cause Wiedemann-Steiner Syndrome

Wendy D. Jones, Dimitra Dafou, Meriel McEntagart, Wesley J. Woollard, Frances V. Elmslie, Muriel Holder-Espinasse, Melita Irving, Anand K. Saggar, Sarah Smithson, Richard C. Trembath, Charu Deshpande,

Journal:

The American Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 351 KB

english, 2012

17

Clinical Utility Gene Card for: 3-M syndrome - Update 2013

Holder-Espinasse, Muriel, Irving, Melita, Cormier-Daire, Valérie

Journal:

European Journal of Human Genetics

Year:

2014

Language:

english

File:

PDF, 190 KB

english, 2014

18

Possible association between complex congenital heart defects and 11p15 hypomethylation in three patients with severe Silver-Russell syndrome

Ghanim, Mustafa, Rossignol, Sylvie, Delobel, Bruno, Irving, Melita, Miller, Owen, Devisme, Louise, Plennevaux, Jean-Louis, Lucidarme-Rossi, Sophie, Manouvrier, Sylvie, Salah, Azzi, Chivu, Olimpia, Net

Journal:

American Journal of Medical Genetics Part A

Year:

2013

Language:

english

File:

PDF, 382 KB

english, 2013

19

Targeting the tumor vasculature to enhance T cell activity

Lanitis, Evripidis, Irving, Melita, Coukos, George

Journal:

Current Opinion in Immunology

Year:

2015

Language:

english

File:

PDF, 512 KB

english, 2015

20

Interplay between T Cell Receptor Binding Kinetics and the Level of Cognate Peptide Presented by Major Histocompatibility Complexes Governs CD8 + T Cell Responsiveness

Irving, Melita, Zoete, Vincent, Hebeisen, Michael, Schmid, Daphné, Baumgartner, Petra, Guillaume, Philippe, Romero, Pedro, Speiser, Daniel, Luescher, Immanuel, Rufer, Nathalie, Michielin, Olivier

Journal:

Journal of Biological Chemistry

Year:

2012

Language:

english

File:

PDF, 2.67 MB

english, 2012

21

Serpentine fibula polycystic kidney syndrome is part of the phenotypic spectrum of Hajdu–Cheney syndrome

Gray, Mary J, Kim, Chong Ae, Bertola, Debora Romeo, Arantes, Paula Ricci, Stewart, Helen, Simpson, Michael A, Irving, Melita D, Robertson, Stephen P

Journal:

European Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 226 KB

english, 2012

22

Chondrodysplasia punctata: a clinical diagnostic and radiological review

Irving, Melita D., Chitty, Lyn S., Mansour, Sahar, Hall, Christine M.

Journal:

Clinical Dysmorphology

Year:

2008

Language:

english

File:

PDF, 345 KB

english, 2008

23

Neonatal teeth in X-linked Opitz (G/BBB) syndrome

Shaw, Adam, Longman, Cheryl, Irving, Melita, Splitt, Miranda

Journal:

Clinical Dysmorphology

Year:

2006

Language:

english

File:

PDF, 73 KB

english, 2006

24

End-Stage Renal Disease in an Infant With Hajdu-Cheney Syndrome

Battelino, Nina, Writzl, Karin, Bratanič, Nevenka, Irving, Melita D, Novljan, Gregor

Journal:

Therapeutic Apheresis and Dialysis

Year:

2016

Language:

english

File:

PDF, 299 KB

english, 2016

25

1,2,3-Triazoles as inhibitors of indoleamine 2,3-dioxygenase 2 (IDO2)

Röhrig, Ute F., Majjigapu, Somi Reddy, Caldelari, Daniela, Dilek, Nahzli, Reichenbach, Patrick, Ascencao, Kelly, Irving, Melita, Coukos, George, Vogel, Pierre, Zoete, Vincent, Michielin, Olivier

Journal:

Bioorganic & Medicinal Chemistry Letters

Year:

