Results
|
|
141.
|
|
|
|
142.
|
Gain-of-function mutations in the phosphatidylserine synthase 1 (PTDSS1) gene cause Lenz-Majewski syndrome. [electronic resource] by
- Sousa, Sérgio B
- Jenkins, Dagan
- Chanudet, Estelle
- Tasseva, Guergana
- Ishida, Miho
- Anderson, Glenn
- Docker, James
- Ryten, Mina
- Sa, Joaquim
- Saraiva, Jorge M
- Barnicoat, Angela
- Scott, Richard
- Calder, Alistair
- Wattanasirichaigoon, Duangrurdee
- Chrzanowska, Krystyna
- Simandlová, Martina
- Van Maldergem, Lionel
- Stanier, Philip
- Beales, Philip L
- Vance, Jean E
- Moore, Gudrun E
Producer: 20140304
In:
Nature genetics vol. 46
Availability: No items available.
|
|
|
143.
|
|
|
|
144.
|
|
|
|
145.
|
|
|
|
146.
|
|
|
|
147.
|
|
|
|
148.
|
|
|
|
149.
|
|
|
|
150.
|
|
|
|
151.
|
Nutrient shortage triggers the hexosamine biosynthetic pathway via the GCN2-ATF4 signalling pathway. [electronic resource] by
- Chaveroux, Cédric
- Sarcinelli, Carmen
- Barbet, Virginie
- Belfeki, Sofiane
- Barthelaix, Audrey
- Ferraro-Peyret, Carole
- Lebecque, Serge
- Renno, Toufic
- Bruhat, Alain
- Fafournoux, Pierre
- Manié, Serge N
Producer: 20180426
In:
Scientific reports vol. 6
Availability: No items available.
|
|
|
152.
|
|
|
|
153.
|
Genetic defects in mtDNA-encoded protein translation cause pediatric, mitochondrial cardiomyopathy with early-onset brain disease. [electronic resource] by
- Kamps, Rick
- Szklarczyk, Radek
- Theunissen, Tom E
- Hellebrekers, Debby M E I
- Sallevelt, Suzanne C E H
- Boesten, Iris B
- de Koning, Bart
- van den Bosch, Bianca J
- Salomons, Gajja S
- Simas-Mendes, Marisa
- Verdijk, Rob
- Schoonderwoerd, Kees
- de Coo, Irenaeus F M
- Vanoevelen, Jo M
- Smeets, Hubert J M
Producer: 20181226
In:
European journal of human genetics : EJHG vol. 26
Availability: No items available.
|
|
|
154.
|
|
|
|
155.
|
|
|
|
156.
|
|
|
|
157.
|
|
|
|
158.
|
|
|
|
159.
|
|
|
|
160.
|
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