Identification of conserved potentially regulatory sequences of the SRY gene from 10 different … - Full text - MIT Libraries
E Margarit, A Guillen, C Rebordosa, J Vidal- … - Biochem Biophys Res Commun, 1998 - ingentaconnect.com
... Ten highly conserved potential regulatory elements have been identified in all 10
species (AP1, Barbie, GATA, Gfi1, cMyb, vMyb, NF1, Oct1, Sp1, and SRY). ...
Cited by 18 - Web Search - ingentaconnect.com - ncbi.nlm.nih.gov

Brief Clinical Report A Man Who Inherited His SRY Gene and Leri-Weill Dyschondrosteosis From His … - Full text - MIT Libraries
JL Ross, AR Zinn - American Journal of Medical Genetics, 2001 - doi.wiley.com
... His father had NF1. His ... DYZ1‡). The dic(X;Y) chromosome was also positive
for Y markers PABY, SRY, and DYZ5, but negative for SHOX. ...
Web Search - doi.wiley.com

Gene expression profiling of cultured human NF1 heterozygous (NF1) melanocytes reveals … - Full text - MIT Libraries
J Boucneau, S De Schepper, M Vuylsteke, P Van … - Pigment Cell Research, 2005 - blackwell-synergy.com
... HMG-box domain containing transcription factors belong to the SOX (SRY-related HMG ...
our study, both SOX4 and SOX10 are downregulated in NF1 +/ (CALM) melanocytes ...
Web Search - ingentaconnect.com

REGULATION TRANSCRIPTIONNELLE DU GENE SRY HUMAIN ET PORCIN PAR LE FACTEUR DE TRANSCRIPTION GATA-4.
F DE MEDECINE - theses.ulaval.ca
... Gfi1, cMyb, vMyb, NF1, Oct1, Sp1 et SRY) sans toutefois de conservation
au niveau de leur position dans le promoteur (57;58). De ...
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In simple synthetic promoters YY 1-induced DNA bending is important in transcription activation and … - Full text - MIT Libraries
J Kim, DJ Shapiro - Nucleic Acids Research, 1996 - nar.oupjournals.org
... Deletion of 4 bp between the NF1 and YY1 sites, which changes the phase of the DNA ...
transcription regulators are LEF1 ( 27 , 28 ), HMG I/Y ( 29 ), SRY ( 30 , 31 ...
Cited by 23 - Web Search - nar.oupjournals.org - pubmedcentral.nih.gov - ncbi.nlm.nih.gov - all 5 versions »

A man who inherited hisSRY gene and Leri-Weill dyschondrosteosis from his mother and … - Full text - MIT Libraries
F Wei, S Cheng, N Badie, F Elder, C Scott, L … - American Journal of Medical Genetics, 2001 - ncbi.nlm.nih.gov
Click here to read A man who inherited his SRY gene and Leri-Weill ... We report on a
man with neurofibromatosis type 1 (NF1) and Leri-Weill dyschondrosteosis (LWD ...
Cited by 2 - Web Search

Mouse GLUT8: genomic organization and regulation of expression in 3T3-L1 adipocytes by glucose - Full text - MIT Libraries
A Scheepers, H Doege, HG Joost, A Schurmann - Biochem. Biophys. Res. Commun, 2001 - ingentaconnect.com
... This region comprises a CAAT box and consensus binding sites for the transcription
factors SRY and NF1 that were highly conserved in the mouse and in the human ...
Cited by 8 - Web Search - ingentaconnect.com - ncbi.nlm.nih.gov

Computational analysis of composite regulatory elements - Full text - MIT Libraries
P Qiu, W Ding, Y Jiang, JR Greene, L Wang - Mammalian Genome, 2002 - springerlink.com
... SRY 81.9 CREB USF 35.0 TATA YY1 21.6 CREBP1 CREBP1 265.6 RORA2 TCF11 80.9 GR HNF4
34.9 AHRARNT ATF 21.6 BRN2 TATA 257.1 HNF4 RORA1 80.4 CREB SRF 34.4 CHOP NF1 ...
Cited by 10 - Web Search - ncbi.nlm.nih.gov