2016

Language:

english

File:

PDF, 1.40 MB

english, 2016

26

De Novo Mutations in CHD4, an ATP-Dependent Chromatin Remodeler Gene, Cause an Intellectual Disability Syndrome with Distinctive Dysmorphisms

Weiss, Karin, Terhal, Paulien A., Cohen, Lior, Bruccoleri, Michael, Irving, Melita, Martinez, Ariel F., Rosenfeld, Jill A., Machol, Keren, Yang, Yaping, Liu, Pengfei, Walkiewicz, Magdalena, Beuten, Jo

Journal:

The American Journal of Human Genetics

Year:

2016

Language:

english

File:

PDF, 1.34 MB

english, 2016

27

Rodriguez acrofacial dysostosis is caused by apparently de novo heterozygous mutations in the SF3B4 gene

Irving, Melita D., Dimitrov, Boyan I., Wessels, Marja, Holder-Espinasse, Muriel, Chitayat, David, Simpson, Michael A.

Journal:

American Journal of Medical Genetics Part A

Year:

2016

Language:

english

File:

PDF, 858 KB

english, 2016

28

The T-Cell Receptor Can Bind to the Peptide-Bound Major Histocompatibility Complex and Uncomplexed Beta-2 Microglobulin through Distinct Binding Sites

Merkle, Patrick Sascha, Irving, Melita, Hongjian, Song, Ferber, Mathias, Jørgensen, Thomas J.D., Scholten, Kirsten, Luescher, Immanuel Florian, Coukos, George, Zoete, Vincent, Cuendet, Michel A., Mich

Journal:

Year:

2017

Language:

english

File:

PDF, 1.52 MB

english, 2017

29

Best practices in peri-operative management of patients with skeletal dysplasias

White, Klane K., Bompadre, Viviana, Goldberg, Michael J., Bober, Michael B., Cho, Tae-Joon, Hoover-Fong, Julie E., Irving, Melita, Mackenzie, William G., Kamps, Shawn E., Raggio, Cathleen, Redding, Gr

Journal:

American Journal of Medical Genetics Part A

Year:

2017

Language:

english

File:

PDF, 610 KB

english, 2017

30

In-Vivo Detection and Tracking of T Cells in Various Organs in a Melanoma Tumor Model by 19F-Fluorine MRS/MRI

Gonzales, Christine, Yoshihara, Hikari A. I., Dilek, Nahzli, Leignadier, Julie, Irving, Melita, Mieville, Pascal, Helm, Lothar, Michielin, Olivier, Schwitter, Juerg, Ryffel, Bernhard

Journal:

Year:

2016

Language:

english

File:

PDF, 2.05 MB

english, 2016

31

Engineering Chimeric Antigen Receptor T-Cells for Racing in Solid Tumors: Don’t Forget the Fuel

Irving, Melita, Vuillefroy de Silly, Romain, Scholten, Kirsten, Dilek, Nahzli, Coukos, George

Journal:

Frontiers in Immunology

Year:

2017

Language:

english

File:

PDF, 4.64 MB

english, 2017

32

Correction to: CART cells are prone to Fas- and DR5-mediated cell death

Tschumi, Benjamin O., Dumauthioz, Nina, Marti, Bastien, Zhang, Lianjun, Lanitis, Evripidis, Irving, Melita, Schneider, Pascal, Mach, Jean-Pierre, Coukos, George, Romero, Pedro, Donda, Alena

Journal:

Journal for ImmunoTherapy of Cancer

Year:

2018

Language:

english

File:

PDF, 138 KB

english, 2018

33

Best practice guidelines regarding prenatal evaluation and delivery of patients with skeletal dysplasia

Savarirayan, Ravi, Rossiter, Judith P., Hoover-Fong, Julie E., Irving, Melita, Bompadre, Viviana, Goldberg, Michael J., Bober, Michael B., Cho, Tae-Joon, Kamps, Shawn E., Mackenzie, William G., Raggio

