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Gardella
R, Zoppi N, Assanelli D, Muiesan ML, Barlati S, Colombi M.
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Exclusion
of candidate
genes in a family with arterial tortuosity syndrome
Am J Med Genet 2003 (in stampa)
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| Coucke
PJ, Wessels MW, Van Acker P, Gardella R, Barlati
S, Willems PJ, Colombi M, De Paepe A. |
Related
Articles |
Homozygosity mapping of a gene for
arterial tortuosity syndrome to chromosome 20q13.
J Med Genet. 2003 Oct;40(10):747-751.
PMID: 14569121 [PubMed - as supplied by publisher] |
|
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| Barbon
A, Vallini I, La Via L, Marchina E, Barlati S. |
Related
Articles |
Glutamate receptor RNA editing: a
molecular analysis of GluR2, GluR5
and GluR6 in human brain tissues and in NT2 cells following in vitro
neural differentiation.
Brain Res Mol Brain Res. 2003 Oct 7;117(2):168-78.
PMID: 14559151
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| Fumagalli
F, Bedogni F, Maragnoli ME, Gennarelli M, Perez J, Racagni G, Riva MA. |
Related
Articles |
Dopaminergic
D2 receptor activation modulates FGF-2 gene expression in rat
prefrontal cortex and hippocampus.
J Neurosci Res. 2003 Oct
1;74(1):74-80.
PMID: 13130508 |
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| Seripa
D, Forno GD, Matera MG, Gravina C, Margaglione M, Palermo MT, Wekstein
DR, Antuono P, Davis DG, Daniele A, Masullo C, Bizzarro A, Gennarelli
M, Fazio VM. |
Related
Articles |
Methylenetetrahydrofolate
reductase and angiotensin converting enzyme
gene polymorphisms in two genetically and diagnostically distinct
cohort of Alzheimer patients.
Neurobiol Aging. 2003
Nov;24(7):933-9.
PMID: 12928053 |
|
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| Fumagalli
F, Molteni R, Roceri M, Bedogni F, Santero R, Fossati C, Gennarelli M,
Racagni G, Riva MA. |
Related
Articles |
Effect
of antipsychotic drugs on brain-derived neurotrophic factor
expression under reduced N-methyl-D-aspartate receptor activity.
J Neurosci Res. 2003 Jun
1;72(5):622-8.
PMID: 12749027 |
|
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| Celano
E, Tiraboschi E, Consogno E, D'Urso G, Mbakop MP, Gennarelli M, de
Bartolomeis A, Racagni G, Popoli M. |
Related
Articles |
Selective
regulation of presynaptic calcium/calmodulin-dependent protein kinase
II by psychotropic drugs.
Biol Psychiatry. 2003 Mar
1;53(5):442-9.
PMID: 12614997 |
|
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| De
Luca A, Conti E, Grifone N, Amati F, Spalletta G, Caltagirone C,
Bonaviri G, Pasini A, Gennarelli M, Stefano B, Berti L, Mittler G,
Meisterernst M, Dallapiccola B, Novelli G. |
Related
Articles |
Association
study between CAG trinucleotide repeats in the PCQAP gene
(PC2 glutamine/Q-rich-associated protein) and schizophrenia.
Am J Med Genet. 2003 Jan
1;116B(1):32-5.
PMID: 12497610 |
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| Izzi
C, Barbon
A,Toliat MR,Heils A, Becker C, Nürnberg P, Sander T and S Barlati. |
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Candidate gene analysis of the human
metabotropic
glutamate receptor type 4 (GRM4) in patients with juvenile myoclonic
epilepsy.
Am J Med Genet. 2003 Nov 15;123B(1):59-63.
PMID: 14582146 [PubMed - in process] |
|
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| Begni
S, Moraschi S, Bignotti S, Fumagalli F, Rillosi
L, Perez J, Gennarelli M. |
Related
Articles |
Association
between the
G1001C polymorphism in the GRIN1 gene promoter region and schizophrenia.
Biol Psychiatry. 2003
Apr 1;53(7):617-9.