The joys of reverse biology.
P Child, F Chromosomes, M Cloning, TS Genes, H … - Nat Genet, 1993 - ncbi.nlm.nih.gov
... Repetitive Sequences, Nucleic Acid; Sequence Homology*. Gene Symbols: BRCA1;
FMR-1; NF1; PAX6; PMP-22; Pit-1; SRY; Skn-1; WT1. PMID: 8099840 [PubMed - indexed ...
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James M. Boughton
WH Branson, A Muttardy - dsl.nber.org
... Page 16. RFLAFIVF EFFECTS OF N1S)NF1 SRY FNIANSTS)N — — ISItAIIVE FIIF( IS OF
1-ISCAL 31511 RLIASCE / / / / / P. RELA1IVE EFFECTS OF SUPPLY DISiL RISASCE ...
Web Search

Cloning and characterization of the 5-flanking region of the rat glutamate-cysteine ligase catalytic … - Full text - MIT Libraries
Y Heping, W Jiaohong, ZZ HUANG, OU Xiaopeng, C … - Biochem. J, 2001 - biochemj.org
... or light subunit; HSF, heat-shock transcription factor; MZF1, myeloid zinc finger
1; NF1, nuclear factor 1; NF-κB, nuclear factor κB; SRY, sex-determining ...
Cited by 9 - View as HTML - Web Search - biochemj.org - ncbi.nlm.nih.gov - ncbi.nlm.nih.gov

Systematic multiplex polymerase chain reaction and reverse transcription-polymerase chain reaction … - Full text - MIT Libraries
SYU Clinic, J Sendai - Electrophoresis, 2004 - doi.wiley.com
... APC, BRCA1, BRCA2, CDKN2A, CDKN2B, NF1, PTEN, TP53, TP73, VHL, WT1 tumor suppressor
genes. ATRX and NSBP1 X chromosome-linked genes and RBMY2B, SRY, and TSPY Y ...
Web Search - ncbi.nlm.nih.gov

Plenary Lectures
H van den Berghe, GP Holmquist - Cytogenet Cell Genet, 1999 - content.karger.com
... Trent, JM, and Marchuk, DA Identification and mapping of type 1 neurofibromatosis
(NF1) homologous loci. ... (ii) The primary sex determining locus SRY, must avoid ...
Web Search

Human testis expresses a specific poly (A)-binding protein - Full text - MIT Libraries
C Feral, G Guellaen, A Pawlak - Nucleic Acids Research, 2001 - nar.oupjournals.org
... 0.87). Other motifs meeting the above criteria are not shown: BRN2, CETS1P54,
E47, FREAC7, IK2, LMO2COM, SRY, NF1, ROX and XFD2. The ...
Cited by 12 - Web Search - pubmedcentral.nih.gov - ingentaconnect.com - ncbi.nlm.nih.gov - all 7 versions »

The evolution of isochores - Full text - MIT Libraries
A Eyre-Walker, LD Hurst - Nat. Rev. Genet, 2001 - nature.com
... differ- ent times at which these regions replicate (with the (G+C)-rich region
replicating earli- er) 6 ; the boundary at the neurofibromatosis (NF1) region is ...
Cited by 71 - Web Search - entomology.wisc.edu - lifesci.sussex.ac.uk - biols.susx.ac.uk - all 11 versions »

Status of the Human Malformation Map: 2002
JC CAREY, DH VISKOCHIL - American Journal of Medical Genetics (Semin. Med. Genet.), 2002 - doi.wiley.com
... Sonic hedgehog), ligands (FGFR1-3), signal transduction pathway genes (NF1),
extracellular matrix proteins ... dysplasia 114290 114290 17q24.3-q25.1 SOX9 SRY-box ...
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Tissue culture methods to study neurological disorders: Establishment of immortalized Schwann cells … - Full text - MIT Libraries
K Watabe, T Sakamoto, Y Kawazoe, M Michikawa, K … - Neuropathology, 2003 - ingentaconnect.com
... nih /+), myelin P0 protein-deficient mice (P0–/–, P0+/–) with their wild-type
littermates (P0+/+), and neurofibromatosis type 1 gene (NF1)-deficient mice ...
Cited by 2 - Web Search - ncbi.nlm.nih.gov

