✦ LIBER ✦

Identification of the Gene Whose Mutation Leads to the Appearance of Recessive Lethal Germlings inArabidopsis thaliana

✍ Scribed by O. A. Ogarkova; A. A. Tomilov; N. B. Tomilova; V. A. Tarasov

Publisher: Springer
Year: 2005
Tongue: English
Weight: 65 KB
Volume: 36
Category: Article
ISSN: 1062-3604
DOI: 10.1007/s11174-005-0028-4

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Identification of the gene whose mutatio

Identification of the gene whose mutation leads to hypocoptyl tropism inArabidopsis thaliana

✍ O. A. Ogarkova; A. A. Tomilov; N. B. Tomilova; V. A. Tarasov 📂 Article 📅 2005 🏛 SP MAIK Nauka/Interperiodica 🌐 English ⚖ 58 KB

Identification of the gene whose mutatio

Identification of the gene whose mutation leads to the morphological changes in the hypocotyl ofArabidopsis thaliana

✍ O. A. Ogarkova; A. A. Tomilov; N. B. Tomilova; G. V. Pogorelko; V. A. Tarasov 📂 Article 📅 2005 🏛 SP MAIK Nauka/Interperiodica 🌐 English ⚖ 83 KB

The dependence of the frequency of reces

The dependence of the frequency of recessive lethal and vital mutations inArabidopsis thaliana(L.)Heynh.on the concentration of N-nitroso-N-methylurea

✍ Milena Riesová-Kučerová 📂 Article 📅 1969 🏛 Springer Netherlands 🌐 English ⚖ 512 KB

Identification of two new mutations in T

Identification of two new mutations in TRPS 1 gene leading to the tricho-rhino-phalangeal syndrome type I and III

✍ Maria Piccione; Marcello Niceta; Vincenzo Antona; Antonella Di Fiore; Filomena C 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 200 KB 👁 1 views

Mutation screening of the fibrillin-1 (F

Mutation screening of the fibrillin-1 (FBN1) gene in 76 unrelated patients with Marfan syndrome or Marfanoid features leads to the identification of 11 novel and three previously reported mutations

✍ Kathrin Rommel; Matthias Karck; Axel Haverich; Jörg Schmidtke; Mine Arslan-Kirch 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 38 KB

Mutations in the gene encoding fibrillin-1 (FBN1) cause Marfan syndrome (MFS) and other related connective tissue disorders. In this study we performed SSCP to analyze all 65 exons of the FBN1 gene in 76 patients presenting with classical MFS or related phenotypes. We report 7 missense mutations, 3

Mutation analysis of the HOX paralogous

Mutation analysis of the HOX paralogous 4–13 genes in children with acute lymphoid malignancies: Identification of a novel germline mutation of HOXD4 leading to a partial loss-of-function

✍ Virginie van Scherpenzeel Thim; Sophie Remacle; Jacques Picard; Guy Cornu; Franç 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 331 KB 👁 1 views

Communicated by