PMID: 12679240 |
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| Colombi
M, Zoppi N, De Petro G, Marchina E, Gardella R, Tavian D, Ferraboli S,
Barlati S. |
Related
Articles |
Matrix
assembly induction and cell migration and invasion inhibition by a
13-amino acid fibronectin peptide.
J Biol Chem. 2003 Apr
18;278(16):14346-55. Epub 2003 Feb 11.
PMID: 12582155 |
|
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| Tavian
D, Salvi A, De Petro G, Barlati S. |
Related
Articles |
Stable
expression of antisense urokinase mRNA inhibits the proliferation and
invasion of human hepatocellular carcinoma cells.
Cancer Gene Ther.
2003
Feb;10(2):112-20.
PMID: 12536199 |
|
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| Ferrari
M, Scalvini A, Losio MN, Corradi A, Soncini M, Bignotti E, Milanesi E,
Ajmone-Marsan P, Barlati S, Bellotti D, Tonelli M. |
Related
Articles |
Establishment
and characterization of two new pig cell lines for use in virological
diagnostic laboratories.
J Virol Methods.
2003
Feb;107(2):205-12.
PMID: 12505635 |
|
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| Popoli
M, Gennarelli M, Racagni G. |
Related
Articles |
Modulation
of synaptic plasticity by stress and antidepressants.
Bipolar Disord.
2002
Jun;4(3):166-82. Review.
PMID: 12180272 |
|
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| Begni
S, Popoli M, Moraschi S, Bignotti S, Tura GB, Gennarelli M. |
Related
Articles |
Association
between the ionotropic glutamate receptor kainate 3 (GRIK3) ser310ala
polymorphism and schizophrenia.
Mol Psychiatry.
2002;7(4):416-8.
PMID: 11986986 |
|
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| Chiavetto
LB, Boin F, Zanardini R, Popoli M, Michelato A, Bignotti S, Tura GB,
Gennarelli M. |
Related
Articles |
Association
between promoter polymorphic haplotypes of interleukin-10 gene and
schizophrenia.
Biol Psychiatry. 2002
Mar
15;51(6):480-4.
PMID: 11922883 |
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| Ventriglia
M, Bocchio Chiavetto L, Benussi L, Binetti G, Zanetti O, Riva MA,
Gennarelli M. |
Related
Articles |
Association
between the
BDNF 196 A/G polymorphism and sporadic Alzheimer's disease.
Mol Psychiatry. 2002;7(2):136-7. No abstract available.
PMID: 11840305
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| Ventriglia
M, Bocchio Chiavetto L, Bonvicini C, Tura GB, Bignotti S, Racagni G,
Gennarelli M. |
Related
Articles |
Allelic
variation in the human prodynorphin gene promoter and schizophrenia.
Neuropsychobiology.
2002;46(1):17-21.
PMID: 12207142 |
|
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| Monti
E, Preti A, Venerando B, Borsani G. |
Related
Articles |
Recent
development in mammalian sialidase molecular biology.
Neurochem Res. 2002
Aug;27(7-8):649-63. Review.
PMID: 12374200 |
|
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| Gardella
R, Castiglia D, Posteraro P, Bernardini S, Zoppi N, Paradisi M, Tadini
G, Barlati S, McGrath JA, Zambruno G, Colombi M. |
Related
Articles |
Genotype-phenotype
correlation in italian patients with dystrophic epidermolysis bullosa.
J Invest Dermatol. 2002
Dec;119(6):1456-62.
PMID: 12485454 |
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| Tavian
D, De Petro G, Pitozzi A, Portolani N, Giulini SM, Barlati S. |
Related
Articles |
Androgen
receptor mRNA under-expression in poorly differentiated human
hepatocellular carcinoma.
Histol
Histopathol. 2002
Oct;17(4):1113-9.
PMID: 12371139 |
|
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| Gardella
R, Zoppi N, Zambruno G, Barlati S, Colombi M. |
Related
Articles |
Different
phenotypes in recessive dystrophic epidermolysis bullosa
patients sharing the same mutation in compound heterozygosity with two
novel mutations in the type VII collagen gene.
Br J Dermatol.
