Deep Blue: Browsing by Title

Mutation location on the RAS oncogene affects pathologic features and survival after resection of colorectal liver metastases

Frankel, Timothy L.; Vakiani, Efsevia; Nathan, Hari; DeMatteo, Ronald P.; Kingham, T. Peter; Allen, Peter J.; Jarnagin, William R.; Kemeny, Nancy E.; Solit, David B.; D’Angelica, Michael I. (Wiley Periodicals, Inc., 2017-02-15)

(1.2MB)

(376.5KB)

Mutation matrices and physical-chemical properties: Correlations and implications

Koshi, Jeffrey M.; Goldstein, Richard A. (Wiley Subscription Services, Inc., A Wiley Company, 1997-03)

(86.4KB)

Mutation of FIG4 causes neurodegeneration in the pale tremor mouse and patients with CMT4J

Chow, Clement Y.; Zhang, Yanling; Dowling, James J.; Jin, Natsuko; Adamska, Maja; Shiga, Kensuke; Szigeti, Kinga; Shy, Michael E.; Li, Jun; Zhang, Xuebao; Lupski, James R.; Weisman, Lois S.; Meisler, Miriam H. (Nature Publishing Group, 2007-07-05)

(892.8KB)

The mutation Ser2117Leu, in the second hydrophobic spike of the factor V C2 domain, increases phospholipid affinity and specific activity

Gilbert, G. E.; Kaufman, R. J.; Price, P.; Miao, H.; Pipe, S. (Wiley Periodicals, Inc., 2003-07)

(28.9KB)

Mutation spectrum in the large GTPase dynamin 2, and genotype–phenotype correlation in autosomal dominant centronuclear myopathy

Sikkema‐raddatz, Birgit; Sijmons, Rolf H. (Wiley Subscription Services, Inc., A Wiley Company, 2012-06)

(615.2KB)

(195.3KB)

MUTATION SYSTEMS IN CULTURED MAMMALIAN CELLS *

Chu, Ernest H. Y. (Blackwell Publishing Ltd, 1983-06)

(623.8KB)

Mutation To 6-thioguanine Resistance In Human Lymphocyte Lines.

Powell, Sandra Anita Streeter (1975)

(2.9MB)

Mutation update for the SATB2 gene

Zarate, Yuri A.; Bosanko, Katherine A.; Caffrey, Aisling R.; Bernstein, Jonathan A.; Martin, Donna M.; Williams, Marc S.; Berry‐kravis, Elizabeth M.; Mark, Paul R.; Manning, Melanie A.; Bhambhani, Vikas; Vargas, Marcelo; Seeley, Andrea H.; Estrada‐veras, Juvianee I.; Dooren, Marieke F.; Schwab, Maria; Vanderver, Adeline; Melis, Daniela; Alsadah, Adnan; Sadler, Laurie; Esch, Hilde; Callewaert, Bert; Oostra, Ann; Maclean, Jane; Dentici, Maria Lisa; Orlando, Valeria; Lipson, Mark; Sparagana, Steven P.; Maarup, Timothy J.; Alsters, Suzanne IM; Brautbar, Ariel; Kovitch, Eliana; Naidu, Sakkubai; Lees, Melissa; Smith, Douglas M.; Turner, Lesley; Raggio, Víctor; Spangenberg, Lucía; Garcia‐miñaúr, Sixto; Roeder, Elizabeth R.; Littlejohn, Rebecca O.; Grange, Dorothy; Pfotenhauer, Jean; Jones, Marilyn C.; Balasubramanian, Meena; Martinez‐monseny, Antonio; Blok, Lot Snijders; Gavrilova, Ralitza; Fish, Jennifer L. (GeneReviews(R)Wiley Periodicals, Inc., 2019-08)

(474.7KB)

(3.3MB)

(514KB)

Mutation Watch

Meisler, Miriam H. (Springer-Verlag; Springer-Verlag New York Inc., 1997-05)

(27.8KB)

Mutation watch: Mouse brachyury ( T ), the T-box gene family, and human disease

Meisler, Miriam H. (Springer-Verlag; Springer-Verlag New York Inc., 1997-11)

(20.5KB)

Mutation watch:PEX PLUS? Gene(s) for X-linked hypophosphatemia and deafness

Meisler, Miriam H. (Springer-Verlag; Springer-Verlag New York Inc., 1997-08)

(28.3KB)

Mutation-absorption model of the enzyme

Conrad, Michael (Elsevier, 1979)

(1.3MB)

Mutational analyses of yeast nuclear RNase P.

Pagan-Ramos, Eileen (1996)

(7.6MB)

Mutational analysis of candidate genes in 24 amelogenesis imperfecta families

Kim, Jung-Wook; Simmer, James P.; Lin, Brent P.-L.; Seymen, Figen; Bartlett, John D.; Hu, Jan C-C. (Blackwell Publishing Ltd, 2006-05)

(535.9KB)

Mutational analysis of DsbA and DsbB, two disulfide catalysts, to identify critical residues involved in their functions.

