Results 81 to 90 of about 502 (138)

Escherichia coli CrfC Protein, a Nucleoid Partition Factor, Localizes to Nucleoid Poles via the Activities of Specific Nucleoid-Associated Proteins

Frontiers in Microbiology, 2019
The Escherichia coli CrfC protein is an important regulator of nucleoid positioning and equipartition. Previously we revealed that CrfC homo-oligomers bind the clamp, a DNA-binding subunit of the DNA polymerase III holoenzyme, promoting colocalization of
Saki Taniguchi, Kazutoshi Kasho, Shogo Ozaki, Tsutomu Katayama   +3 more
doaj   +1 more source

The constraining process depends on MatP and ZapB.

, 2012
(A–D) Travelled distance of different markers in strains deleted for zapB, deleted for segment rins2 and zapB, and in wt strain. The representation is the same as in Figure 2. (A) strain with a deletion of zapB (markers Ori-3, NSR-2, Right-2 (R2), Ter-3,
Olivier Espéli (37459), Axel Thiel (170052), Michèle Valens (37458), Isabelle Vallet-Gely (170057), Frédéric Boccard (37460)   +4 more
core   +1 more source

ANALISIS SEKUEN EKSON 5 GEN MATP PADA PENDERITA OCULOCUTANEOUS ALBINISM (OCA) DI YOGYAKARTA

, 2011
Albinism is a genetic disorder caused by mutation of the gen encode melanin (the skin, hair, and eye pigments). Clinically, albinism is divided into 2 types, those are Ocular Albinism (OA) and Oculocutaneous Albinism (OCA).
, Dr. Niken Satuti Nur Handayani, M.Sc., , ETI ARINASTITI   +1 more
core  

The Symmetrical Wave Pattern of Base-Pair Substitution Rates across the Escherichia coli Chromosome Has Multiple Causes

mBio, 2019
Mutation accumulation experiments followed by whole-genome sequencing have revealed that, for several bacterial species, the rate of base-pair substitutions (BPSs) is not constant across the chromosome but varies in a wave-like pattern that is ...
Brittany A. Niccum, Heewook Lee, Wazim MohammedIsmail, Haixu Tang, Patricia L. Foster   +4 more
doaj   +1 more source

MUTASI MISSENSE (P.374PHE/LEU) PADA EKSON 5 GEN MATP, PENYEBAB OCULOCUTANEOUS ALBINISM TIPE 4 (OCA4) DI WONOSOBO, JAWA TENGAH [PDF]

, 2013
ABSTRAK Albinisme merupakan kelainan genetik autosomal resesif  berupa gangguan sintesis melanin yang terjadi pada manusia. Albinisme dibagi menjadi dua kelompok besar, yaitu Ocular Albinism (OA) dan Oculocutaneous Albinism (OCA).
Nur Handayani, Niken Satuti, Sukmawati, Feri, Pratiwi, Rarastoeti   +2 more
core  

Schematic models of MATP function as a putative transporter in regulating melanosomal pH in normal and OCA4 conditions.

, 2015
Under normal conditions, MATP elevates the melanosomal pH by functioning as a transporter using a proton gradient. Under this condition, copper can bind to tyrosinase (Cu-Tyrosinase), resulting in active tyrosinase.
Jinhyuk Bhin (623259), Daehee Hwang (113308), Misun Shin (752146), Ai-Young Lee (623263), Yeon-Ju Nam (752147), Eun-Gyung Cho (208159), Bum-Ho Bin (226967), Dong-Hwa Choi (623261), Seung Ha Yang (623260), Tae Ryong Lee (433037), Dong Wook Shin (176902)   +10 more
core   +1 more source

Polymorphisms Detected in the Tyrosinase and MATP (SLC45A2) Genes Did Not Explain Coat Colour Dilution in a Sample of Alpaca (Vicugna pacos) [PDF]

, 2009
The molecular basis of inheritance of alpaca fibre colour is poorly understood. However, colour dilution genes are anticipated to be causing a major effect on alpaca fibre colour.
R. Cransberg (23349910), Kylie Munyard (6865661)   +1 more
core   +1 more source

Museo de de Artes y Tradiciones Populares “Luis Repetto Málaga”: una propuesta de plan museológico en pos de su revalorización

Illapa
El presente artículo tiene como objetivo destacar los aportes de la propuesta de plan museológico para el Museo de Artes y Tradiciones Populares «Luis Repetto Málaga» (MATP), y reflexionar sobre su potencial rol como espacio referente de las artes ...
Beatriz López Infantas, Claudio Mendoza Castro   +1 more
doaj   +1 more source

MUTASI MISSENSE (P.374PHE/LEU) PADA EKSON 5 GEN MATP, PENYEBAB OCULOCUTANEOUS ALBINISM TIPE 4 (OCA4) DI WONOSOBO, JAWA TENGAH [PDF]

, 2011
Albinisme merupakan kelainan genetik autosomal resesif berupa gangguan sintesis melanin yang terjadi pada manusia. Albinisme dibagi menjadi dua kelompok besar, yaitu Ocular Albinism (OA) dan Oculocutaneous Albinism (OCA).
Nur Handayani, Niken Satuti, Pratiwi, R. (Rarastoeti), Sukmawati, Feri, Satuti Nur Handayani, Niken, Sukmawati, F. (Feri), Pratiwi, Rarastoeti   +5 more
core  

Polymorphisms detected in the tyrosinase and matp (slc45a2) genes did not explain coat colour dilution in a sample of Alpaca (Vicugna pacos)

, 2011
The molecular basis of the inheritance of alpaca fibre colour is poorly understood. It is likely that colour dilution is having an influence on alpaca fibre colour, with all primarily pheomelanic animals differing mainly in their total melanin ...
Cransberg, R., Kylie Ann Munyard, Rhys Cransberg, Munyard, Kylie   +3 more
core   +2 more sources