DAX-1, an unusual orphan receptor at the crossroads of steroidogenic function and sexual … - Full text - MIT Libraries
E Lalli, P Sassone-Corsi - Mol Endocrinol, 2003 - mend.endojournals.org
... represents an « antitestis » gene, antagonizing Sry function and required for ... protein),
and ubiquitous transcription factors NF1 (nuclear factor 1) and Sp1 ...
Cited by 11 - Web Search - mend.endojournals.org - ncbi.nlm.nih.gov - ncbi.nlm.nih.gov

A novel computational approach for the prediction of networked transcription factors of Ah-receptor … - Full text - MIT Libraries
A Kel, S Reymann, V Matys, P Nettesheim, E … - Molecular Pharmacology, 2004 - molpharm.aspetjournals.org
Page 1. MOL Manuscript # 1677R 1 A novel computational approach for the prediction
of networked transcription factors of Ah-receptor regulated genes . ...
Cited by 3 - Web Search - molpharm.org - molpharm.aspetjournals.org - ncbi.nlm.nih.gov - all 5 versions »

Insertions, substitutions, and the origin of microsatellites - Full text - MIT Libraries
Y ZHU, JE STRASSMANN, DC QUELLER - Genetical Research, 2000 - journals.cambridge.org
... (1991) 10 hMSH2 GACtaTTTAC No Maliaka et al. (1996) 11 NF1 AGTTttACTG No Ainsworth
et al. (1993) ... (1997) 20 SRY TTgtagGTAGCT Yes (1) Foster et al. (1994) ...
Cited by 9 - Web Search - ruf.rice.edu - dx.doi.org - ncbi.nlm.nih.gov - all 5 versions »

Identical mutations and phenotypic variation - Full text - MIT Libraries
U Wolf - Human Genetics, 1997 - springerlink.com
... and III 4 families SOX9 17q24.3- Frameshift after SRY-related Campomelic
dysplasia Two unrelated Kwok et al. 1995 q25.1 codon 368 ...
Cited by 54 - Web Search - ncbi.nlm.nih.gov - ncbi.nlm.nih.gov

Transcriptional regulation of cardiac development: implications for congenital heart disease and … - Full text - MIT Libraries
JA Epstein, CA Buck - Pediatr Res, 2000 - pedresearch.org
... Transcriptional regulators such as NFATc, the Sry-related homeobox gene Sox4 ...
ras-GAP protein encoded by the Neurofibromatosis gene NF1 disrupt valvulogenesis ( ...
Cited by 19 - Web Search - pedresearch.org - ncbi.nlm.nih.gov

The river buffalo(Bubalus bubalis, 2 n= 50) cytogenetic map: assignment of 64 loci by fluorescence … - Full text - MIT Libraries
L Iannuzzi, GP Di Meo, A Perucatti, L Schibler, D … - Cytogenetic and Genome Research, 2003 - content.karger.com
... Sixty-four genomic BAC-clones mapping five type I (ADCYAP1, HRH1, IL3, RBP3B and
SRY) and 59 type II loci, previously FISH-mapped to goat (63 loci) and cattle ...
Cited by 1 - Web Search - dx.doi.org - karger.com - ncbi.nlm.nih.gov - all 5 versions »

LACK OF EVIDENCE OF PERMANENT ENGRAFTMENT AFTER IN UTERO FETAL STEM CELL TRANSPLANTATION IN …
OV Cervello, C Articles - Transplantation, 1996 - transplantjournal.com
... at the NF1 locus (Alu repeat) (15), and the Rb1 locus (16), and for the presence
of Y chromosome-specific sequences by amplification of the SRY (17) or the ...
Cited by 38 - Web Search - ncbi.nlm.nih.gov - Get it from MIT Libraries

Divergent outcomes of intrachromosomal recombination on the human Y chromosome: male infertility and … - Full text - MIT Libraries
P Blanco, M Shlumukova, CA Sargent, MA Jobling, N … - Journal of Medical Genetics, 2000 - jmedgenet.com
... of the YAP insertion 23 and the derived form of the SRY-1532 polymorphism ... Marynen
P, Legius E. Unequal meiotic crossover: a frequent cause of NF1 microdeletions ...
Cited by 49 - Cached - Web Search - jmg.bmjjournals.com - dx.doi.org - ncbi.nlm.nih.gov - all 6 versions »

