Results
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81.
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Anti-HER2 CD4(+) T-helper type 1 response is a novel immune correlate to pathologic response following neoadjuvant therapy in HER2-positive breast cancer. [electronic resource] by
- Datta, Jashodeep
- Berk, Erik
- Xu, Shuwen
- Fitzpatrick, Elizabeth
- Rosemblit, Cinthia
- Lowenfeld, Lea
- Goodman, Noah
- Lewis, David A
- Zhang, Paul J
- Fisher, Carla
- Roses, Robert E
- DeMichele, Angela
- Czerniecki, Brian J
Producer: 20160418
In:
Breast cancer research : BCR vol. 17
Availability: No items available.
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82.
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Deficiency of the two-pore-domain potassium channel TREK-1 promotes hyperoxia-induced lung injury. [electronic resource] by
- Schwingshackl, Andreas
- Teng, Bin
- Makena, Patrudu
- Ghosh, Manik
- Sinclair, Scott E
- Luellen, Charlean
- Balasz, Louisa
- Rovnaghi, Cynthia
- Bryan, Robert M
- Lloyd, Eric E
- Fitzpatrick, Elizabeth
- Saravia, Jordy S
- Cormier, Stephania A
- Waters, Christopher M
Producer: 20141215
In:
Critical care medicine vol. 42
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83.
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Addition of anti-estrogen therapy to anti-HER2 dendritic cell vaccination improves regional nodal immune response and pathologic complete response rate in patients with ER [electronic resource] by
- Lowenfeld, Lea
- Zaheer, Salman
- Oechsle, Crystal
- Fracol, Megan
- Datta, Jashodeep
- Xu, Shuwen
- Fitzpatrick, Elizabeth
- Roses, Robert E
- Fisher, Carla S
- McDonald, Elizabeth S
- Zhang, Paul J
- DeMichele, Angela
- Mick, Rosemarie
- Koski, Gary K
- Czerniecki, Brian J
Publication details: Oncoimmunology
In:
Oncoimmunology vol. 6
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84.
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Mutations in SH3PXD2B cause Borrone dermato-cardio-skeletal syndrome. [electronic resource] by
- Wilson, Gabrielle R
- Sunley, Jasmine
- Smith, Katherine R
- Pope, Kate
- Bromhead, Catherine J
- Fitzpatrick, Elizabeth
- Di Rocco, Maja
- van Steensel, Maurice
- Coman, David J
- Leventer, Richard J
- Delatycki, Martin B
- Amor, David J
- Bahlo, Melanie
- Lockhart, Paul J
Producer: 20150206
In:
European journal of human genetics : EJHG vol. 22
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85.
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Human and mouse mutations in WDR35 cause short-rib polydactyly syndromes due to abnormal ciliogenesis. [electronic resource] by
- Mill, Pleasantine
- Lockhart, Paul J
- Fitzpatrick, Elizabeth
- Mountford, Hayley S
- Hall, Emma A
- Reijns, Martin A M
- Keighren, Margaret
- Bahlo, Melanie
- Bromhead, Catherine J
- Budd, Peter
- Aftimos, Salim
- Delatycki, Martin B
- Savarirayan, Ravi
- Jackson, Ian J
- Amor, David J
Producer: 20110606
In:
American journal of human genetics vol. 88
Availability: No items available.
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86.
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Progressive loss of anti-HER2 CD4 [electronic resource] by
- Datta, Jashodeep
- Rosemblit, Cinthia
- Berk, Erik
- Showalter, Lori
- Namjoshi, Prachi
- Mick, Rosemarie
- Lee, Kathreen P
- Brod, Andrew M
- Yang, Rachel L
- Kelz, Rachel R
- Fitzpatrick, Elizabeth
- Hoyt, Clifford
- Feldman, Michael D
- Zhang, Paul J
- Xu, Shuwen
- Koski, Gary K
- Czerniecki, Brian J
Publication details: Oncoimmunology Oct 2015
In:
Oncoimmunology vol. 4
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87.
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Expanding the phenotypic spectrum of ARID1B-mediated disorders and identification of altered cell-cycle dynamics due to ARID1B haploinsufficiency. [electronic resource] by
- Sim, Joe C H
- White, Susan M
- Fitzpatrick, Elizabeth
- Wilson, Gabrielle R
- Gillies, Greta
- Pope, Kate
- Mountford, Hayley S
- Torring, Pernille M
- McKee, Shane
- Vulto-van Silfhout, Anneke T
- Jhangiani, Shalini N
- Muzny, Donna M
- Leventer, Richard J
- Delatycki, Martin B
- Amor, David J
- Lockhart, Paul J
Producer: 20140926
In:
Orphanet journal of rare diseases vol. 9
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88.
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A fibronectin scaffold approach to bispecific inhibitors of epidermal growth factor receptor and insulin-like growth factor-I receptor. [electronic resource] by
- Emanuel, Stuart L
- Engle, Linda J
- Chao, Ginger
- Zhu, Rong-Rong
- Cao, Carolyn
- Lin, Zheng
- Yamniuk, Aaron P
- Hosbach, Jennifer
- Brown, Jennifer
- Fitzpatrick, Elizabeth
- Gokemeijer, Jochem
- Morin, Paul
- Morse, Brent A
- Carvajal, Irvith M
- Fabrizio, David
- Wright, Martin C
- Das Gupta, Ruchira
- Gosselin, Michael
- Cataldo, Daniel
- Ryseck, Rolf P
- Doyle, Michael L
- Wong, Tai W
- Camphausen, Raymond T
- Cload, Sharon T
- Marsh, H Nicholas
- Gottardis, Marco M
- Furfine, Eric S
Producer: 20110725
In:
mAbs vol. 3
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89.
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Mutations in RAB39B cause X-linked intellectual disability and early-onset Parkinson disease with α-synuclein pathology. [electronic resource] by
- Wilson, Gabrielle R
- Sim, Joe C H
- McLean, Catriona
- Giannandrea, Maila
- Galea, Charles A
- Riseley, Jessica R
- Stephenson, Sarah E M
- Fitzpatrick, Elizabeth
- Haas, Stefan A
- Pope, Kate
- Hogan, Kirk J
- Gregg, Ronald G
- Bromhead, Catherine J
- Wargowski, David S
- Lawrence, Christopher H
- James, Paul A
- Churchyard, Andrew
- Gao, Yujing
- Phelan, Dean G
- Gillies, Greta
- Salce, Nicholas
- Stanford, Lynn
- Marsh, Ashley P L
- Mignogna, Maria L
- Hayflick, Susan J
- Leventer, Richard J
- Delatycki, Martin B
- Mellick, George D
- Kalscheuer, Vera M
- D'Adamo, Patrizia
- Bahlo, Melanie
- Amor, David J
- Lockhart, Paul J
Producer: 20150227
In:
American journal of human genetics vol. 95
Availability: No items available.
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