2002
Sep;147(3):450-7.
PMID: 12207583 |
|
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| De
Petro G, Tavian D, Marchina E, Barlati S. |
Related
Articles |
Induction
of fibronectin mRNA by urokinase- and
tissue-type plasminogen activator in human skin fibroblasts:
differential role of u-PA and t-PA at the fibronectin protein level.
Biol Chem. 2002
Jan;383(1):177-87.
PMID: 11928812 |
|
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| Izzi
C, Barbon A, Kretz R, Sander T, Barlati S. |
Related
Articles |
Sequencing
of the GRIK1 gene in patients with juvenile absence epilepsy does not
reveal mutations affecting receptor structure.
Am J Med Genet.
2002 Apr
8;114(3):354-9.
PMID: 11920863 |
|
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| Ballmaier
M, Zoli M, Mazzoncini R, Gennarelli M, Spano F. |
Related
Articles |
Combined
alpha 2-adrenergic/D2 dopamine receptor blockade fails to
reproduce the ability of clozapine to reverse phencyclidine-induced
deficits in prepulse inhibition of startle.
Psychopharmacology
(Berl). 2001
Dec;159(1):105-10. Epub 2001 Sep 11.
PMID: 11797077 |
|
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| Gardella
R, Nuytinck L, Barlati S, Van Acker P, Tadini G, De Paepe A, Colombi M. |
Related
Articles |
Characterization
of mutations leading to recessive dystrophic epidermolysis bullosa and
Marfan syndrome in a single patient.
Clin Exp
Dermatol. 2001
Nov;26(8):710-3.
PMID: 11722462 |
|
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| Valerio
A, Zoppi N, Ferraboli S, Paterlini M, Ferrario M, Barlati S, Spano P. |
Related
Articles |
Alternative splicing of mGlu6 gene generates a truncated glutamate
receptor in rat retina.
Neuroreport. 2001
Aug 28;12(12):2711-5.
PMID: 11522953
|
|
|
| Barbon
A, Vallini I, Barlati S. |
Related
Articles |
Genomic organization of the human GRIK2 gene and evidence for multiple
splicing variants.
Gene. 2001 Aug
22;274(1-2):187-97.
PMID: 11675011
|
|
|
| Palacin
M, Borsani G, Sebastio G. |
Related
Articles |
The
molecular bases of cystinuria and lysinuric protein intolerance.
Curr Opin Genet Dev. 2001
Jun;11(3):328-35. Review.
PMID: 11377971 |
|
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| Bassi
MT, Gasol E, Manzoni M, Pineda M, Riboni M, Martin R, Zorzano A,
Borsani G, Palacin M. |
Related
Articles |
Identification
and characterisation of human xCT that
co-expresses, with 4F2 heavy chain, the amino acid transport activity
system xc-.
Pflugers Arch. 2001
May;442(2):286-96.
PMID: 11417227 |
|
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| Font
MA, Feliubadalo L, Estivill X, Nunes V, Golomb E, Kreiss Y, Pras E,
Bisceglia L, d'Adamo AP, Zelante L, Gasparini P, Bassi MT, George AL
Jr, Manzoni M, Riboni M, Ballabio A, Borsani G, Reig N, Fernandez E,
Zorzano A, Bertran J, Palacin M; International Cystinuria Consortium. |
Related
Articles |
Functional
analysis of mutations in SLC7A9, and genotype-phenotype correlation in
non-Type I cystinuria.
Hum Mol Genet. 2001 Feb
15;10(4):305-16.
PMID: 11157794 |
|
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| Popoli
M, Mori S, Brunello N, Perez J, Gennarelli M, Racagni G. |
Related
Articles |
Serine/threonine
kinases as molecular targets of
antidepressants: implications for pharmacological treatment and
pathophysiology of affective disorders.
Pharmacol Ther. 2001
Feb;89(2):149-70. Review.
PMID: 11316518
|
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| Siciliano
G, Manca M, Gennarelli M, Angelini C, Rocchi A, Iudice A, Miorin M,
Mostacciuolo M. |
Related
Articles |
Epidemiology
of myotonic dystrophy in Italy: re-apprisal after genetic diagnosis.