Etablierung von in vitro Testsystemen zur Erfassung androgener/antiandrogener Wirkungen und …
S Guth - kluedo.ub.uni-kl.de
... [Danzo, 1998] Abb.1: Geschlechtsdifferenzierung bei Säugern [nach Spindler, 1997]
SRY = Sex determining region Y; ... XX Hoden; SRY Leydig-Zellen Sertoli-Zellen ...
View as HTML - Web Search - kluedo.ub.uni-kl.de - deposit.ddb.de

BMC Bioinformatics - Full text - MIT Libraries
SD Mooney, TE Klein - BMC Bioinformatics, 2002 - biomedcentral.com
... ATP7A 0.62 GALE 0.75 NAGA 1.01 SLC2A2 0.58 ATP7B 0.36 GALK1 1.18 NF1 1.05
SLC3A1 0.89 AVP ... 0.17 CACNA1S 0.91 GLA 0.63 OTC 0.71 SRY 0.46 ...
View as HTML - Web Search - bmc.ub.uni-potsdam.de - gdrs-intranet.ath.cx - smi-web.stanford.edu - all 6 versions »

Deciphering transcriptional regulation relevant to eating behavior
DM Graunke, G Argyropoulos - Current Genomics, 2003 - ingentaconnect.com
... IF2 √ NF1 √ Antp √ ... hAgRP (−1320/−1306) 5'-TTGCTTCATTTCATT-3' hNPY AP-1,C/EBPγ,
SRY hAgRP (−19,894/−19,880) 5'-ACACAAGAACAAACC-3' hNPY LEF-1 ...
Cited by 2 - Web Search

REVIEW ARTICLES Transcriptional Regulation of Cardiac Development: Implications for Congenital Heart …
JA EPSTEIN, CA BUCK - PEDIATRIC RESEARCH, 2000 - uphs.upenn.edu
... Transcriptional regulators such as NFATc, the Sry- related homeobox gene Sox4 ...
ras-GAP protein encoded by the Neurofibromatosis gene NF1 disrupt valvulogenesis ...
View as HTML - Web Search - Get it from MIT Libraries

Developmental Biology: Frontiers for Clinical Genetics Fishing for new genes in skin biology: impact … - Full text - MIT Libraries
M Tadin-Strapps, D Warburton, JC Salas-Alanis, LD … - Clinical Genetics, 2004 - blackwell-synergy.com
... foot malformation-1 (SHFM-1) and Sex-determining region-Y (SRY) where chromosomal ...
gene: identification of a large transcript disrupted in three NF1 patients. ...
Web Search - ncbi.nlm.nih.gov

Functional characterization and genomic organization of the human Na-sulfate cotransporter hNaS2 … - Full text - MIT Libraries
D Markovich, RR Regeer, K Kunzelmann, PA Dawson - Biochemical and Biophysical Research Communications, 2005 - uq.edu.au
... activator 2; Sox-5, SRY-related HMG box; HNF4, hepatic nuclear factor 4; SMAD4,
smad4 transcription factor involved in TGF-b signaling; NF1, nuclear factor 1 ...
Cited by 1 - View as HTML - Web Search - ncbi.nlm.nih.gov

Transcription Factors
S Veeraraghavan - www-bmb.med.uth.tmc.edu
... Sp1 (100 kD) from mammalian cells binds GC containing promoters CTF (CCAAT-binding
factor or NF1, 60 kD) mammalian cells ... [HMG I(Y)] HMG-box proteins SRY and ...
View as HTML - Web Search

A novel sequence-based approach to localize translocation breakpoints identifies the molecular basis … - Full text - MIT Libraries
MA Nimmakayalu, AL Gotter, TH Shaikh, BS Emanuel - Human Molecular Genetics, 2003 - hmg.oupjournals.org
... of t(17;22)(q11.2;q11.2) is not consistent with NF1 gene duplication. ... Y., Wilroy,
RS, Jr, Martens, PR and Tharapel, AT (2000) Localization of SRY by primed in ...
Cited by 4 - Web Search - hmg.oupjournals.org - ingentaconnect.com - ncbi.nlm.nih.gov - all 5 versions »

