A Gene Transcribed from the Bidirectional ATM Promoter Coding for a Serine Rich Protein: Amino Acid Sequence, Structure and Expression Studies (English)
- New search for: Byrd, Philip J.
- New search for: Cooper, Paul R.
- New search for: Stankovic, Tatjana
- New search for: Kullar, Harjit S.
- New search for: Watts, Giles D. J.
- New search for: Robinson, Paula J.
- New search for: Malcolm, A.
- New search for: Taylor, R.
- New search for: Byrd, Philip J.
- New search for: Cooper, Paul R.
- New search for: Stankovic, Tatjana
- New search for: Kullar, Harjit S.
- New search for: Watts, Giles D. J.
- New search for: Robinson, Paula J.
- New search for: Malcolm, A.
- New search for: Taylor, R.
In:
Human molecular genetics
;
5
, 11
;
1785-
;
1996
- Article (Journal) / Electronic Resource
-
Title:A Gene Transcribed from the Bidirectional ATM Promoter Coding for a Serine Rich Protein: Amino Acid Sequence, Structure and Expression Studies
-
Contributors:Byrd, Philip J. ( author ) / Cooper, Paul R. ( author ) / Stankovic, Tatjana ( author ) / Kullar, Harjit S. ( author ) / Watts, Giles D. J. ( author ) / Robinson, Paula J. ( author ) / Malcolm, A. ( author ) / Taylor, R. ( author )
-
Published in:Human molecular genetics ; 5, 11 ; 1785-
-
Publisher:
- New search for: Oxford University Press
-
Publication date:1996-11-01
-
ISSN:
-
DOI:
-
Type of media:Article (Journal)
-
Type of material:Electronic Resource
-
Language:English
-
Source:
Table of contents – Volume 5, Issue 11
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 1695
-
The Drosophila Developmental Gene Fat Facets Has a Human Homologue in Xp11.4 Which Escapes X-inactivation and Has Related Sequences on Yq11.2Jones, Michael H. / Furlong, Robert A. / Burkin, Heather / Jennifer Chalmers, I. / Brown, Graeme M. / Khwaja, Omar / Affara, Nabeel A. et al. | 1996
- 1703
-
Immunology of Gene Therapy with Adenoviral Vectors in Mouse Skeletal MuscleYang, Yiping / Ehlen Haecker, Sarah / Su, Qin / Wilson, James M. et al. | 1996
- 1713
-
A 94 kb Genomic Sequence 3' to the Murine Xist Gene Reveals an AT Rich Region Containing a New Testis Specific Gene TsxSimmler, Marie-Christine / Cunningham, David B. / Clerc, Philippe / Vermat, Thierry / Caudron, Bernard / Cruaud, Corinne / Pawlak, André / Szpirer, Claude / Weissenbach, Jean / Claverie, Jean-Michel et al. | 1996
- 1727
-
An 11 Base Pair Duplication in Exon 6 of the SMN Gene Produces a Type I Spinal Muscular Atrophy (SMA) Phenotype: Further Evidence For SMN as the Primary SMA-Determining GeneParsons, D. Williams / McAndrew, Patricia E. / Monani, Umrao R. / Mendell, Jerry R. / Burghes, Arthur H. M. / Prior, Thomas W. et al. | 1996
- 1733
-
A splice-junction mutation in the region of COL5A1 that codes for the carboxyl propeptide of pro1(V) chains results in the gravis form of the Ehlers-Danlos syndrome (type I)Wenstrup, R. J. / Langland, G. T. / Willing, M. C. / D'Souza, V. N. / Cole, W. G. et al. | 1996
- 1733
-
A Splice-Junction Mutation in the Region of COL5A1 that Codes for the Carboxyl Propeptide of Pro{alpha}1(V) Chains Results in the Gravis Form of the Ehlers-Danlos Syndrome (Type I)Wenstrup, Richard J. / Langland, Gregory T. / Willing, Marcia C. / D'Souza, Vinita N. / Cole, William G. et al. | 1996
- 1737
-
A Repeated Element in the Regulatory Region of the MNK Gene and Its Deletion in A Patient With Occipital Horn SyndromeLevinson, Barbara / Conant, Rebecca / Schnur, Rhonda / Das, Soma / Packman, Seymour / Gitschier, Jane et al. | 1996