Clin Genet. 2001
May;59(5):344-9.
PMID: 11359466 |
|
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| Fumagalli
F, Santero R, Gennarelli M, Giorgio Racagni, Andrea Riva M. |
Related
Articles |
Decreased
hippocampal BDNF expression after acute systemic injection of
quinpirole.
Neuropharmacology. 2001
Jun;40(7):954-7.
PMID: 11378166 |
|
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| Tascedda
F, Blom JM, Brunello N, Zolin K, Gennarelli M, Colzi A, Bravi D, Carra
S, Racagni G, Riva MA. |
Related
Articles |
Modulation
of glutamate receptors in response to the novel antipsychotic
olanzapine in rats.
Biol Psychiatry. 2001 Jul
15;50(2):117-22.
PMID: 11526992
|
|
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| Consogno
E, Tiraboschi E, Iuliano E, Gennarelli M, Racagni G, Popoli M. |
Related
Articles |
Long-term
treatment with S-adenosylmethionine induces changes in presynaptic CaM
kinase II and synapsin I.
Biol Psychiatry. 2001 Sep
1;50(5):337-44.
PMID: 11543736 |
|
|
| Scozzari
R, Cruciani F, Pangrazio A, Santolamazza P, Vona G, Moral P, Latini V,
Varesi L, Memmi MM, Romano V, De Leo G, Gennarelli M, Jaruzelska J,
Villems R, Parik J, Macaulay V, Torroni A. |
Related
Articles |
Human
Y-chromosome variation in the western Mediterranean area: implications
for the peopling of the region.
Hum Immunol. 2001
Sep;62(9):871-84.
PMID: 11543889 |
|
|
| Molteni
R, Fumagalli F, Magnaghi V, Roceri M, Gennarelli M, Racagni G, Melcangi
RC, Riva MA. |
Related
Articles |
Modulation
of fibroblast growth factor-2 by stress and corticosteroids: from
developmental events to adult brain plasticity.
Brain Res Brain Res Rev. 2001
Nov;37(1-3):249-58. Review.
PMID: 11744090 |
|
|
| Boin
F, Zanardini R, Pioli R, Altamura CA, Maes M, Gennarelli M. |
Related
Articles |
Association
between -G308A tumor necrosis factor alpha gene polymorphism and
schizophrenia.
Mol Psychiatry. 2001
Jan;6(1):79-82.
PMID: 11244489 |
|
|
| Roceri
M, Molteni R, Fumagalli F, Racagni G, Gennarelli M, Corsini G, Maggio
R, Riva M. |
Related
Articles |
Stimulatory
role of dopamine on fibroblast growth factor-2 expression in rat
striatum.
J Neurochem. 2001
Feb;76(4):990-7.
PMID: 11181818
|
|
|
Valerio
A, Ferraboli S, Paterlini M,
Spano P, Barlati S.
|
Related
Articles |
Identification
of novel alternatively-spliced mRNA isoforms of metabotropic glutamate
receptor 6 gene in rat and human retina.
Gene. 2001 Jan
10;262(1-2):99-106.
PMID: 11179672
|
|
|
| Bassi
MT, Manzoni M, Monti E, Pizzo MT, Ballabio A, Borsani G. |
Related
Articles |
Cloning
of the gene encoding a novel integral membrane protein,
mucolipidin-and identification of the two major founder mutations
causing mucolipidosis type IV.
Am J Hum Genet. 2000
Nov;67(5):1110-20. Epub 2000 Sep 29.
PMID: 11013137 |
|
|
| Monti
E, Bassi MT, Papini N, Riboni M,
Manzoni M, Venerando B, Croci G, Preti A, Ballabio A, Tettamanti G,
Borsani G. |
Related
Articles |
Identification and expression of NEU3, a
novel human sialidase associated to the plasma membrane.
Biochem J. 2000 Jul
1;349(Pt 1):343-51.