Evidence that Leydig cells in Sertoli-Leydig cell tumors have a reactive rather than a neoplastic …
EE Mooney, YG Man, GL Bratthauer, FA Tavassoli - Cancer, 1999 - doi.wiley.com
... (SRY). ... D3S1300 3p14.2 217–241 4 D16S504 16q24.1 268–284 5 TPOpter-2 2pter 106–130
6 D17S785 17q24 181–207 7 D11S1818 11q22-23 142–158 8 NF1 17q11 171 ...
Cited by 6 - Web Search - doi.wiley.com - ncbi.nlm.nih.gov - Get it from MIT Libraries

Array-based comparative genomic hybridization for the detection of DNA sequence copy number changes … - Full text - MIT Libraries
B Albrecht, M Hausmann, H Zitzelsberger, H Stein, … - The Journal of Pathology, 2004 - doi.wiley.com
... D17S125,D17S61 D17S1296,D17S1523 LLGL1 FLI,TOP3A NF1 5' NF1 3' BRCA1 PPARBP(PBP)
ERBB2 ... exon 45-51 DXS580 DXS7132 AR 3' XIST OCRL1 EST CDY16c07 SRY AZFa region ...
Cited by 2 - Web Search - ingentaconnect.com - ncbi.nlm.nih.gov

A statistical analysis of the TRANSFAC database.
GB Fogel, DG Weekes, G Varga, ER Dow, AM Craven, … - Biosystems, 2005 - natural-selection.com
... MEF-2 MINI20 B Muscle initiator sequence-20 MUSCLE INI B Muscle initiator NF1 Q6
Nuclear ... identified in lymphoid B-cells S8 01 S8 SOX9 B1 SOX (SRY-related HMG ...
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Neuropathology of paediatric chronic intestinal pseudo-obstruction and related animal models - Full text - MIT Libraries
RP Kapur - The Journal of Pathology, 2001 - doi.wiley.com
... Gastrointestinal problems, including CIP, occur in as many as 25% of patients in
the autosomal dominant disorder neurofibromatosis type 1 (NF1) [67]. ...
Cited by 1 - Web Search - doi.wiley.com - ingentaconnect.com - ncbi.nlm.nih.gov - all 5 versions »

Distribution of gamma satellite DNA on the human X and Y chromosomes suggests that it is not … - Full text - MIT Libraries
C Lee, R Critcher, JG Zhang, W Mills, CJ Farr - Chromosoma, 2000 - springerlink.com
... b Chromatin fibres from the human cell line NF1. ... 535 Stevanovic M, Lovell-Badge R,
Collignon J, Goodfellow PN (1993) SOX3 is an X-linked gene related to SRY. ...
Cited by 5 - Web Search - ncbi.nlm.nih.gov - ncbi.nlm.nih.gov

Pre-mRNA splicing modulations in senescence - Full text - MIT Libraries
E Meshorer, H Soreq - Aging Cell, 2002 - blackwell-synergy.com
... CrossRef Abstract MEDLINE Abstract ISI Abstract. • Ohe K, Lalli E, Sassone-Corsi
P (2002) A direct role of SRY and SOX proteins in pre-mRNA splicing. Proc. ...
Cited by 3 - Web Search - ingentaconnect.com - ebi.ac.uk - ncbi.nlm.nih.gov - all 5 versions »

Induction of the Human Papillomavirus Type 31 Late Promoter Requires Differentiation but Not DNA … - Full text - MIT Libraries
KM Spink, LA Laimins - J Virol, 2005 - jvi.asm.org
... for the same subset of factors, including AP1, C/EBPß, NF1, Oct1, Sp1 ... potential
transcription factor binding sites for Oct-1, SOX5, and SRY were identified ...
Web Search - pubmedcentral.nih.gov - jvi.asm.org - ncbi.nlm.nih.gov

Characterization of the human renal Na-sulphate cotransporter gene (NAS1) promoter
ALD Markovich - springerlink.com
... Sox-5: sex- determining region on the Y chromosome (SRY)-related high mobility group
(HMG) box-5 . Sp-1: specificity factor-1 . TFII: transcription factor-II . ...
Web Search - uq.edu.au

Animal models for human contiguous gene syndromes and other genomic disorders - Full text - MIT Libraries
K Walz, P Fonseca, JR Lupski - Genetics and Molecular Biology, 2004 - scielo.br
... SMS: Smith Magenis Syndrome, CMTA1: Charcot-Marie-Tooth Disease, HNPP: Hereditary
Neuropathy with Liability to Pressure Palsies, NF1: Neuro- fibromatosis I, AGS ...
View as HTML - Web Search - scielo.br

