Results 151 to 160 of about 254,310 (345)

CRISPR Screening Reveals a Novel Role for FOXH1 in Regulating Pluripotency of Porcine Embryonic Stem Cells

Advanced Science, EarlyView.
This study performs dual CRISPR screens in pEPSCs. Fitness screening identifies essential genes for viability, while FACS‐based screening uncovers core pluripotency factors. It highlights FOXH1 as a key regulator that maintains the stem cell state through a dual‐action mechanism: preserving pluripotency by enhancing chromatin accessibility and ...
Peng Su, Linhui Wu, Delong Li, Wenting Song, Dagang Tao, Liang Liu, Qi Wang, Manxin Gao, Tian Xu, Xin Liu, Shengsong Xie, Xia Zhang, Jilong Zhou, Yi‐Liang Miao   +13 more
wiley   +1 more source

SIZE AND MORPHOGENESIS IN THE BUD OF BOTRYLLUS

, 1941
N. J. Berrill
openalex   +2 more sources

Morphogenesis of the palate in normal human embryos with special emphasis on the mechanisms involved [PDF]

, 1967
Alphonse R. Burdi, Kathleen Faist
openalex   +1 more source

EVOLUTIONARY MORPHOGENESIS [PDF]

Evolution, 1967
openaire   +2 more sources

Decreasing the Cost of Morphing in Adaptive Morphogenetic Robots

Advanced Intelligent Systems, EarlyView.
Shape‐morphing propulsive limbs enhance locomotion across land‐to‐water transitions, but prior designs rely on thermally responsive components, coupling performance to environmental temperature. This study introduces a pressure‐responsive mechanism that reduces morphing energy costs, enables rapid transitions, and minimizes failure modes.
Luis A. Ramirez, Robert Baines, Bilige Yang, Rebecca Kramer‐Bottiglio   +3 more
wiley   +1 more source

Studies on the Morphogenesis of the Slime Mould, <i>Dictyostelium discoideum</i>

, 1955
Ikuo Takeuchi, Masashi Tazawa
openalex   +2 more sources

Some Observations on the Ultrastructure and Morphogenesis of Photoreceptors [PDF]

, 1960
E. De Robertis
openalex   +1 more source

Chromosome 3q22.2‐q26.2 Interstitial Deletion in a Patient With Wisconsin Syndrome, Blepharophimosis‐Ptosis‐Epicanthus Inversus Syndrome, Dandy‐Walker Malformation, Pierre Robin Sequence, and Recurrent Infections

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Wisconsin syndrome is a very rare genetic condition characterized by coarse facies, prominent nasal tip, bushy high arched/upsweeping eyebrows, and a full/everted lower lip. Deletion of chromosome 3q24q25 region is considered critical for its manifestation.
Pankaj Prasun, Sonja Henry, Vivek Balasubramaniam   +2 more
wiley   +1 more source

Neuroaxonal Dystrophy With Osteopetrosis Associated With a Novel Biallelic Nonsense Homozygous Variant in BORCS5

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Neuroaxonal dystrophy (NAD) with osteopetrosis syndrome (OMIM # 600329) was first reported in a consanguineous Moroccan Jewish family. However, to date, no genetic variant has been linked to this disease. We report on sibs, born to consanguineous Pakistani parents identified prenatally with cerebral ventriculomegaly and agenesis of the corpus ...
Yael Fisher, Orli Greenberg, Patrick Shannon, Andrea Staines, Bobbi McGivern, Melanie Patricia Napier, David Chitayat   +6 more
wiley   +1 more source

Electron Microscopical Study of the Morphogenesis of Collagen Fibers

, 1958
Mitsuhiko Nishikawa
openalex   +2 more sources