Journal:

American Journal of Obstetrics and Gynecology

Year:

2018

Language:

english

File:

PDF, 423 KB

english, 2018

34

Depression Among Alcohol Consuming, HIV Positive Men on ART Treatment in India

Ha, Toan, Schensul, Stephen L., Irving, Mitchell, Brault, Marie A., Schensul, Jean J., Prabhughate, Priti, Vaz, Melita

Journal:

AIDS and Behavior

Year:

2018

File:

PDF, 862 KB

2018

35

Phenotypic presentations of Hajdu-Cheney syndrome according to age – 5 distinct clinical presentations

Graversen, Lise, Handrup, Mette Møller, Irving, Melita, Hove, Hanne, Diness, Birgitte Rode, Risom, Lotte, Svaneby, Dea, Aagaard, Mads Malik, Vogel, Ida, Gjørup, Hans, Davidsen, Michael, Hellfritzsch,

Journal:

European Journal of Medical Genetics

Year:

2019

Language:

english

File:

PDF, 3.27 MB

english, 2019

36

Phenotypic presentations of Hajdu-Cheney syndrome according to age – 5 distinct clinical presentations

Graversen, Lise, Handrup, Mette Møller, Irving, Melita, Hove, Hanne, Diness, Birgitte Rode, Risom, Lotte, Svaneby, Dea, Aagaard, Mads Malik, Vogel, Ida, Gjørup, Hans, Davidsen, Michael, Hellfritzsch,

Journal:

European Journal of Medical Genetics

Year:

2019

File:

PDF, 3.27 MB

2019

37

C-Type Natriuretic Peptide Analogue Therapy in Children with Achondroplasia

Savarirayan, Ravi, Irving, Melita, Bacino, Carlos A., Bostwick, Bret, Charrow, Joel, Cormier-Daire, Valerie, Le Quan Sang, Kim-Hanh, Dickson, Patricia, Harmatz, Paul, Phillips, John, Owen, Natalie, Ch

Journal:

New England Journal of Medicine

Year:

2019

Language:

english

File:

PDF, 373 KB

english, 2019

38

Rational combinations of immunotherapy with radiotherapy in ovarian cancer

Herrera, Fernanda G, Irving, Melita, Kandalaft, Lana E, Coukos, George

Journal:

The Lancet Oncology

Year:

2019

Language:

english

File:

PDF, 1.35 MB

english, 2019

39

The CHD4-related syndrome: a comprehensive investigation of the clinical spectrum, genotype–phenotype correlations, and molecular basis

Weiss, Karin, Lazar, Hayley P., Kurolap, Alina, Martinez, Ariel F., Paperna, Tamar, Cohen, Lior, Smeland, Marie F., Wallen, Sandra, Solveig, Heide, Keren, Boris, Terhal, Pauline, Irving, Melita, Takak

Journal:

Genetics in Medicine

Year:

2019

Language:

english

File:

PDF, 1.44 MB

english, 2019

40

CD8 binding of mhc-peptide complexes IN CIS or trans regulates CD8+ T cell responses

Liu, Yang, Cuendet, Michel A., Goffin, Laurence, Šachl, Radek, Cebecauer, Marek, Cariolato, Luca, Guillaume, Philippe, Reichenbach, Patrick, Irving, Melita, Coukos, George, Luescher, Immanuel F.

Journal:

Journal of Molecular Biology

Year:

2019

Language:

english

File:

PDF, 11.53 MB

english, 2019

41

Correction: The CHD4-related syndrome: a comprehensive investigation of the clinical spectrum, genotype–phenotype correlations, and molecular basis

Weiss, Karin, Lazar, Hayley P., Kurolap, Alina, Martinez, Ariel F., Paperna, Tamar, Cohen, Lior, Smeland, Marie F., Whalen, Sandra, Heide, Solveig, Keren, Boris, Terhal, Pauline, Irving, Melita, Takak

Journal:

Genetics in Medicine

Year:

2019

File:

PDF, 180 KB

2019

42

Preclinical Evaluation and Dosimetry of [111In]CHX-DTPA-scFv78-Fc Targeting Endosialin/Tumor Endothelial Marker 1 (TEM1)

Cicone, Francesco, DenoÃ«l, Thibaut, Gnesin, Silvano, Riggi, Nicolo, Irving, Melita, Jakka, Gopinadh, Schaefer, Niklaus, Viertl, David, Coukos, George, Prior, John O.