The chicken telomerase RNA gene: conservation of sequence, regulatory elements and synteny among … - Full text - MIT Libraries
ME Delany, LM Daniels, FTC Alert - Cytogenetic and Genome Research, 2003 - content.karger.com
... c-Ets-1 0 1 -464 0 1 -473 2 -73, -53 NF1 0 0 1 -253 2 -576, -183 1 -89 SRY 0 0 0
2 -580, -382 1 -521 c-Jun 0 0 1 -524 f 3 -520 f , -89 f , -70 f 0 ...
Cited by 2 - Web Search - dx.doi.org - karger.com - ncbi.nlm.nih.gov - all 5 versions »

Structural organization and classification of the human mucin genes
N Moniaux, F Escande, N Porchet, JP Aubert, SK … - Front Biosci, 2001 - xylian.igh.cnrs.fr
... Other elements found are boxes that bind AP1, AP2, AP3, AP4, CTF/NF1, ER, PR, Sp1,
STAT1 ... 1, Ikaros, IL-6 RE, LyF1, NF-GMCSF, NF-mu-E1, NF-Y, Pu-box, SRY, TCF-1 ...
Cited by 57 - Cached - Web Search - bioscience.org - bioscience.org - ncbi.nlm.nih.gov - all 7 versions » - Get it from MIT Libraries

Integrated Program Suite for Tension Structure Design
T Limited - tensys.com
Page 1. TENSYS TENSION STRUCTURES ENGINEERING Tensys Limited 1 St Swithins
Yard Walcot Street Bath BA1 5BG UK T +44 (0)1225 321950 ...
Web Search - tensys.com

Cloning of translocation breakpoints associated with Shwachman syndrome and identification of a … - Full text - MIT Libraries
S Ikegawa, M Masuno, Y Kumano, A Okawa, M Isomura, … - Clinical Genetics, 1999 - blackwell-synergy.com
... A, Danglot G. Emergence and scattering of multiple neurofibromatosis (NF1)-related
sequences ... are caused by mutations in and around the SRY-related gene SOX9. ...
Cited by 7 - Web Search - ncbi.nlm.nih.gov

Generation of Two Distinct Functional Isoforms of DAX-1 by Alternative Splicing - Full text - MIT Libraries
A HOSSAIN, C LI, GF SAUNDERS - Molecular Endocrinology, 2004 - mend.endojournals.org
... CCAAT/enhancer binding protein), and ubiquitous transcription factors NF1 (nuclear
factor 1 ... P, Camerino G, Lovell-Badge R 1998 Dax1 antagonizes Sry action in ...
Web Search - mend.endojournals.org

Highly conserved proximal promoter element harboring paired Sox9-binding sites contributes to the … - Full text - MIT Libraries
O Rentsendorj, A Nagy, I Sinko, A Daraba, E Barta, … - Biochem J, 2005 - biochemj.org
... mobility-group (HMG) box DNA-binding domain highly similar to that of Sry,
a mammalian testis-determining factor [10- 11]. HMG box ...
View as HTML - Web Search - biochemj.org - ncbi.nlm.nih.gov

Pax3 and the splotch mutations: structure, function, and relationship to teratogenesis, including …
AF Machado, LJ Martin, MD Collins - Curr. Pharm. Design, 2001 - ingentaconnect.com
Page 1. Current Pharmaceutical Design, 2001, 7, 751-785 751 Pax3 and the
Splotch Mutations: Structure, Function, and Relationship to ...
Cited by 7 - Web Search - bentham.org - bentham.org - ncbi.nlm.nih.gov - Get it from MIT Libraries

Generation of Two Distinct Functional Isoforms of Dosage-Sensitive Sex Reversal-Adrenal Hypoplasia … - Full text - MIT Libraries
A Hossain, C Li, GF Saunders - Mol Endocrinol, 2004 - mend.endojournals.org
... EBPß (CCAAT/enhancer binding protein), and ubiquitous transcription factors NF1
(nuclear factor ... Camerino G, Lovell-Badge R 1998 Dax1 antagonizes Sry action in ...
Cited by 3 - Web Search - dx.doi.org - mend.endojournals.org - ncbi.nlm.nih.gov - all 5 versions »