PMID: 10861246
|
|
|
| Gardella
R, Barlati S, Zoppi N, Tadini
G, Colombi M. |
Related
Articles |
A -96C-->T mutation in the promoter of the collagen type VII gene
(COL7A1) abolishing transcription in a patient affected by recessive
dystrophic epidermolysis bullosa.
Hum Mutat. 2000 Sep;16(3):275.
[MEDLINE record in process]
PMID: 10980546; UI: 20438362
|
|
|
| Tavian
D, De Petro G, Benetti A,
Portolani N, Giulini
SM, Barlati S. |
Related
Articles |
u-PA and c-MET mRNA expression is co-ordinately enhanced while
hepatocyte growth factor mRNA is down-regulated in human hepatocellular
carcinoma.
Int J Cancer. 2000 Sep 1;87(5):644-9.
PMID: 10925356; UI: 20384682
|
|
|
| Barbon
A, Ferraboli S, Barlati S. |
Related
Articles |
Assignment of the human metabotropic glutamate receptor gene GRM7 to
chromosome 3p26.1-->p25.2 by radiation hybrid mapping.
Cytogenet Cell Genet. 2000;88(3-4):288. No abstract available.
PMID: 10828612; UI: 20291012
|
|
|
| Barbon
A, Barlati S. |
Related Articles, Protein,
Nucleotide |
Genomic organization, proposed alternative splicing mechanisms, and RNA
editing structure of GRIK1.
Cytogenet Cell Genet. 2000;88(3-4):236-9.
PMID: 10828597; UI: 20290997
|
|
|
| Barbon
A, Ferraboli S, Barlati S. |
Realted
Articles
|
Assignment of the human metabotropic glutamate receptor gene GRM4 to
chromosome 6 band p21.3 by radiation hybrid mapping.
Cytogenet Cell Genet. 2000;88(3-4):210. No abstract available.
PMID: 10828590; UI: 20290990
|
|
|
| Copeta
A, Tavian D, Marchina E, De
Petro G, Barlati S. |
Related
Articles |
Gene response of
human skin fibroblasts to urokinase- and tissue-type
plasminogen activators.
Growth Factors. 2000;17(4):249-68.
PMID: 10801075; UI: 20259013
|
|
|
| Rossi
G, Pelizzari AM, Bellotti D, Tonelli M, Barlati S. |
Related
Articles |
Cytogenetic
analogy between myelodysplastic syndrome and acute myeloid
leukemia of elderly patients.
Leukemia. 2000 Apr;14(4):636-41.
PMID: 10764149; UI: 20225219
|
|
|
| De
Grandi A, Calvari V, Bertini V, Bulfone A, Peverali G, Camerino G,
Borsani G, Guioli S. |
Related
Articles |
The
expression pattern of a mouse doublesex-related gene is consistent with
a role in gonadal differentiation.
Mech Dev. 2000 Feb;90(2):323-6.
PMID: 10640721 |
|
|
| Sperandeo
MP, Bassi MT, Riboni M, Parenti G, Buoninconti A, Manzoni M, Incerti B,
Larocca MR, Di Rocco M, Strisciuglio P, Dianzani I, Parini R, Candito
M, Endo F, Ballabio A, Andria G, Sebastio G, Borsani G. |
Related
Articles |
Structure
of the SLC7A7 gene and mutational analysis of patients affected by
lysinuric protein intolerance.
Am J Hum Genet. 2000
Jan;66(1):92-9.
PMID: 10631139 |
|
|
| De
Panfilis G, Ghidini A, Graifemberghi S, Barlati S,
Zoppi N, Colombi M. |
Related
Articles |
Dexamethasone-induced healing of chronic leg ulcers in a patient with
defective organization of the extracellular matrix of fibronectin.
Br J Dermatol. 2000 Jan;142(1):166-70.
PMID: 10651716; UI: 20117435
|
|
|
| Amicucci
P, Gennarelli M, Novelli G, Dallapiccola B. |
Related
Articles |
Prenatal
diagnosis of myotonic dystrophy using fetal DNA obtained from maternal
plasma.
Clin Chem. 2000
Feb;46(2):301-2. No abstract available.
