Deep Blue: Browsing Human Genetics, Department of by Title

Metabolomic profiles delineate potential role for sarcosine in prostate cancer progression

Sreekumar, Arun; Poisson, Laila M.; Rajendiran, Thekkelnaycke M.; Khan, Amjad P.; Cao, Qi; Yu, Jindan; Laxman, Bharathi; Mehra, Rohit; Lonigro, Robert J.; Li, Yong; Nyati, Mukesh K.; Ahsan, Aarif; Kalyana-Sundaram, Shanker; Han, Bo; Cao, Xuhong; Byun, Jaeman; Omenn, Gilbert S.; Ghosh, Debashis; Pennathur, Subramaniam; Alexander, Danny C.; Berger, Alvin; Shuster, Jeffrey R.; Wei, John T.; Varambally, Sooryanarayana; Beecher, Christopher A.; Chinnaiyan, Arul M. (Nature Publishing Group, 2008-02-11)

(851.6KB)

Microcephaly, jejunal atresia, aberrant right bronchus, ocular anomalies, and XY sex reversal

Keegan, Catherine E.; Vilain, Eric; Mohammed, Mansoor; Lehoczky, Jessica A.; Dobyns, William B.; Archer, Steven M.; Innis, Jeffrey W. (Wiley Subscription Services, Inc., A Wiley Company, 2004-03-15)

(147.5KB)

Mining Genetic Epidemiology Data with Bayesian Networks Application to APOE Gene Variation and Plasma Lipid Levels

Rodin, Andrei; Mosley, Thomas H.; Clark, Andrew G.; Sing, Charles F.; Boerwinkle, Eric (Mary Ann Liebert, Inc., publishers, 2005-02-01)

(294.2KB)

mnd2: A New Mouse Model of Inherited Motor Neuron Disease

Jones, Julie M.; Albin, Roger L.; Feldman, Eva L.; Simin, Karl; Schuster, Timothy G.; Dunnick, Wesley A.; Collins, John T.; Chrisp, Clarence E.; Taylor, Benjamin A.; Meisler, Miriam H. (Elsevier, 1993-06)

(928KB)

Modification of cell membrane in variants of chinese hamster cells resistant to abrin

Li, I-Chian; Blake, Diane A.; Goldstein, Irwin J.; Chu, Ernest H. Y. (Elsevier, 1980-10)

(740.8KB)

Modifications to the Patient Rule-Induction Method that utilize non-additive combinations of genetic and environmental effects to define partitions that predict ischemic heart disease

Dyson, Greg; Frikke-Schmidt, Ruth; Nordestgaard, Børge G.; Tybjæ;rg-Hansen, Anne; Sing, Charles F. (Wiley Subscription Services, Inc., A Wiley Company, 2009-05)

(144.2KB)

Molecular and cellular biology of von Willebrand factor

Lyons, Susan E.; Ginsburg, David W. (Elsevier, 1994)

(963.5KB)

Molecular and cytologic studies of Ehlers-Danlos syndrome type VIII

Biesecker, Leslie G.; Glover, Thomas W.; Bonadio, Jeffrey F. (Wiley Subscription Services, Inc., A Wiley Company, 1991-12-01)

(558.2KB)

Molecular and functional heterogeneity in dorsal and ventral oligodendrocyte progenitor cells of the mouse forebrain in response to DNA damage.

Boda, E; Lorenzati, M; Parolisi, R; Harding, B; Pallavicini, G; Bonfanti, L; Moccia, A; Bielas, S; Di Cunto, F; Buffo, A (Springer Nature, 2022-01-28)

(10.3MB)

Molecular basis of pituitary dysfunction in mouse and human

Cushman, Lisa J.; Camper, Sally A. (Springer-Verlag; Springer-Verlag New York Inc., 2001-07)

(119KB)

Molecular characterization of FRAXB and comparative common fragile site instability in cancer cells

Arlt, Martin F.; Miller, Diane E.; Beer, David G.; Glover, Thomas W. (John Wiley & Sons, Inc., 2002-01)

(146.6KB)

Molecular characterization of HOXA13 polyalanine expansion proteins in hand–foot–genital syndrome How to cite this article: Utsch B, McCabe CD, Galbraith K, Gonzalez R, Born M, DÖtsch J, Ludwig M, Reutter H, Innis JW. 2007. Molecular characterization of HOXA13 polyalanine expansion proteins in hand–foot–genital Syndrome. Am J Med Genet Part A 143A:3161–3168. Boris Utsch and Colleen D. McCabe contributed equally to this work.

