Works matching IS 09646906 AND DT 2006 AND VI 15 AND IP 17

Results: 10

Evolutionary insights into the high worldwide prevalence of MBL2 deficiency alleles.
Published in:
Human Molecular Genetics, 2006, v. 15, n. 17, p. 2650, doi. 10.1093/hmg/ddl193
By:
- Verdu, Paul;
- Barreiro, Luis B.;
- Patin, Etienne;
- Gessain, Antoine;
- Cassar, Olivier;
- Kidd, Judith R.;
- Kidd, Kenneth K.;
- Behar, Doron M.;
- Froment, Alain;
- Heyer, Evelyne;
- Sica, Lucas;
- Casanova, Jean-Laurent;
- Abel, Laurent;
- Quintana-Murci, Lluís
Publication type:
Article
Allelic mRNA expression of X-linked monoamine oxidase a (MAOA) in human brain: dissection of epigenetic and genetic factors.
Published in:
Human Molecular Genetics, 2006, v. 15, n. 17, p. 2636, doi. 10.1093/hmg/ddl192
By:
- Pinsonneault, Julia K.;
- Papp, Audrey C.;
- Sadée, Wolfgang
Publication type:
Article
Abnormal CpG island methylation occurs during in vitro differentiation of human embryonic stem cells.
Published in:
Human Molecular Genetics, 2006, v. 15, n. 17, p. 2623, doi. 10.1093/hmg/ddl188
By:
- Shen, Yin;
- Chow, Janet;
- Wang, Zunde;
- Fan, Guoping
Publication type:
Article
Cooperative sequence modules determine replication initiation sites at the human β-globin locus.
Published in:
Human Molecular Genetics, 2006, v. 15, n. 17, p. 2613, doi. 10.1093/hmg/ddl187
By:
- Wang, Lixin;
- Lin, Chii Mei;
- Lopreiato, Joseph O.;
- Aladjem, Mirit I.
Publication type:
Article
Skeletal muscle repair in a mouse model of nemaline myopathy.
Published in:
Human Molecular Genetics, 2006, v. 15, n. 17, p. 2603, doi. 10.1093/hmg/ddl186
By:
- Sanoudou, Despina;
- Corbett, Mark A.;
- Han, Mei;
- Ghoddusi, Majid;
- Nguyen, Mai-Anh T.;
- Vlahovich, Nicole;
- Hardeman, Edna C.;
- Beggs, Alan H.
Publication type:
Article
In vivo function of the orphan nuclear receptor NR2E3 in establishing photoreceptor identity during mammalian retinal development.
Published in:
Human Molecular Genetics, 2006, v. 15, n. 17, p. 2588, doi. 10.1093/hmg/ddl185
By:
- Cheng, Hong;
- Aleman, Tomas S.;
- Cideciyan, Artur V.;
- Khanna, Ritu;
- Jacobson, Samuel G.;
- Swaroop, Anand
Publication type:
Article
Pathogenetic role of the deafness-related M34T mutation of Cx26.
Published in:
Human Molecular Genetics, 2006, v. 15, n. 17, p. 2569, doi. 10.1093/hmg/ddl184
By:
- Bicego, Massimiliano;
- Beltramello, Martina;
- Melchionda, Salvatore;
- Carella, Massimo;
- Piazza, Valeria;
- Zelante, Leopoldo;
- Bukauskas, Feliksas F.;
- Arslan, Edoardo;
- Cama, Elona;
- Pantano, Sergio;
- Bruzzone, Roberto;
- D'Andrea, Paola;
- Mammano, Fabio
Publication type:
Article
DAPK1 variants are associated with Alzheimer's disease and allele-specific expression.
Published in:
Human Molecular Genetics, 2006, v. 15, n. 17, p. 2560, doi. 10.1093/hmg/ddl178
By:
- Li, Yonghong;
- Grupe, Andrew;
- Rowland, Charles;
- Nowotny, Petra;
- Kauwe, John S.K.;
- Smemo, Scott;
- Hinrichs, Anthony;
- Tacey, Kristina;
- Toombs, Timothy A.;
- Kwok, Shirley;
- Catanese, Joseph;
- White, Thomas J.;
- Maxwell, Taylor J.;
- Hollingworth, Paul;
- Abraham, Richard;
- Rubinsztein, David C.;
- Brayne, Carol;
- Wavrant-De Vrièze, Fabienne;
- Hardy, John;
- O'Donovan, Michael
Publication type:
Article
The ERK1/2 pathway modulates nuclear PTEN-mediated cell cycle arrest by cyclin D1 transcriptional regulation.
Published in:
Human Molecular Genetics, 2006, v. 15, n. 17, p. 2553, doi. 10.1093/hmg/ddl177
By:
- Chung, Ji-Hyun;
- Ostrowski, Michael C.;
- Romigh, Todd;
- Minaguchi, Takeo;
- Waite, Kristin A.;
- Eng, Charis
Publication type:
Article
The MELAS mutations 3946 and 3949 perturb the critical structure in a conserved loop of the ND1 subunit of mitochondrial complex I.
Published in:
Human Molecular Genetics, 2006, v. 15, n. 17, p. 2543, doi. 10.1093/hmg/ddl176
By:
- Kervinen, Marko;
- Hinttala, Reetta;
- Helander, Heli M.;
- Kurki, Sari;
- Uusimaa, Johanna;
- Finel, Moshe;
- Majamaa, Kari;
- Hassinen, Ilmo E.
Publication type:
Article