Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 32

1.

RNA FISH, DNA FISH and Chromosome Painting of Chicken Oocytes.

Guioli S, Lovell-Badge R.

Methods Mol Biol. 2016;1457:191-208. doi: 10.1007/978-1-4939-3795-0_14.

PMID:
27557582
2.

Gonadal asymmetry and sex determination in birds.

Guioli S, Nandi S, Zhao D, Burgess-Shannon J, Lovell-Badge R, Clinton M.

Sex Dev. 2014;8(5):227-42. doi: 10.1159/000358406. Epub 2014 Feb 27. Review.

3.

Error-prone ZW pairing and no evidence for meiotic sex chromosome inactivation in the chicken germ line.

Guioli S, Lovell-Badge R, Turner JM.

PLoS Genet. 2012;8(3):e1002560. doi: 10.1371/journal.pgen.1002560. Epub 2012 Mar 8.

4.

Meiosis onset is postponed to postnatal stages during ovotestis development in female moles.

Zurita F, Carmona FD, Lupiáñez DG, Barrionuevo FJ, Guioli S, Burgos M, Jiménez R.

Sex Dev. 2007;1(1):66-76. doi: 10.1159/000096240.

5.
6.

The origin of the Mullerian duct in chick and mouse.

Guioli S, Sekido R, Lovell-Badge R.

Dev Biol. 2007 Feb 15;302(2):389-98. Epub 2006 Oct 3.

7.

Proliferation and migration of granule cells in the developing rat cerebellum: cisplatin effects.

Pisu MB, Roda E, Guioli S, Avella D, Bottone MG, Bernocchi G.

Anat Rec A Discov Mol Cell Evol Biol. 2005 Dec;287(2):1226-35.

8.
9.

A new submicroscopic deletion that refines the 9p region for sex reversal.

Calvari V, Bertini V, De Grandi A, Peverali G, Zuffardi O, Ferguson-Smith M, Knudtzon J, Camerino G, Borsani G, Guioli S.

Genomics. 2000 May 1;65(3):203-12.

PMID:
10857744
10.

The expression pattern of a mouse doublesex-related gene is consistent with a role in gonadal differentiation.

De Grandi A, Calvari V, Bertini V, Bulfone A, Peverali G, Camerino G, Borsani G, Guioli S.

Mech Dev. 2000 Feb;90(2):323-6.

11.

Molecular analysis of 9p deletions associated with XY sex reversal: refining the localization of a sex-determining gene to the tip of the chromosome.

Guioli S, Schmitt K, Critcher R, Bouzyk M, Spurr NK, Ogata T, Hoo JJ, Pinsky L, Gimelli G, Pasztor L, Goodfellow PN.

Am J Hum Genet. 1998 Sep;63(3):905-8. No abstract available.

12.

Integrated radiation hybrid and yeast artificial chromosome map of chromosome 9p.

Bouzyk M, Bryant SP, Evans C, Guioli S, Ford S, Schmidt K, Goodfellow PN, Povey S, Rebello M, Rousseaux S, Spurr NK.

Eur J Hum Genet. 1997 Sep-Oct;5(5):299-307.

PMID:
9412787
13.

Campomelic dysplasia with XY sex reversal: diverse phenotypes resulting from mutations in a single gene.

Schafer AJ, Foster JW, Kwok C, Weller PA, Guioli S, Goodfellow PN.

Ann N Y Acad Sci. 1996 Jun 8;785:137-49. Review. No abstract available.

PMID:
8702120
14.

A high-resolution whole genome radiation hybrid map of human chromosome 17q22-q25.3 across the genes for GH and TK.

Foster JW, Schafer AJ, Critcher R, Spillett DJ, Feakes RW, Walter MA, Dominguez-Steglich M, Guioli S, Brook JD, Goodfellow PN.

Genomics. 1996 Apr 15;33(2):185-92.

PMID:
8660966
15.

The role of SOX9 in autosomal sex reversal and campomelic dysplasia.

Schafer AJ, Dominguez-Steglich MA, Guioli S, Kwok C, Weller PA, Stevanovic M, Weissenbach J, Mansour S, Young ID, Goodfellow PN, et al.

Philos Trans R Soc Lond B Biol Sci. 1995 Nov 29;350(1333):271-7; discussion 277-8.

PMID:
8570691
16.

Mutations in SOX9, the gene responsible for Campomelic dysplasia and autosomal sex reversal.

Kwok C, Weller PA, Guioli S, Foster JW, Mansour S, Zuffardi O, Punnett HH, Dominguez-Steglich MA, Brook JD, Young ID, et al.

Am J Hum Genet. 1995 Nov;57(5):1028-36.

17.

Mutations in the DAX-1 gene give rise to both X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism.

Muscatelli F, Strom TM, Walker AP, Zanaria E, Récan D, Meindl A, Bardoni B, Guioli S, Zehetner G, Rabl W, et al.

Nature. 1994 Dec 15;372(6507):672-6.

PMID:
7990958
18.