PMID: 10657396 |
|
|
| Antonini
G, Giubilei F, Mammarella A, Amicucci P, Fiorelli M, Gragnani F, Morino
S, Ceschin PV, Fragola PV, Gennarelli M. |
Related
Articles |
Natural
history of cardiac involvement in myotonic dystrophy: correlation with
CTG repeats.
Neurology. 2000 Oct
24;55(8):1207-9.
PMID: 11071501 |
|
|
| Barlati
S, Zoppi N, Copeta A, Tavian D, De Petro G,
Colombi M. |
Related
Articles |
Quantitative in situ hybridization for the evaluation of gene
expression in asynchronous and synchronized cell cultures and in tissue
sections.
Histol Histopathol. 1999 Oct;14(4):1231-40. Review.
PMID: 10506939; UI: 99436827
|
|
|
| Gardella
R, Zoppi N, Ferraboli S, Marini D, Tadini G,
Barlati S, Colombi M. |
Related
Articles |
Three
homozygous PTC mutations in the collagen type VII gene of
patients affected by recessive dystrophic epidermolysis bullosa:
analysis of transcript levels in dermal fibroblasts.
Hum Mutat. 1999;13(6):439-52.
PMID: 10408773; UI: 99335258
|
|
|
| Bassi
MT, Sperandeo MP, Incerti B, Bulfone A, Pepe A, Surace EM, Gattuso C,
De Grandi A, Buoninconti A, Riboni M, Manzoni M, Andria G, Ballabio A,
Borsani G, Sebastio G. |
Related
Articles |
SLC7A8,
a gene mapping within the lysinuric protein intolerance
critical region, encodes a new member of the glycoprotein-associated
amino acid transporter family.
Genomics. 1999 Dec
1;62(2):297-303.
PMID: 10610726
|
|
|
| Monti
E, Preti A, Nesti C, Ballabio A, Borsani G. |
Related
Articles |
Expression
of a novel human sialidase encoded by the NEU2 gene.
Glycobiology. 1999
Dec;9(12):1313-21.
PMID: 10561456 |
|
|
| Feliubadalo
L, Font M, Purroy J, Rousaud F, Estivill X, Nunes V, Golomb E, Centola
M, Aksentijevich I, Kreiss Y, Goldman B, Pras M, Kastner DL, Pras E,
Gasparini P, Bisceglia L, Beccia E, Gallucci M, de Sanctis L, Ponzone
A, Rizzoni GF, Zelante L, Bassi MT, George AL Jr, Palacin M, et al. |
Related
Articles |
Non-type
I cystinuria caused by mutations in SLC7A9, encoding a subunit (bo,+AT)
of rBAT. International Cystinuria Consortium.
Nat Genet. 1999 Sep;23(1):52-7.
PMID: 10471498 |
|
|
| Barbieri
AM, Lupo G, Bulfone A, Andreazzoli M, Mariani M, Fougerousse F,
Consalez GG, Borsani G, Beckmann JS, Barsacchi G, Ballabio A, Banfi S. |
Related
Articles |
A
homeobox gene, vax2, controls the patterning of the eye dorsoventral
axis.
Proc Natl Acad Sci U S A. 1999
Sep 14;96(19):10729-34.
PMID: 10485894 |
|
|
| Bassi
MT, Ramesar RS, Caciotti B, Winship IM, De Grandi A, Riboni M, Townes
PL, Beighton P, Ballabio A, Borsani G. |
Related
Articles |
X-linked
late-onset sensorineural deafness caused by a deletion involving OA1
and a novel gene containing WD-40 repeats.
Am J Hum Genet. 1999
Jun;64(6):1604-16.
PMID: 10330347 |
|
|
| Monti
E, Preti A, Rossi E, Ballabio A, Borsani G. |
Related
Articles |
Cloning
and characterization of NEU2, a human gene homologous to rodent soluble
sialidases.
Genomics. 1999 Apr
1;57(1):137-43.
PMID: 10191093 |
|
|
| Lavorgna
G, Guffanti A, Borsani G, Ballabio A, Boncinelli E. |
Related
Articles |
TargetFinder:
searching annotated sequence databases for target genes of
transcription factors.
