Results
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3921.
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Germline variation in the oxidative DNA repair genes NUDT1 and OGG1 is not associated with hereditary colorectal cancer or polyposis. [electronic resource] by
- Mur, Pilar
- Jemth, Ann-Sofie
- Bevc, Luka
- Amaral, Nuno
- Navarro, Matilde
- Valdés-Mas, Rafael
- Pons, Tirso
- Aiza, Gemma
- Urioste, Miguel
- Valencia, Alfonso
- Lázaro, Conxi
- Moreno, Victor
- Puente, Xose S
- Stenmark, Pål
- Warpman-Berglund, Ulrika
- Capellá, Gabriel
- Helleday, Thomas
- Valle, Laura
Producer: 20190726
In:
Human mutation vol. 39
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3922.
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SNP association study in PMS2-associated Lynch syndrome. [electronic resource] by
- Ten Broeke, Sanne W
- Elsayed, Fadwa A
- Pagan, Lisa
- Olderode-Berends, Maran J W
- Garcia, Encarna Gomez
- Gille, Hans J P
- van Hest, Liselot P
- Letteboer, Tom G W
- van der Kolk, Lizet E
- Mensenkamp, Arjen R
- van Os, Theo A
- Spruijt, Liesbeth
- Redeker, Bert J W
- Suerink, Manon
- Vos, Yvonne J
- Wagner, Anja
- Wijnen, Juul T
- Steyerberg, E W
- Tops, Carli M J
- van Wezel, Tom
- Nielsen, Maartje
Producer: 20190305
In:
Familial cancer vol. 17
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3923.
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3924.
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3925.
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3926.
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3927.
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Four novel MSH2 / MLH1 gene mutations in portuguese HNPCC families. [electronic resource] by
- Isidro, G
- Veiga, I
- Matos, P
- Almeida, S
- Bizarro, S
- Marshall, B
- Baptista, M
- Leite, J
- Regateiro, F
- Soares, J
- Castedo, S
- Boavida, M G
Producer: 20000120
In:
Human mutation vol. 15
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3928.
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3929.
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3930.
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3931.
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Genomic rearrangements in MSH2 and MLH1 are rare mutational events in Spanish patients with hereditary nonpolyposis colorectal cancer. [electronic resource] by
- Castellví-Bel, Sergi
- Castells, Antoni
- Strunk, Mark
- Ferrández, Angel
- Piazuelo, Elena
- Milà, Montserrat
- Piñol, Virgínia
- Rodríguez-Moranta, Francisco
- Andreu, Montserrat
- Lanas, Angel
- Piqué, Josep Maria
Producer: 20050721
In:
Cancer letters vol. 225
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3932.
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Clinicopathological and molecular genetic analysis of HNPCC in China. [electronic resource] by
- Luo, Ding-Cun
- Cai, Qi
- Sun, Meng-Hong
- Ni, Yao-Zhong
- Ni, Shi-Chang
- Chen, Zhe-Jing
- Li, Xiao-Yang
- Tao, Chong-Wei
- Zhang, Xue-Miao
- Shi, Da-Ren
Producer: 20050511
In:
World journal of gastroenterology vol. 11
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3933.
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3934.
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Germline hypermethylation of MLH1 and EPCAM deletions are a frequent cause of Lynch syndrome. [electronic resource] by
- Niessen, Renée C
- Hofstra, Robert M W
- Westers, Helga
- Ligtenberg, Marjolijn J L
- Kooi, Krista
- Jager, Paul O J
- de Groote, Marloes L
- Dijkhuizen, Trijnie
- Olderode-Berends, Maran J W
- Hollema, Harry
- Kleibeuker, Jan H
- Sijmons, Rolf H
Producer: 20090909
In:
Genes, chromosomes & cancer vol. 48
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3935.
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3936.
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Lymphocyte-rich renal cell carcinoma: an unusual histomorphologic manifestation of a tumor that is not part of lynch syndrome. [electronic resource] by
- Petersson, Fredrik
- Síma, Radek
- Sperga, Maris
- Kazakov, Dmitry V
- Michal, Michal
- Hora, Milan
- Ferda, Jiří
- Sulc, Miroslav
- Mičulka, Petr
- Haferník, Jiří
- Rychnovský, Jiří
- Hes, Ondřej
Producer: 20120229
In:
Applied immunohistochemistry & molecular morphology : AIMM vol. 19
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3937.
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Analysis of the oxidative damage repair genes NUDT1, OGG1, and MUTYH in patients from mismatch repair proficient HNPCC families (MSS-HNPCC). [electronic resource] by
- Garre, Pilar
- Briceño, Verónica
- Xicola, Rosa M
- Doyle, Brian J
- de la Hoya, Miguel
- Sanz, Julián
- Llovet, Patricia
- Pescador, Paula
- Puente, Javier
- Díaz-Rubio, Eduardo
- Llor, Xavier
- Caldés, Trinidad
Producer: 20110721
In:
Clinical cancer research : an official journal of the American Association for Cancer Research vol. 17
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3938.
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Risk Factors Associated with Colorectal Cancer in a Subset of Patients with Mutations in MLH1 and MSH2 in Taiwan Fulfilling the Amsterdam II Criteria for Lynch Syndrome. [electronic resource] by
- Kamiza, Abram Bunya
- Hsieh, Ling-Ling
- Tang, Reiping
- Chien, Huei-Tzu
- Lai, Chih-Hsiung
- Chiu, Li-Ling
- Lo, Tsai-Ping
- Hung, Kuan-Yi
- Wang, Chun-Yi
- You, Jeng-Fu
- Hsiung, Chao A
- Yeh, Chih-Ching
Producer: 20160425
In:
PloS one vol. 10
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3939.
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Functional analysis of MSH2 unclassified variants found in suspected Lynch syndrome patients reveals pathogenicity due to attenuated mismatch repair. [electronic resource] by
- Wielders, Eva A L
- Hettinger, Jan
- Dekker, Rob
- Kets, C Marleen
- Ligtenberg, Marjolijn J
- Mensenkamp, Arjen R
- van den Ouweland, Ans M W
- Prins, Judith
- Wagner, Anja
- Dinjens, Winand N M
- Dubbink, Hendrikus Jan
- van Hest, Liselotte P
- Menko, Fred
- Hogervorst, Frans
- Verhoef, Senno
- te Riele, Hein
Producer: 20141112
In:
Journal of medical genetics vol. 51
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3940.
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Frequent PIK3CA Mutations in Colorectal and Endometrial Tumors With 2 or More Somatic Mutations in Mismatch Repair Genes. [electronic resource] by
- Cohen, Stacey A
- Turner, Emily H
- Beightol, Mallory B
- Jacobson, Angela
- Gooley, Ted A
- Salipante, Stephen J
- Haraldsdottir, Sigurdis
- Smith, Christina
- Scroggins, Sheena
- Tait, Jonathan F
- Grady, William M
- Lin, Edward H
- Cohn, David E
- Goodfellow, Paul J
- Arnold, Mark W
- de la Chapelle, Albert
- Pearlman, Rachel
- Hampel, Heather
- Pritchard, Colin C
Producer: 20170529
In:
Gastroenterology vol. 151
Availability: No items available.
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