Utsch, Boris; McCabe, Colleen D.; Galbraith, Kenneth; Gonzalez, Ricardo; Born, Mark; Dötsch, Jörg; Ludwig, Michael; Reutter, Heiko; Innis, Jeffrey W. (Wiley Subscription Services, Inc., A Wiley Company, 2007-12-15)

(272.1KB)

Molecular genetics (Methods in hematology vol. 20) : edited by Edward J. Benz, Jr, Churchill Livingstone, 1990, [UK pound]35.00 (v + 208 pages) ISBN 0 443 03852 X

Ginsburg, David W. (Elsevier, 1990)

(161.9KB)

Mouse Chromosome 10

Bureau, Jean-Francois; Burmeister, Margit L.; Bryda, Elizabeth C.; Noben-Trauth, Konrad (Springer-Verlag; Springer-Verlag New York Inc., 1999-10)

(21KB)

Mouse chromosome 10

Frankel, Wayne N.; Burmeister, Margit L.; Taylor, Benjamin A.; Bryda, Elizabeth C. (Springer-Verlag, 1993-01)

(770.9KB)

Mouse chromosome 11

Buchberg, Arthur M.; Camper, Sally A. (Springer-Verlag, 1993-01)

(1MB)

Mouse Chromosome 11

Camper, Sally A.; Buchberg, Arthur M.; Buckwalter, Marion S. (Springer-Verlag, 1992-01)

(1.7MB)

Mouse chromosome 3

Todd, John A.; Seldin, Michael F.; Prins, Jan-Bas; Rodrigues, Nanda R.; Meisler, Miriam H. (Springer-Verlag, 1993-01)

(799KB)

Mouse Chromosome 3

Wakeland, Edward K.; Seldin, Michael F.; Rodrigues, Nanda R.; Todd, John A.; Meisler, Miriam H. (Springer-Verlag, 1992-01)

(949.3KB)

Mouse chromosome 3

Meisler, Miriam H. (Springer-Verlag; Springer-Verlag New York Inc., 1991-03)

(787.3KB)

Multicolor FISH Mapping of YAC Clones in 3p14 and Identification of a YAC Spanning both FRA3B and the t(3;8) Associated with Hereditary Renal Cell Carcinoma

Wilke, Charles M.; Guo, Sun-Wei; Hall, Bryan K.; Boldog, Ferenc; Gemmill, Robert M.; Chandrasekharappa, Settara C.; Barcroft, Christine L.; Drabkin, Harry A.; Glover, Thomas W. (Elsevier, 1994-07-15)

(551.6KB)

Multicolor FISH Mapping with Alu-PCR-Amplified YAC Clone DNA Determines the Order of Markers in the BRCA1 Region on Chromosome 17q12-q21

Flejter, Wendy L.; Barcroft, Christine L.; Guo, Sun-Wei; Lynch, Eric D.; Boehnke, Michael; Chandrasekharappa, Settara C.; Hayes, Steve T.; Collins, Francis S.; Weber, Barbara L.; Glover, Thomas W. (Elsevier, 1993-09)

(569KB)

Multiple forms of genetic instability within a 2-Mb chromosomal segment of 3q26.3–q27 are associated with development of esophageal adenocarcinoma

Lin, Lin; Wang, Zhuwen; Prescott, Michael S.; van Dekken, Herman; Thomas, Dafydd G.; Giordano, Thomas J.; Chang, Andrew C.; Orringer, Mark B.; Gruber, Stephen B.; Moran, John V.; Glover, Thomas W.; Beer, David G. (Wiley Subscription Services, Inc., A Wiley Company, 2006-04)

(811KB)

Mutants of chinese hamster cells deficient in thymidylate synthetase

Li, I-Chian; Chu, Ernest H. Y. (Wiley Subscription Services, Inc., A Wiley Company, 1984-08)

(740.1KB)

Mutation analysis in nephronophthisis using a combined approach of homozygosity mapping, CEL I endonuclease cleavage, and direct sequencing Communicated by Peter Byers

Otto, Edgar A.; Helou, Juliana; Allen, Susan J.; O'Toole, John F.; Wise, Eric L.; Ashraf, Shazia; Attanasio, Massimo; Zhou, Weibin; Wolf, Matthias T. F.; Hildebrandt, Friedhelm (Wiley Subscription Services, Inc., A Wiley Company, 2008-03)

(330.4KB)