Bioinformatics. 1999
Feb;15(2):172-3.
PMID: 10089203 |
|
|
| Borsani
G, Bassi MT, Sperandeo MP, De Grandi A, Buoninconti A, Riboni M,
Manzoni M, Incerti B, Pepe A, Andria G, Ballabio A, Sebastio G. |
Related
Articles |
SLC7A7,
encoding a putative permease-related protein, is mutated in patients
with lysinuric protein intolerance.
Nat Genet. 1999
Mar;21(3):297-301.
PMID: 10080183 |
|
|
| Borsani
G, DeGrandi A, Ballabio A, Bulfone A, Bernard L, Banfi S, Gattuso C,
Mariani M, Dixon M, Donnai D, Metcalfe K, Winter R, Robertson M, Axton
R, Brown A, van Heyningen V, Hanson I. |
Related
Articles |
EYA4,
a novel vertebrate gene related to Drosophila eyes absent.
Hum Mol Genet. 1999
Jan;8(1):11-23.
PMID: 9887327 |
|
|
| Korade-Mirnics
Z, Tarleton J, Servidei S, Casey RR, Gennarelli M, Pegoraro E, Angelini
C, Hoffman EP. |
Related
Articles |
Myotonic
dystrophy: tissue-specific effect of somatic CTG expansions on
allele-specific DMAHP/SIX5 expression.
Hum Mol Genet. 1999
Jun;8(6):1017-23.
PMID: 10332033
|
|
|
| Gennarelli
M, Pavoni M, Amicucci P, Angelini C, Menegazzo E, Zelano G, Novelli G,
Dallapiccola B. |
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Reduction
of the DM-associated homeo domain protein (DMAHP) mRNA in different
brain areas of myotonic dystrophy patients.
Neuromuscul Disord. 1999
Jun;9(4):215-9.
PMID: 10399747
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|
|
| Perini
GI, Menegazzo E, Ermani M, Zara M, Gemma A, Ferruzza E, Gennarelli M,
Angelini C. |
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Cognitive
impairment and (CTG)n expansion in myotonic dystrophy patients.
Biol Psychiatry. 1999 Aug
1;46(3):425-31.
PMID: 10435210
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| Gennarelli
M, Pavoni M, Cruciani F, De Stefano G, Dallapiccola B, Novelli G. |
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CTG
repeats distribution and Alu insertion polymorphism at myotonic
dystrophy (DM) gene in Amhara and Oromo populations of Ethiopia.
Hum Genet. 1999
Jul-Aug;105(1-2):165-7.
PMID: 10480373
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| Servidei
S, Capon F, Spinazzola A, Mirabella M, Semprini S, de Rosa G,
Gennarelli M, Sangiuolo F, Ricci E, Mohrenweiser HW, Dallapiccola B,
Tonali P, Novelli G. |
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A
distinctive autosomal dominant vacuolar neuromyopathy linked to 19p13.
Neurology. 1999 Sep
11;53(4):830-7.
PMID: 10489050
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| Volorio
S, Simon G, Repetto M, Cucciardi M, Banfi S,
Borsani G, Ballabio A, Zollo M. |
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Sequencing
analysis of forty-eight human image cDNA clones similar to Drosophila
mutant protein.
DNA Seq. 1998;9(5-6):307-15.
PMID: 10524757 |
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| Nisoli
E, Carruba MO, Valerio A, Borsani G. |
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Hypocretins or hyporexins?
Nat Med. 1998 Jun;4(6):645. No abstract available.
PMID: 9623954 |
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| Gennarelli
M, Pavoni M, Amicucci P, Novelli G, Dallapiccola B. |
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A single polymerase chain
reaction-based protocol
for detecting normal and expanded alleles in myotonic dystrophy.
Diagn Mol Pathol. 1998
Jun;7(3):135-7.
PMID: 9836067 |
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| Marcon
M, Briani C, Ermani M, Menegazzo E, Iurilli V, Feltrin GP, Novelli G,
Gennarelli M, Angelini C. |
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Positive correlation of CTG expansion
and
pharyngoesophageal alterations in myotonic dystrophy patients.
