Results
|
|
6501.
|
|
|
|
6502.
|
|
|
|
6503.
|
|
|
|
6504.
|
|
|
|
6505.
|
|
|
|
6506.
|
|
|
|
6507.
|
|
|
|
6508.
|
|
|
|
6509.
|
|
|
|
6510.
|
|
|
|
6511.
|
|
|
|
6512.
|
Fibroblast activation and abnormal extracellular matrix remodelling as common hallmarks in three cancer-prone genodermatoses. [electronic resource] by
- Chacón-Solano, E
- León, C
- Díaz, F
- García-García, F
- García, M
- Escámez, M J
- Guerrero-Aspizua, S
- Conti, C J
- Mencía, Á
- Martínez-Santamaría, L
- Llames, S
- Pévida, M
- Carbonell-Caballero, J
- Puig-Butillé, J A
- Maseda, R
- Puig, S
- de Lucas, R
- Baselga, E
- Larcher, F
- Dopazo, J
- Del Río, M
Producer: 20201221
In:
The British journal of dermatology vol. 181
Availability: No items available.
|
|
|
6513.
|
Two individuals with features of both xeroderma pigmentosum and trichothiodystrophy highlight the complexity of the clinical outcomes of mutations in the XPD gene. [electronic resource] by
- Broughton, B C
- Berneburg, M
- Fawcett, H
- Taylor, E M
- Arlett, C F
- Nardo, T
- Stefanini, M
- Menefee, E
- Price, V H
- Queille, S
- Sarasin, A
- Bohnert, E
- Krutmann, J
- Davidson, R
- Kraemer, K H
- Lehmann, A R
Producer: 20020221
In:
Human molecular genetics vol. 10
Availability: No items available.
|
|
|
6514.
|
Mutations in the selenocysteine insertion sequence-binding protein 2 gene lead to a multisystem selenoprotein deficiency disorder in humans. [electronic resource] by
- Schoenmakers, Erik
- Agostini, Maura
- Mitchell, Catherine
- Schoenmakers, Nadia
- Papp, Laura
- Rajanayagam, Odelia
- Padidela, Raja
- Ceron-Gutierrez, Lourdes
- Doffinger, Rainer
- Prevosto, Claudia
- Luan, Jian'an
- Montano, Sergio
- Lu, Jun
- Castanet, Mireille
- Clemons, Nick
- Groeneveld, Matthijs
- Castets, Perrine
- Karbaschi, Mahsa
- Aitken, Sri
- Dixon, Adrian
- Williams, Jane
- Campi, Irene
- Blount, Margaret
- Burton, Hannah
- Muntoni, Francesco
- O'Donovan, Dominic
- Dean, Andrew
- Warren, Anne
- Brierley, Charlotte
- Baguley, David
- Guicheney, Pascale
- Fitzgerald, Rebecca
- Coles, Alasdair
- Gaston, Hill
- Todd, Pamela
- Holmgren, Arne
- Khanna, Kum Kum
- Cooke, Marcus
- Semple, Robert
- Halsall, David
- Wareham, Nicholas
- Schwabe, John
- Grasso, Lucia
- Beck-Peccoz, Paolo
- Ogunko, Arthur
- Dattani, Mehul
- Gurnell, Mark
- Chatterjee, Krishna
Producer: 20110114
In:
The Journal of clinical investigation vol. 120
Availability: No items available.
|
|
|
6515.
|
|
|
|
6516.
|
|
|
|
6517.
|
|
|
|
6518.
|
|
|
|
6519.
|
|
|
|
6520.
|
Defective transcription-coupled repair in Cockayne syndrome B mice is associated with skin cancer predisposition. [electronic resource] by
- van der Horst, G T
- van Steeg, H
- Berg, R J
- van Gool, A J
- de Wit, J
- Weeda, G
- Morreau, H
- Beems, R B
- van Kreijl, C F
- de Gruijl, F R
- Bootsma, D
- Hoeijmakers, J H
Producer: 19970606
In:
Cell vol. 89
Availability: No items available.
|