Journal:

Molecular Imaging and Biology

Year:

2020

Language:

english

File:

PDF, 1.94 MB

english, 2020

43

Correction to: Preclinical Evaluation and Dosimetry of [111In] CHX-DTPA-scFv78-Fc Targeting Endosialin/Tumor Endothelial Marker 1 (TEM1)

Cicone, Francesco, DenoÃ«l, Thibaut, Gnesin, Silvano, Riggi, Nicolo, Irving, Melita, Jakka, Gopinadh, Schaefer, Niklaus, Viertl, David, Coukos, George, Prior, John O.

Journal:

Molecular Imaging and Biology

Year:

2020

Language:

english

File:

PDF, 211 KB

english, 2020

44

Hip displacement in Wolf-Hirschhorn syndrome: Report on three cases and review of associated musculoskeletal pathologies

Buddhdev, Pranai K., Sabir, Ataf, Kokkinakis, Michailis, Irving, Melita, Norman-Taylor, Fabian

Journal:

American Journal of Medical Genetics Part A

Year:

2020

Language:

english

File:

PDF, 829 KB

english, 2020

45

SUN-093 Prospective Clinical Assessment Study in Children with Achondroplasia: The PROPEL Trial

Savarirayan, Ravi, Kannu, Peter, Dambkowski, Carl L, Rogoff, Daniela, Irving, Melita

Journal:

Journal of the Endocrine Society

Year:

2020

File:

PDF, 112 KB

2020

46

SAT-LB18 A Randomized Controlled Trial of Vosoritide in Children With Achondroplasia

Savarirayan, Ravi, Tofts, Louise, Irving, Melita, Wilcox, William, Bacino, Carlos A, Hoover-Fong, Julie, Font, Rosendo Ullot, Harmatz, Paul, Rutsch, Frank, Bober, Michael B, Polgreen, Lynda E, Ginebre

Journal:

Journal of the Endocrine Society

Year:

2020

File:

PDF, 95 KB

2020

47

Achondroplasia Foramen Magnum Score: screening infants for stenosis

Cheung, Moira S, Irving, Melita, Cocca, Alessandra, Santos, Rui, Shaunak, Meera, Dougherty, Harry, Siddiqui, Ata, Gringras, Paul, Thompson, Dominic

Journal:

Archives of Disease in Childhood

Year:

2020

File:

PDF, 843 KB

2020

48

Centrally mediated obstructive apnoea and restenosis of the foramen magnum in an infant with achondroplasia

Cocca, Alessandra, Thompson, Dominic, Rahim, Zehan, Irving, Melita, Farquhar, Michael, Santos, Rui, Cheung, Moira S.

Journal:

British Journal of Neurosurgery

Year:

2020

File:

PDF, 1.30 MB

2020

49

High versus low dose irradiation for tumor immune reprogramming

de Olza, Maria Ochoa, Bourhis, Jean, Irving, Melita, Coukos, George, Herrera, Fernanda G

Journal:

Current Opinion in Biotechnology

Year:

2020

File:

PDF, 2.97 MB

2020

50

Arthrogryposis as a presenting feature of nail-patella syndrome: a lesser-known feature and the perils of negative whole-genome sequencing

Sabir, Ataf H., Dermanis, Alexander A., Irving, Melita, Cheung, Moira

Journal:

Clinical Dysmorphology

Year:

2020

File:

PDF, 316 KB

2020