Ital J Neurol Sci. 1998
Apr;19(2):75-80.
PMID: 10935840 |
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| Gennarelli
M, Lucarelli M, Amicucci P, Soddu S, Novelli G, Dallapiccola B. |
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Genomic instability associated with
myotonic
dystrophy does not involve p53 expression and activity.
Cell Biochem Funct. 1998
Jun;16(2):117-22.
PMID: 9636999 |
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| Torrente
I, Mangino M, De Luca A, Mingarelli R,
Gennarelli M, Giannotti A, Novelli G, Dallapiccola B. |
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First-trimester prenatal diagnosis of
Ellis-van Creveld syndrome using linked microsatellite markers.
Prenat Diagn. 1998 May;18(5):504-6.
PMID: 9621386 |
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| Zoppi
N, Ghinelli A, Gardella R, Barlati S, Colombi M. |
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Effect of dexamethasone on the assembly of the matrix of fibronectin
and on its receptors organization in Ehlers-Danlos syndrome skin
fibroblasts.
Cell Biol Int. 1998;22(7-8):499-508.
PMID: 10452818; UI: 99386761
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|
| Bulfone
A, Gattuso C, Marchitiello A, Pardini C,
Boncinelli E, Borsani G, Banfi S, Ballabio A. |
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The embryonic expression pattern of 40 murine cDNAs homologous to
Drosophila mutant genes (Dres): a comparative and topographic approach
to predict gene function.
Hum Mol Genet. 1998 Dec;7(13):1997-2006.
PMID: 9817915
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|
| Borsani
G, Ballabio A, Banfi S. |
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A practical guide to orient yourself in the labyrinth of
genome databases.
Hum Mol Genet. 1998;7(10):1641-8. Review.
PMID: 9735386
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|
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| de
Conciliis L, Marchitiello A, Wapenaar MC, Borsani G, Giglio S, Mariani
M, Consalez GG, Zuffardi O, Franco B, Ballabio A, Banfi S. |
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Characterization of Cxorf5 (71-7A), a
novel human cDNA mapping to Xp22
and encoding a protein containing coiled-coil alpha-helical domains.
Genomics. 1998 Jul 15;51(2):243-50.
PMID: 9722947 |
|
|
| De
Petro G, Tavian D, Copeta A, Portolani N, Giulini
SM, Barlati S. |
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Expression of urokinase-type plasminogen activator (u-PA), u-PA
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carcinoma.
Cancer Res. 1998 May 15;58(10):2234-9.
PMID: 9605771; UI: 98266808
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|
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| Sperandeo
MP, Borsani G, Incerti B, Zollo M, Rossi E,
Zuffardi O, Castaldo P, Taglialatela M, Andria G, Sebastio G |
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The
gene encoding a
cationic amino acid transporter (SLC7A4) maps to the region deleted in
the velocardiofacial syndrome.
Genomics. 1998 Apr 15;49(2):230-6.
PMID: 9598310 |
|
|
| Banfi
S, Guffanti A, Borsani G. |
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How to get
the best of dbEST.
Trends Genet. 1998 Feb;14(2):80-1. No abstract available.
PMID: 9520602 |
|
|
| Piccini
M, Vitelli F, Bruttini M, Pober BR, Jonsson JJ,
Villanova M, Zollo M, Borsani G, Ballabio A, Renieri A. |
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FACL4, a new gene encoding long-chain acyl-CoA
synthetase 4, is deleted in a family with Alport syndrome,
elliptocytosis, and mental retardation.
Genomics. 1998 Feb 1;47(3):350-8.
PMID: 9480748 |
|
|
| Bione
S, Sala C, Manzini C, Arrigo G, Zuffardi O, Banfi S, Borsani G,
Jonveaux P, Philippe C, Zuccotti M, Ballabio A, Toniolo D. |
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A human homologue of the Drosophila
melanogaster diaphanous gene is
disrupted in a patient with premature ovarian failure: evidence for
conserved function in oogenesis and implications for human sterility.
Am J Hum Genet. 1998 Mar;62(3):533-41.
PMID: 9497258 |
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