An unusual member of the nuclear hormone receptor superfamily responsible for X-linked adrenal hypoplasia congenita.

Zanaria E, Muscatelli F, Bardoni B, Strom TM, Guioli S, Guo W, Lalli E, Moser C, Walker AP, McCabe ER, et al.

Nature. 1994 Dec 15;372(6507):635-41.

PMID:
7990953
19.

Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related gene.

Foster JW, Dominguez-Steglich MA, Guioli S, Kwok C, Weller PA, Stevanović M, Weissenbach J, Mansour S, Young ID, Goodfellow PN, et al.

Nature. 1994 Dec 8;372(6506):525-30.

PMID:
7990924
20.

A dosage sensitive locus at chromosome Xp21 is involved in male to female sex reversal.

Bardoni B, Zanaria E, Guioli S, Floridia G, Worley KC, Tonini G, Ferrante E, Chiumello G, McCabe ER, Fraccaro M, et al.

Nat Genet. 1994 Aug;7(4):497-501.

PMID:
7951319
21.

Functional disomy of Xp22-pter in three males carrying a portion of Xp translocated to Yq.

Bardoni B, Floridia G, Guioli S, Peverali G, Anichini C, Cisternino M, Casalone R, Danesino C, Fraccaro M, Zuffardi O, et al.

Hum Genet. 1993 May;91(4):333-8.

PMID:
8099057
22.

Kallmann syndrome gene on the X and Y chromosomes: implications for evolutionary divergence of human sex chromosomes.

Incerti B, Guioli S, Pragliola A, Zanaria E, Borsani G, Tonlorenzi R, Bardoni B, Franco B, Wheeler D, Ballabio A, et al.

Nat Genet. 1992 Dec;2(4):311-4.

PMID:
1303285
23.

Kallmann syndrome due to a translocation resulting in an X/Y fusion gene.

Guioli S, Incerti B, Zanaria E, Bardoni B, Franco B, Taylor K, Ballabio A, Camerino G.

Nat Genet. 1992 Aug;1(5):337-40.

PMID:
1302031
24.

A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules.

Franco B, Guioli S, Pragliola A, Incerti B, Bardoni B, Tonlorenzi R, Carrozzo R, Maestrini E, Pieretti M, Taillon-Miller P, Brown CJ, Willard HF, Lawrence C, Graziella Persico M, Camerino G, Ballabio A.

Nature. 1991 Oct 10;353(6344):529-36.

PMID:
1922361
25.

Probe St35-239 (DXYS64) reveals homology between the distal ends of Xq and Yq.

Pedicini A, Camerino G, Avarello R, Guioli S, Zuffardi O.

Genomics. 1991 Oct;11(2):482-3. No abstract available.

PMID:
1769668
26.

A deletion map of the human Yq11 region: implications for the evolution of the Y chromosome and tentative mapping of a locus involved in spermatogenesis.

Bardoni B, Zuffardi O, Guioli S, Ballabio A, Simi P, Cavalli P, Grimoldi MG, Fraccaro M, Camerino G.

Genomics. 1991 Oct;11(2):443-51.

PMID:
1769656
27.

X-linked Charcot-Marie-Tooth disease. A linkage study in a large family by using 12 probes of the pericentromeric region.

Mostacciuolo ML, Müller E, Fardin P, Micaglio GF, Bardoni B, Guioli S, Camerino G, Danieli GA.

Hum Genet. 1991 May;87(1):23-7.

PMID:
1674715
28.

Two families of low-copy-number repeats are interspersed on Xp22.3: implications for the high frequency of deletions in this region.

Ballabio A, Bardoni B, Guioli S, Basler E, Camerino G.

Genomics. 1990 Oct;8(2):263-70.

PMID:
2249849
29.

Close linkage of probe p212 (DXS178) to X-linked agammaglobulinemia.

Guioli S, Arveiler B, Bardoni B, Notarangelo LD, Panina P, Duse M, Ugazio A, Oberlé I, de Saint Basile G, Mandel JL, et al.

Hum Genet. 1989 Dec;84(1):19-21.

PMID:
2575070
30.

Cytogenetic and molecular analysis of an unbalanced translocation (X;7) (q28;p15) in a dysmorphic girl.

Caiulo A, Bardoni B, Camerino G, Guioli S, Minelli A, Piantanida M, Crosato F, Dalla Fior T, Maraschio P.

Hum Genet. 1989 Dec;84(1):51-4.

PMID:
2558067
31.

A highly conserved sequence on the short arm of chromosome 7 detects multiple polymorphisms.

Bardoni B, Guioli S, Maserati E, Maraschio P, Camerino G.

Hum Genet. 1988 Dec;81(1):23-5.

PMID:
2904403
32.

Isolation and characterization of a family of sequences dispersed on the human X chromosome.

Bardoni B, Guioli S, Raimondi E, Heilig R, Mandel JL, Ottolenghi S, Camerino G.

Genomics. 1988 Jul;3(1):32-8.

PMID:
2851539

Supplemental Content

Loading ...
Support Center