- 1743
-
A Novel Human Homologue of Yeast Nucleosome Assembly Protein, 65 kb Centromeric to the p57KIP2 Gene, is Biallelically Expressed in Fetal and Adult TissuesHu, Ren-Ju / Lee, Maxwell P. / Johnson, Laura A. / Feinberg, Andrew P. et al. | 1996
- 1749
-
Alternate Promoters and Alternate Splicing of Human Tenascin-X, a Gene with 5' and 3' Ends Buried in Other GenesSpeek, Mart / Barry, Floyd / Miller, Walter L. et al. | 1996
- 1759
-
Network Analysis of Human Y Microsatellite HaplotypesCooper, Gillian / Amos, William / Hoffman, Dorota / Rubinsztein, David C. et al. | 1996
- 1767
-
Recurrent Duplication and Deletion Polymorphisms on the Long Arm of the Y Chromosome in Normal MalesJobling, Mark A. / Samara, Vassiliki / Pandya, Arpita / Fretwell, Neale / Bernasconi, Barbara / Mitchell, R. John / Gerelsaikhan, Tudevdagva / Dashnyam, Bumbein / Sajantila, Antti / Salo, Pia J. et al. | 1996
- 1777
-
Selection Against Mutant Alleles in Blood Leukocytes is a Consistent Feature in Incontinentia Pigmenti Type 2Parrish, Julia E. / Scheuerle, Angela E. / Lewis, Richard A. / Levy, Moise L. / Nelson, David L. et al. | 1996
- 1785
-
A Gene Transcribed from the Bidirectional ATM Promoter Coding for a Serine Rich Protein: Amino Acid Sequence, Structure and Expression StudiesByrd, Philip J. / Cooper, Paul R. / Stankovic, Tatjana / Kullar, Harjit S. / Watts, Giles D. J. / Robinson, Paula J. / Malcolm, A. / Taylor, R. et al. | 1996
- 1793
-
Oligonucleotide Probes for Alpha Satellite DNA Variants Can Distinguish Homologous Chromosomes by FISHO'Keefe, Christine L. / Warburton, Peter E. / Matera, A. Gregory et al. | 1996
- 1801
-
Testis-Specific Protein, Y-Encoded (TSPY) Expression in Testicular TissuesSchnieders, Frank / Dörk, Thilo / Arnemann, Joachim / Vogel, Tanja / Werner, Martin / Schmidtke, Jörg et al. | 1996
- 1809
-
Mutation of the Pancreatic Islet Inward Rectifier Kir6.2 Also Leads to Familial Persistent Hyperinsulinemic Hypoglycemia of InfancyThomas, Pamela / Ye, Yuyang / Lightner, Elmer et al. | 1996
- 1809
-
Mutation of the pancreatic islet inward rectifier Kir6.2 also lends to familial persistent hyperinsulinemic hypoglycemia of infancyThomas, P. / Ye, Y. / Lightner, E. et al. | 1996
- 1813
-
Mutations in the Sulfonylurea Receptor Gene Are Associated with Familial Hyperinsulinism in Ashkenazi JewsNestorowicz, Ann / Wilson, Beth Anne / Schoor, Kathleen P. / Inoue, Hiroshi / Glaser, Benjamin / Landau, Heddy / Stanley, Charles A. / Thornton, Paul S. / Clement, John P. / Bryan, Joseph et al. | 1996
- 1823
-
Mutation Rate Heterogeneity and the Generation of Allele Diversity at the Human Minisatellite MS205 (D16S309)May, Celia A. / Jeffreys, Alec J. / Armour, John A. L. et al. | 1996
- 1835
-
A Novel Heteroplasmic tRNAleu(CUN) mtDNA Point Mutation in a Sporadic Patient With Mitochondrial Encephalomyopathy Segregates Rapidly in Skeletal Muscle and Suggests an Approach to TherapyFu, Katherine / Hartlen, Rebecca / Johns, Timothy / Genge, Angela / Karpati, George / Shoubridge, Eric A. et al. | 1996
- 1841
-
Mutations That Disrupt the Carboxyl-Terminus of {gamma}-Sarcoglycan Cause Muscular DystrophyMcNally, Elizabeth M. / Duggan, David / Rafael Gorospe, J. / Bönnemann, Carsten G. / Fanin, Marina / Pegoraro, Elena / Lidov, Hart G. W. / Noguchi, Satoru / Ozawa, Eijiro / Finkel, Richard S. et al. | 1996