Results
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1301.
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Pulmonary veno-occlusive disease caused by an inherited mutation in bone morphogenetic protein receptor II. [electronic resource] by
- Runo, James R
- Vnencak-Jones, Cindy L
- Prince, Melissa
- Loyd, James E
- Wheeler, Lisa
- Robbins, Ivan M
- Lane, Kirk B
- Newman, John H
- Johnson, Joyce
- Nichols, William C
- Phillips, John A
Producer: 20030404
In:
American journal of respiratory and critical care medicine vol. 167
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1302.
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Endometrial and colorectal tumors from patients with hereditary nonpolyposis colon cancer display different patterns of microsatellite instability. [electronic resource] by
- Kuismanen, Shannon A
- Moisio, Anu-Liisa
- Schweizer, Pascal
- Truninger, Kaspar
- Salovaara, Reijo
- Arola, Johanna
- Butzow, Ralf
- Jiricny, Josef
- Nyström-Lahti, Minna
- Peltomäki, Päivi
Producer: 20020715
In:
The American journal of pathology vol. 160
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1303.
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1304.
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Down-regulation of epidermal growth factor receptor by selective expansion of a 5'-end regulatory dinucleotide repeat in colon cancer with microsatellite instability. [electronic resource] by
- Baranovskaya, Svetlana
- Martin, Yolanda
- Alonso, Sergio
- Pisarchuk, Ksenia L
- Falchetti, Mario
- Dai, Yuichi
- Khaldoyanidi, Sophia
- Krajewski, Stan
- Novikova, Inna
- Sidorenko, Yuri S
- Perucho, Manuel
- Malkhosyan, Sergei R
Producer: 20090928
In:
Clinical cancer research : an official journal of the American Association for Cancer Research vol. 15
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1305.
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1307.
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1308.
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Regulation of the major isoform of human endothelin-converting enzyme-1 by a strong housekeeping promoter modulated by polymorphic microsatellites. [electronic resource] by
- Funke-Kaiser, Heiko
- Thomas, Alexander
- Bremer, Juliane
- Kovacevic, Slobodan D
- Scheuch, Kathrin
- Bolbrinker, Juliane
- Theis, Steffen
- Lemmer, Julia
- Zimmermann, Andreas
- Zollmann, Frank S
- Herrmann, Stefan-Martin
- Paul, Martin
- Orzechowski, Hans-Dieter
Producer: 20040712
In:
Journal of hypertension vol. 21
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1309.
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1310.
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1311.
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1312.
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1313.
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1314.
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The gene encoding a cationic amino acid transporter (SLC7A4) maps to the region deleted in the velocardiofacial syndrome. [electronic resource] by
- Sperandeo, M P
- Borsani, G
- Incerti, B
- Zollo, M
- Rossi, E
- Zuffardi, O
- Castaldo, P
- Taglialatela, M
- Andria, G
- Sebastio, G
Producer: 19980806
In:
Genomics vol. 49
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1315.
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Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter. [electronic resource] by
- Simon, D B
- Nelson-Williams, C
- Bia, M J
- Ellison, D
- Karet, F E
- Molina, A M
- Vaara, I
- Iwata, F
- Cushner, H M
- Koolen, M
- Gainza, F J
- Gitleman, H J
- Lifton, R P
Producer: 19960201
In:
Nature genetics vol. 12
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1316.
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1317.
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Epidermal growth factor receptor intron-1 polymorphism predicts gefitinib outcome in advanced non-small cell lung cancer. [electronic resource] by
- Tiseo, Marcello
- Capelletti, Marzia
- De Palma, Giuseppe
- Franciosi, Vittorio
- Cavazzoni, Andrea
- Mozzoni, Paola
- Alfieri, Roberta R
- Goldoni, Matteo
- Galetti, Maricla
- Bortesi, Beatrice
- Bozzetti, Cecilia
- Loprevite, Maura
- Boni, Luca
- Camisa, Roberta
- Rindi, Guido
- Petronini, Pier Giorgio
- Ardizzoni, Andrea
Producer: 20090128
In:
Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer vol. 3
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1318.
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Association of the (CA)n repeat polymorphism of insulin-like growth factor-I and -202 A/C IGF-binding protein-3 promoter polymorphism with adult height in patients with severe growth hormone deficiency. [electronic resource] by
- Miletta, Maria Consolata
- Scheidegger, Ursina A
- Giordano, Mara
- Bozzola, Mauro
- Pagani, Sara
- Bona, Gianni
- Dattani, Mehul
- Hindmarsh, Peter C
- Petkovic, Vibor
- Oser-Meier, Monika
- Flück, Christa E
- Mullis, Primus-E
Producer: 20120823
In:
Clinical endocrinology vol. 76
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1319.
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