Tan, Jacqueline Teng Teng (2004)

(7.4MB)

Mutational analysis of the NPHP4 gene in 250 patients with nephronophthisis Communicated by JÜrgen Horst Online Citation: Human Mutation , Mutation in Brief #797 (2005) Online http://www3.interscience.wiley.com/homepages/38515/pdf/797.pdf

Hoefele, Julia; Sudbrak, Ralf; Reinhardt, Richard; Lehrack, Silvia; Hennig, Steffen; Imm, Anita; Muerb, Ulla; Utsch, Boris; Attanasio, Massimo; O'Toole, John F.; Otto, Edgar A.; Hildebrandt, Friedhelm (Wiley Subscription Services, Inc., A Wiley Company, 2005-04)

(131.6KB)

Mutational analysis of the insulin-dependent enhancer from the mouse amylase gene Amy-2.2.

Johnson, Thomas Martin (1991)

(4.1MB)

Mutational analysis of the β -subunit of yeast geranylgeranyl transferase I

Pringle, John R.; Ohya, Yoshikazu; Caplin, Brian E.; Qadota, Hiroshi; Tibbetts, Michael F.; Marshall, Mark S.; Anraku, Yasuhiro (Springer-Verlag, 1996-08)

(1.6MB)

Mutational analysis of the β-subunit of yeast geranylgeranyl transferase I

Qadota, Hiroshi; Pringle, John R.; Caplin, Brian E.; Ohya, Yoshikazu; Marshall, Mark S.; Anraku, Yasuhiro; Tibbetts, Michael F. (Springer-Verlag; Springer-Verlag Berlin Heidelberg, 1996-08)

(713.4KB)

Mutational hot spot in the DSPP gene causing dentinogenesis imperfecta type II

Kim, Jung-Wook; Hu, Jan C-C.; Jang, Ki-Taeg; Kim, Young-Jae; Lee, Jae-Il; Moon, Sung-Kwon; Hahn, Se-Hyun; Lee, Sang-Hoon; Kim, Chong-Chul; Simmer, James P. (Springer-Verlag, 2005-02)

(334.5KB)

Mutational landscape of candidate genes in familial prostate cancer

Johnson, Anna M.; Zuhlke, Kimberly A.; Plotts, Chris; McDonnell, Shannon K.; Middha, Sumit; Riska, Shaun M.; Schaid, Daniel J.; Thibodeau, Stephen N.; Douglas, Julie A.; Cooney, Kathleen A. (Wiley Periodicals, Inc., 2014-10)

(146.2KB)

(351.8KB)

Mutational profiles of persistent/recurrent laryngeal squamous cell carcinoma

Smith, Joshua D.; Birkeland, Andrew C.; Rosko, Andrew J.; Hoesli, Rebecca C.; Foltin, Susan K.; Swiecicki, Paul; Mierzwa, Michelle; Chinn, Steven B.; Shuman, Andrew G.; Malloy, Kelly M.; Casper, Keith A.; McLean, Scott A.; Wolf, Gregory T.; Bradford, Carol R.; Prince, Mark E.; Brenner, John Chad; Spector, Matthew E. (Wiley Periodicals, Inc., 2019-02)

(684.4KB)

(276.7KB)

Mutational spectrum of FAM83H : the C-terminal portion is required for tooth enamel calcification Communicated by Mark H. Paalman

Lee, Sook-Kyung; Hu, Jan C-C.; Bartlett, John D.; Lee, Kyung-Eun; Lin, Brent P-J.; Simmer, James P.; Kim, Jung-Wook (Wiley Subscription Services, Inc., A Wiley Company, 2008-08)

(148.3KB)

Mutations in KCND3 cause spinocerebellar ataxia type 22

Lee, Yi‐chung; Durr, Alexandra; Majczenko, Karen; Huang, Yen‐hua; Liu, Yu‐chao; Lien, Cheng‐chang; Tsai, Pei‐chien; Ichikawa, Yaeko; Goto, Jun; Monin, Marie‐lorraine; Li, Jun Z.; Chung, Ming‐yi; Mundwiller, Emeline; Shakkottai, Vikram; Liu, Tze‐tze; Tesson, Christelle; Lu, Yi‐chun; Brice, Alexis; Tsuji, Shoji; Burmeister, Margit; Stevanin, Giovanni; Soong, Bing‐wen (Wiley Subscription Services, Inc., A Wiley Company, 2012-12)

(823.8KB)

Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura

Levy, G. G.; Nichols, William C.; Lian, E. C.; Foroud, Tatiana; McClintick, J. N.; McGee, B. M.; Yang, Angela Y.; Siemieniak, David R.; Stark, K. R.; Gruppo, R.; Sarode, R.; Shurin, S. B.; Chandrasekaran, V.; Stabler, S. P.; Sabio, H.; Bouhassira, E. E.; Upshaw, J. D.; Ginsburg, David W.; Tsai, H. M. (Macmillan Publishers Ltd., 2001-10-04)

(304.3KB)